Staff Profile

Roles and Responsibilities

Sir James Spence Professor of Child Health

Professor in Paediatric Immunology and Haematopoietic Stem Cell Transplantation

Honorary Consultant Paediatric Immunologist, Great North Children's Hospital

Director of the Northern Deanery Academic Foundation Pragramme 

Designated Individual – Newcastle upon Tyne Foundation Hospital Trust Tissue Bank

Lecturer in Immunology for CSIM2, CSIM3, MRes Biomolecular Sciences

Qualifications

MBChB, MD, MRCP, FRCPCH, DCH, Dip Med Sci

Memberships

European Society of Immunodeficiency Clinical Working Party Chair

European Society of Immunodeficiency Inborn Errors Working Party Member

European Society of Immunodeficiency

European Group for Blood and Marrow Transplantation

British Society of Immunology

British Paediatric Allergy, Immunology and Infectious Diseases Group

RCPCH Academic Regional Representative (Northern)

Member RCPCH Academic Executive Committee

Paediatric member on BMT-CRG

CIBMTR Co-Chair of Primary Immune Deficiencies, Inborn Errors of Metabolism and other NMMD Working Committee

Research Interests

Polysaccharide Antibody Responses
VDJ recombination in Primary Immunodeficiency
Immune Reconstitution post Bone Marrow Transplantation
Immunodeficiency in DiGeorge syndrome

ECP treatment of acute GvHD, central and peripheral tolerance

Endothelial activation syndromes post transplant

Other Expertise

Defects in Non homologous end joining and human disease

Current Work

DNA repair disorders and Immunodeficiency:

Ongoing collaborations with Penny Jeggo at the University of Sussex, examining DNA repair disorders and their contribution to human immunodeficienies.

Development of central and peripheral tolerance during ECP treatment of acute GvHD

Role of endothelial cell damage in idiopathic pneumonitis post HSCT

Investigating health status and quality of life in patients with autosomal dominant hyper IgE syndrome

Research Roles

Prinicipal investigator

Undergraduate Research student supervisor

Postgraduate Research student supervisor

Postgraduate Research student assessor

Postgraduate Research student examiner

Postgraduate Supervision

I am currently supervising 5 PhD student, 1 MD student

I have supervised 8 PhDs, 6 MDs, and 16 Masters, and have been examiner for 24 doctoral theses, 4 of which were overseas.

Esteem Indicators.

Over 310 articles on primary immunodeficiency, treatment and outcomes.

Over 30 chapters on primary immunodeficiency in major text books

Co-author on several disease-specific consensus statements and management guidelines

Sub-section editor on PID of the Orphanet Journal of Rare Diseases

Associate Editor for Frontiers in Immunology

Editorial Board Member of Journal of Clinical Immunology, Frontiers in Paediatrics, Clinical Immunology

I sit on the Scientific Advisory Board for:

• The Chronic Granulomatous Disorder Society
• The HyperIgM Foundation 
• The Job’s Syndrome Foundation

I am paediatric representative on the UKPIN Registry Steering group.

I chair the Information, Training and Consent sub-committee of Public Health England SCID Newborn screening working group

I am an occasional advisor to NICE.

Funding

Leukaemia Research Fund -2009 Investigating Early Haematopoietic Development in Ligase IV and XLF Deficient Patients using induced pluripotent stem cells. £165,845 (with LM Lako).

The Oddfellows (Bubble Foundation) - 2009 Measuring Antibody Quality in Premature Babies Following Vaccination £18486

SPARKS – 2009 A study to determine the antibody response to Haemophilus Influenzae type b and Neisseria Meningitidis type C vaccines in UK preterm and term infants immunised with Prevenar conjugate heptavalent pneumococcal vaccine. £18973

Tiny Lives – 2008. Measuring pneumococcal serotypes in nasal swabs from Premature Babies Following Vaccination £16200

Bubble Foundation UK – 2008. Continuing studies into a New Gene Causing Omenn’s Syndrome variant of T Cell Negative Severe Combined immunodeficiency (with AJ Cant). £26,881

Bubble Foundation UK – 2008. Data collection and analysis co-ordinator for paediatric bone marrow transplantation unit (with AJ Cant). £8,833

Bubble Foundation UK – 2008. Continuing studies into a New Gene Causing Omenn’s Syndrome variant of T Cell Negative Severe Combined immunodeficiency (with AJ Cant). £39,785

Bubble Foundation UK – 2007 - 2008. Research development and support officer. £21,000

Kay Kendall Leukaemia Fund – 2008-2009.
Identification of non-HLA gene polymorphisms association with post transplant complications following bone marrow transplantation using a genome -wide scanning methodology. (with PG Middleton) £121027

Undergraduate Teaching

I teach immunology to the 2nd year medical students (CSIM 2)
I teach immunology to the medical students on the accelerated medical degree

I teach immunology to the 4th year medical students (CSIM 3) and I am the Theme Leader for 'Immunology in Medicine'

Postgraduate Teaching

I give 2 lectures on two MRes courses on immunodeficiency, bone marrow transplantation and gene therapy :
MRes Transplantation Sciences
Mres Immunobiology

• Articles

  • Vallee TC, Glasmacher JS, Buchner H, Arkwright PD, Behrends U, Bondarenko A, Browning MJ, Buchbinder D, Cattoni A, Chernyshova L, Ciznar P, Cole T, Czogala W, Dueckers G, Edgar JDM, Erbey F, Fasth A, Ferrua F, Formankova R, Gambineri E, Gennery AR, Goldman FD, Gonzalez-Granado LI, Heilmann C, Heiskanen-Kosma T, Juntti H, Kainulainen L, Kanegane H, Karaca NE, Sebnem Kilic S, Klein C, Koltan S, Kondratenko I, Meyts I, Nasrullayeva GM, Notarangelo LD, Pasic S, Pellier I, Pignata C, Misbah S, Schulz A, Segundo GR, Shcherbina A, Slatter M, Sokolic R, Soler-Palacin P, Stepensky P, van Montfrans JM, Ryhanen S, Wolska-Kusnierz B, Ziegler JB, Zhao X, Aiuti A, Ochs HD, Albert MH. Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival. Blood 2024, epub ahead of print.
  • Lum SH, Albert MH, Gilbert P, Sirait T, Algeri M, Muratori R, Fournier B, Laberko A, Karakukcu M, Unal E, Ayas M, Yadav SP, Fisgin T, Elfeky R, Fernandes J, Faraci M, Cole T, Schulz A, Meisel R, Zecca M, Ifversen M, Biffi A, Diana J-S, Vallee T, Giardino S, Ersoy GZ, Moshous D, Gennery AR, Balashov D, Bonfim C, Locatelli F, Lankester A, Neven B, Slatter M. Outcomes of HLA-mismatched HSCT with TCRαβ/CD19 depletion or post-HSCT cyclophosphamide for inborn errors of immunity. Blood 2024, epub ahead of print.
  • Tsilifis C, Spegarova JS, Good R, Griffin H, Engelhardt KR, Graham S, Hughes S, Arkwright PD, Hambleton S, Gennery AR. Omenn Syndrome in Two Infants with Different Hypomorphic Variants in Janus Kinase 3. Journal of Clinical Immunology 2024, 44(4), 98.
  • Triaille C, Rao NM, Rice GI, Seabra L, Sutherland FJH, Bondet V, Duffy D, Gennery AR, Fournier B, Bader-Meunier B, Troedson C, Cleary G, Buso H, Dalby-Payne J, Ranade P, Jansen K, De Somer L, Fremond M-L, Chavan PP, Wong M, Dale RC, Wouters C, Quartier P, Khubchandani R, Crow YJ. Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System Inflammation. Journal of Clinical Immunology 2024, 44(8), 185.
  • Tsilifis C, Speckmann C, Lum SH, Fox TA, Soler AM, Mozo Y, Corral D, Ewins A-M, Hague R, Oikonomopoulou C, Kalwak K, Drabko K, Wynn R, Morris EC, Elcombe S, Bigley V, Lougaris V, Malagola M, Hauck F, Sedlacek P, Laberko A, Tjon JML, Buddingh EP, Wehr C, Grimbacher B, Gennery AR, Lankester AC, Albert MH, Neven B, Slatter MA. Hematopoietic stem cell transplantation for CTLA-4 insufficiency across Europe: A European Society for Blood and Marrow Transplantation Inborn Errors Working Party study. Journal of Allergy and Clinical Immunology 2024, epub ahead of print.
  • Cleminson JS, Thomas J, Stewart CJ, Campbell D, Gennery A, Embleton ND, Koglmeier J, Wong T, Spruce M, Berrington JE. Gut microbiota and intestinal rehabilitation: A prospective childhood cohort longitudinal study of short bowel syndrome (the MIRACLS study): Study protocol. BMJ Open Gastroenterology 2024, 11(1), e001450.
  • Fisher AJ, Carby M, Thompson R, Parmar J, Alaloul M, Santhanakrishnan K, Hancock H, Wason J, Grayling M, Hasenfuss J, Lally J, Gennery A, Exley C, Lordan J, Bradley P, Flinn A, Bardgett M, White M, Goudie N, Phillipson J, Kershaw A, Smith H, Russell S, Vale L, Chadwick T, Bryant A, Bevin-Nicholls A, Frisby L, Johnson R. Extracorporeal Photopheresis (ECP) in the Treatment of Chronic Lung Allograft Dysfunction (CLAD): a prospective, multicentre, open-label, randomised controlled trial studying the addition of ECP to standard care in the treatment of bilateral lung transplant patients with CLAD (E-CLAD UK). BMJ Open Respiratory Research 2024, 11(1), e001995.
  • van der Made C, Kersten S, Chorin O, Engelhardt KR, Ramakrishnan G, Griffin H, van der Loeff IS, Venselaar H, Rothschild AR, Segev M, Schuurs-Hoeijmakers JHM, Mantere T, Essers R, Esteki MZ, Avital AL, Loo PS, Simons A, Pfundt R, Warris A, Seyger MM, van de Veerdonk F, Netea MG, Slatter MA, Flood T, Gennery AR, Simon AM, Lev A, Frizinsky S, Barel O, van der Burg M, Somech R, Hambleton S, Henriet SRVS, Hoischen A. Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit b- type 10 in six infants with SCID-Omenn syndrome. American Journal of Human Genetics 2024, (ePub ahead of Print).
  • Kreins AY, Dhalla F, Flinn AM, Howley E, Ekwall O, Villa A, Staal FJT, Anderson G, Gennery AR, Hollander GA, Davies EG, Burns SO, Carrabba M, Gardulf A, Haerynck F, Hauck F, Jandus P, Meyts I, Klocperk A, Neven B, Pac M, Pergent M, Sediva A, Soler-Palacin P, Velcheva M, Warnatz K. European Society for Immunodeficiencies guidelines for the management of patients with congenital athymia. Journal of Allergy and Clinical Immunology 2024, epub ahead of print.
  • Berghuis D, Mehyar LS, Abu-Arja R, Albert MH, Barnum JL, von Bernuth H, Elfeky R, Lewalle P, Laberko A, Ghosh S, Slatter MA, Weemaes CMR, Yesilipek A, Sirait T, Neven B, Gennery AR, Lankester AC. Allogeneic Hematopoietic Stem Cell Transplantation in Immunodeficiency—Centromeric Instability—Facial Dysmorphism (ICF) Syndrome: an EBMT/ESID Inborn Errors Working Party Study. Journal of Clinical Immunology 2024, 44(8), 182.
  • Lum SH, James B, Ottaviano G, Ewins A-M, Patrick K, Ali S, Carpenter B, Silva J, Tewari S, Furness C, Thomas A, Shenton G, Bonney D, Moppett J, Hambleton S, Gennery AR, Amrolia P, Gibson B, Hough R, Rao K, Slatter M, Wynn R. Alemtuzumab, Dual Graft-versus-Host Disease Prophylaxis, and Lower CD3+ T Cell Doses Equalize Rates of Acute and Chronic Graft-versus-Host Disease in Pediatric Patients Receiving Allogeneic Hematopoietic Stem Cell Transplantation with Matched Unrelated Donor Peripheral Blood Stem Cells or Bone Marrow Grafts. Transplantation and Cellular Therapy 2024, 30(3), 314.e1-314.e12.
  • Chen R, Lukianova E, van der Loeff IS, Spegarova JS, Willet JDP, James KD, Ryder EJ, Griffin H, IJspeert H, Gajbhiye A, Lamoliatte F, Marin-Rubio JL, Woodbine L, Lemos H, Swan DJ, Pintar V, Sayes K, Ruiz-Morales ER, Eastham S, Dixon D, Prete M, Prigmore E, Jeggo P, Boyes J, Mellor A, Huang L, van der Burg M, Engelhardt KR, Stray-Pedersen A, Erichsen HC, Gennery AR, Trost M, Adams DJ, Anderson G, Lorenc A, Trynka G, Hambleton S. NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome. Science Immunology 2024, 9(95), eade5705.
  • Mehta P, Tsilifis C, Lum SH, Slatter MA, Hambleton S, Owens S, Williams E, Flood T, Gennery AR, Nademi Z. Outcome of Second Allogeneic HSCT for Patients with Inborn Errors of Immunity: Retrospective Study of 20 Years’ Experience. Journal of Clinical Immunology 2023, 43, 1812–1826.
  • Offor UT, Hollis P, Ognjanovic M, Parry G, Khushnood A, Long HM, Gennery AR, Bacon CM, Simmonds J, Reinhardt Z, Bomken S. Immunology of THymectomy And childhood CArdiac transplant (ITHACA): protocol for a UK-wide prospective observational cohort study to identify immunological risk factors of post-transplant lymphoproliferative disease (PTLD) in thymectomised children. BMJ Open 2023, 13(10), e079582.
  • Schuetz C, Gerke J, Ege M, Walter J, Kusters M, Worth A, Kanakry JA, Dimitrova D, Wolska-Kusnierz B, Chen K, Unal E, Karakukcu M, Pashchenko O, Leiding J, Kawai T, Amrolia PJ, Berghuis D, Buechner J, Buchbinder D, Cowan MJ, Gennery AR, Gungor T, Heimall J, Miano M, Meyts I, Morris EC, Riviere J, Sharapova SO, Shaw PJ, Slatter M, Honig M, Veys P, Fischer A, Cavazzana M, Moshous D, Schulz A, Albert MH, Puck JM, Lankester AC, Notarangelo LD, Neven B. Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT. Blood 2023, 141(7), 713–724.
  • Ramanathan S, Veramendi-Espinoza L, Shillitoe B, Flinn A, Owens S, Williams E, Emonts M, Hambleton S, Burton-Fanning S, Waugh S, Flood T, Gennery AR, Slatter M, Nademi Z. Haploidentical CD3+ TCR αβ/CD19+–depleted HSCT for MHC class II deficiency and persistent SARS-CoV-2 pneumonitis. Journal of Allergy and Clinical Immunology 2023, 2(1), 101-104.
  • Israni M, Nicholson B, Mahlaoui N, Obici L, Rossi-Semerano L, Lachmann H, Hayward G, Avramovic MZ, Guffroy A, Dalm V, Rimmer R, Solis L, Villar C, Gennery AR, Skeffington S, Nordin J, Warnatz K, Korganow A-S, Anton J, Cattalini M, Amin T, Berg S, Soler-Palacin P, Burns SO, Campbell M, Wouters C, Meyts I, van der Werff ten Bosch JE, Goffin L, Ogunjimi B, Gilliaux O, Kelecic J, Jelusic M, Fingerhutova S, Sediva A, Herlin T, Seppanen Mikko RJ, Aalto K, Ritterbusch H, Insalaco A, Moschese V, Plebani A, Cimaz R, Canessa C, Dellepiane RM, Carrabba M, Barzaghi F, van Laar JAM, Wulffraat NM, Marques L, Carreras C, Sanchez-Manubens J, Alsina L, Seoane Reula ME, Mendez-Echevarria A, Gonzales-Granado LI, Santamaria M, Neth O, Ekwall O, Brodszki O, Hague H, Devlin LA, Brogan P, Arkwright PD, Riordan A, McCann L, McDermott E, Faust SN, Carne E. Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey. Journal of Clinical Immunology 2023, 43, 206-216.
  • Ramanathan S, Lum SH, Nademi Z, Carruthers K, Watson H, Flood T, Owens S, Williams E, Hambleton S, Gennery AR, Slatter M. CD3+TCRαβ/CD19+-Depleted Mismatched Family or Unrelated Donor Salvage Stem Cell Transplantation for Graft Dysfunction in Inborn Errors of Immunity. Transplantation and Cellular Therapy 2023, 29(8), 513.e1-513.e9.
  • Nishimura A, Uppuluri R, Raj R, Swaminathan VV, Cheng Y, Abu-Arja RF, Fu B, Laberko A, Albert MH, Hauck F, Bucciol G, Bigley V, Elcombe S, Kharya G, Pronk CJH, Wehr C, Neven B, Warnatz K, Meyts I, Morio T, Gennery AR, Kanegane H. An International Survey of Allogeneic Hematopoietic Cell Transplantation for X-Linked Agammaglobulinemia. Journal of Clinical Immunology 2023, 43, 1827–1839.
  • Tsilifis C, Torppa T, Williams EJ, Albert MH, Hauck F, Soncini E, Kang E, Malech H, Schuetz C, von Bernuth H, Slatter MA, Gennery AR. Allogeneic HSCT for Symptomatic Female X-linked Chronic Granulomatous Disease Carriers. Journal of Clinical Immunology 2023, 43, 1964-1973.
  • Wolf J, Alfred A, Gennery AR, New HV, Scarisbrick J, Griffin J. UK national survey of anticoagulation in extra-corporeal photopheresis—Is it time for a UK consensus statement?. Transfusion Medicine 2022, 32(1), 77-81.
  • Jeyaratnam J, Faraci M, Gennery AR, Drabko K, Algeri M, Morimoto A, Sirait T, Lankester AC, Albert M, Neven B, Frenkel J. The efficacy and safety of allogeneic stem cell transplantation in Mevalonate Kinase Deficiency. Pediatric Rheumatology 2022, 20(1), 56.
  • Tsilifis C, Lum SH, Nademi Z, Hambleton S, Flood TJ, Williams EJ, Owens S, Abinun M, Cant AJ, Slatter MA, Gennery AR. TCRαβ-Depleted Haploidentical Grafts Are a Safe Alternative to HLA-Matched Unrelated Donor Stem Cell Transplants for Infants with Severe Combined Immunodeficiency. Journal of Clinical Immunology 2022, 42, 851-858.
  • van Rees DJ, Brinkhaus M, Klein B, Verkuijlen P, Tool ATJ, Schornagel K, Treffers LW, van Houdt M, Kater AP, Vidarsson G, Gennery AR, Kuijpers TW, van Bruggen R, Matlung HL, van den Berg TK. Sodium stibogluconate and CD47-SIRPa blockade overcome resistance of anti-CD20–opsonized B cells to neutrophil killing. Blood Advances 2022, 6(7), 2156-2166.
  • Blom M, Zetterstrom RH, Stray-Pedersen A, Gilmour K, Gennery AR, Puck JM, van der Burg M. Recommendations for uniform definitions used in newborn screening for severe combined immunodeficiency. Journal of Allergy and Clinical Immunology 2022, 149(4), 1428-1436.
  • Tomomasa D, Booth C, Bleesing JJ, Isoda T, Kobayashi C, Koike K, Taketani T, Sawada A, Tamura A, Marsh RA, Morio T, Gennery AR, Kanegane H. Preemptive hematopoietic cell transplantation for asymptomatic patients with X-linked lymphoproliferative syndrome type 1. Clinical Immunology 2022, 237, 108993.
  • Yang L, Booth C, Speckmann C, Seidel MG, Worth AJJ, Kindle G, Lankester AC, Grimbacher B, Sediva A, Neven B, Hauck F, Warnatz K, Pac M, Carrabba M, Palacin P, Jandus P, Gardulf A, Mahlaoui N, Pergent M, Schutz C, Sharapova S, Vassilios L, Candotti F, Volpi S, Gennery AR, Seppanen MRJ, Morris EC, Burns SO. Phenotype, genotype, treatment, and survival outcomes in patients with X-linked inhibitor of apoptosis deficiency. Journal of Allergy and Clinical Immunology 2022, 150(2), 456-466.
  • Shields AM, Anantharachagan A, Arumugakani G, Baker K, Bahal S, Baxendale H, Bermingham W, Bhole M, Boules E, Bright P, Chopra C, Cliffe L, Cleave B, Dempster J, Devlin L, Dhalla F, Diwakar L, Drewe E, Duncan C, Dziadzio M, Elcombe S, Elkhalifa S, Gennery A, Ghanta H, Goddard S, Grigoriadou S, Hackett S, Hayman G, Herriot R, Herwadkar A, Huissoon A, Jain R, Jolles S, Johnston S, Khan S, Laffan J, Lane P, Leeman L, Lowe DM, Mahabir S, Lochlainn DJM, McDermott E, Misbah S, Moghaddas F, Morsi H, Murng S, Noorani S, O'Brien R, Patel S, Price A, Rahman T, Seneviratne S, Shrimpton A, Stroud C, Thomas M, Townsend K, Vaitla P, Verma N, Williams A, Burns SO, Savic S, Richter AG. Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK. Clinical and Experimental Immunology 2022, 209(3), 247-258.
  • Dimitrova D, Nademi Z, Maccari ME, Ehl S, Uzel G, Tomoda T, Okano T, Imai K, Carpenter B, Ip W, Rao K, Worth AJJ, Laberko A, Mukhina A, Neven B, Moshous D, Speckmann C, Warnatz K, Wehr C, Abolhassani H, Aghamohammadi A, Bleesing JJ, Dara J, Dvorak CC, Ghosh S, Kang HJ, Markelj G, Modi A, Bayer DK, Notarangelo LD, Schulz A, Garcia-Prat M, Soler-Palacin P, Karakukcu M, Yilmaz E, Gambineri E, Menconi M, Masmas TN, Holm M, Bonfim C, Prando C, Hughes S, Jolles S, Morris EC, Kapoor N, Koltan S, Paneesha S, Steward C, Wynn R, Duffner U, Gennery AR, Lankester AC, Slatter M, Kanakry JA. International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome. Journal of Allergy and Clinical Immunology 2022, 149(1), P410-421.E7.
  • Albert MH, Sirait T, Eikema DJ, Bakunina K, Wehr C, Suarez F, Fox ML, Mahlaoui N, Gennery AR, Lankester AJ, Beier R, Bernardo ME, Bigley V, Lindemans CA, OBurns S, Carpenter B, Dybko J, Gungor T, Hauck F, Lum SH, Balashov D, Meisel R, Moshous D, Schulz A, Speckmann C, Slatter MA, Strahm B, Uckan-Cetinkaya D, Meyts I, Vallee TC, Wynn R, Neven B, Morris EC, EBMT IEWP, ESID. Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study. Blood 2022, 140(14), 1635-1649.
  • Lankester AC, Neven B, Mahlaoui N, von Asmuth EGJ, Courteille V, Alligon M, Albert MH, Serra IB, Bader P, Balashov D, Beier R, Bertrand Y, Blanche S, Bordon V, Bredius RG, Cant A, Cavazzana M, Diaz-de-Heredia C, Dogu F, Ehlert K, Entz-Werle N, Fasth A, Ferrua F, Ferster A, Formankova R, Friedrich W, Gonzalez-Vicent M, Gozdzik J, Gungor T, Hoenig M, Ikinciogullari A, Kalwak K, Kansoy S, Kupesiz A, Lanfranchi A, Lindemans CA, Meisel R, Michel G, Miranda NAA, Moraleda J, Moshous D, Pichler H, Rao K, Sedlacek P, Slatter M, Soncini E, Speckmann C, Sundin M, Toren A, Vettenranta K, Worth A, Yesilipek MA, Zecca M, Porta F, Schulz A, Veys P, Fischer A, Gennery AR. Hematopoietic cell transplantation in severe combined immunodeficiency: The SCETIDE 2006-2014 European cohort. Journal of Allergy and Clinical Immunology 2022, 149(5), 1744-1754.e8.
  • Ghimenton E, Flinn A, Lum SH, Leahy TR, Nademi Z, Owens S, Williams E, Flood T, Hambleton S, Slatter M, Gennery AR. Hematopoietic Cell Transplantation for Adenosine Deaminase Severe Combined Immunodeficiency—Improved Outcomes in the Modern Era. Journal of Clinical Immunology 2022, 42, 819-826.
  • Arnold DE, Chellapandian D, Parikh S, Mallhi K, Marsh RA, Heimall JR, Grossman D, Chitty-Lopez M, Murguia-Favela L, Gennery AR, Boulad F, Arbuckle E, Cowan MJ, Dvorak CC, Griffith LM, Haddad E, Kohn DB, Notarangelo LD, Pai S-Y, Puck JM, Pulsipher MA, Torgerson T, Kang EM, Malech HL, Leiding JW. Granulocyte Transfusions in Patients with Chronic Granulomatous Disease Undergoing Hematopoietic Cell Transplantation or Gene Therapy. Journal of Clinical Immunology 2022, 42, 1026–1035.
  • Marsh RA, Hebert K, Kim S, Dvorak CC, Aquino VM, Baker KS, Chellapandian D, Davila Saldana B, Duncan CN, Eckrich MJ, Georges GE, Olson TS, Pulsipher MA, Shenoy S, Stenger E, Lugt MV, Yu LC, Gennery AR, Eapen M. Comparison of hematopoietic cell transplant conditioning regimens for hemophagocytic lymphohistiocytosis disorders. Journal of Allergy and Clinical Immunology 2022, 149(3), 1097-1104.e2.
  • Van der Velden FJS, Gennery A, Emonts M. Biomarkers for diagnosing febrile illness in immunocompromised children: a systematic review of the literature. Frontiers in Pediatrics 2022, 10, 828569.
  • Tsilifis C, Schim van der Loeff I, Williams E, Owens S, Powell S, Gennery AR, Slatter M. BCG lymphadenitis: a potential complication of immune reconstitution following haematopoietic stem cell transplant. Archives of Diseases in Childhood: Education and Practice Edition 2022, 107(4), 274-275.
  • Machowicz R, Suarez F, Wiktor-Jedrzejczak W, Eikema D-J, de Wreede LC, Blok H-J, Isaksson C, Einsele H, Poire X, van Dorp S, Nikolousis E, Johansson J-E, Kobbe G, Zecca M, Arnold R, Gerbitz A, Finke J, Diez-Martin JL, Bonifazi F, McQuaker G, Lenhoff S, Rohrlich P-S, Theobald M, Ljungman P, Collin M, Albert MH, Ehninger G, Carlson K, Halaburda K, Lehmberg K, Schonland S, Yakoub-Agha I, Gennery AR, Lankester AC, Kroger N. Allogeneic hematopoietic stem cell transplantation for adult HLH: a retrospective study by the chronic malignancies and inborn errors working parties of EBMT. Bone Marrow Transplantation 2022, 57, 817-823.
  • Slatter MA, Gennery AR. Advances in the treatment of severe combined immunodeficiency. Clinical Immunology 2022, 242, 109084.
  • Kitko CL, Abdel-Azim H, Carpenter PA, Dalle J-H, Diaz-de-Heredia C, Gaspari S, Gennery AR, Handgretinger R, Lawitschka A. A Prospective, Multicenter Study of Closed-System Extracorporeal Photopheresis for Children with Steroid-Refractory Acute Graft-versus-Host Disease. Transplantation and Cellular Therapy 2022, 28(5), 261.e1-261.e7.
  • Offor UT, Bacon CM, Roberts J, Powell J, Brodlie M, Wood K, Windebank KP, Flett J, Hewitt T, Rand V, Hasan A, Parry G, Gennery AR, Reinhardt Z, Bomken S. Transplantation For Congenital Heart Disease Is Associated With An Increased Risk Of Epstein-Barr Virus-Related Post-Transplant Lymphoproliferative Disorder In Children. Journal of Heart and Lung Transplantation 2021, 35(5), 24-32.
  • Flinn AM, Ehrlich A, Roberts C, Wang XN, Chou J, Gennery AR. Thymopoiesis, Alterations in Dendritic Cells and Tregs, and Reduced T Cell Activation in Successful Extracorporeal Photopheresis Treatment of GVHD. Journal of Clinical Immunology 2021, 41, 1016-1030.
  • Ferrua F, Bortolomai I, Fontana E, Di Silvestre D, Rigoni R, Marcovecchio GE, Draghici E, Brambilla F, Castiello MC, Delfanti G, Moshous D, Picard C, Taghon T, Bordon V, Schulz AS, Schuetz C, Giliani S, Soresina A, Gennery AR, Signa S, Davila Saldana BJ, Delmonte OM, Notarangelo LD, Roifman CM, Poliani PL, Uva P, Mauri PL, Villa A, Bosticardo M. Thymic Epithelial Cell Alterations and Defective Thymopoiesis Lead to Central and Peripheral Tolerance Perturbation in MHCII Deficiency. Frontiers in Immunology 2021, 12, 669943.
  • Tsilifis C, Moreira D, Marques L, Neves E, Slatter MA, Gennery AR. Stem cell transplantation as treatment for major histocompatibility class I deficiency. Clinical Immunology 2021, 229, 108801.
  • Tsilifis C, Freeman AF, Gennery AR. STAT3 Hyper-IgE Syndrome-an Update and Unanswered Questions. Journal of Clinical Immunology 2021, 41, 864-880.
  • Lum SH, Elfeky R, Achini FR, Margarit-Soler A, Cinicola B, Perez-Heras I, Nademi Z, Flood T, Cheetham T, Worth A, Qasim W, Amin R, Rao K, Chiesa R, Bredius RGM, Amrolia P, Abinun M, Hambleton S, Veys P, Gennery AR, Lankester A, Slatter M. Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary Immunodeficiency. Journal of Clinical Immunology 2021, 41, 171-184.
  • Radwan N, Nademi Z, Lum SH, Flood T, Abinun M, Owens S, Williams E, Gennery AR, Hambleton S, Slatter MA. Outcome of Hematopoietic Stem Cell Transplantation in patients with Mendelian Susceptibility to Mycobacterial Diseases. Journal of Clinical Immunology 2021, 41, 1774-1780.
  • Laberko A, Burlakov V, Maier S, Abinun M, Skinner R, Kozlova A, Suri D, Lehmberg K, Muller I, Balashov D, Novichkova G, Holzinger D, Gennery AR, Shcherbina A. HSCT is effective in patients with PSTPIP1-associated myeloid-related proteinemia inflammatory (PAMI) syndrome. Journal of Allergy and Clinical Immunology 2021, 148(1), 250-255.e1.
  • Perez-Heras I, Tsilifis C, Slatter MA, Brynjolfsson SF, Haraldsson A, Gennery AR. HSCT in two brothers with CGD arising from mutations in CYBC1 corrects the defect in neutrophil function. Clinical Immunology 2021, 229, 108799.
  • Harrison SC, Tsilifis C, Slatter MA, Nademi Z, Worth A, Veys P, Ponsford MJ, Jolles S, Al-Herz W, Flood T, Cant AJ, Doffinger R, Barcenas-Morales G, Carpenter B, Hough R, Haraldsson Á, Heimall J, Grimbacher B, Abinun M, Gennery AR. Hematopoietic Stem Cell Transplantation Resolves the Immune Deficit Associated with STAT3-Dominant-Negative Hyper-IgE Syndrome. Journal of Clinical Immunology 2021, 41, 934-943.
  • Wolska-Kusnierz B, Pastorczak A, Fendler W, Wakulinska A, Dembowska-Baginska B, Heropolitanska-Pliszka E, Piatosa B, Pietrucha B, Kalwak K, Ussowicz M, Pieczonka A, Drabko K, Lejman M, Koltan S, Gozdzik J, Styczynski J, Fedorova A, Miakova N, Deripapa E, Kostyuchenko L, Krenova Z, Hlavackova E, Gennery AR, Sykora K-W, Ghosh S, Albert MH, Balashov D, Eapen M, Svec P, Seidel MG, Kilic SS, Tomaszewska A, Wiesik-Szewczyk E, Kreins A, Greil J, Buechner J, Lund B, Gregorek H, Chrzanowska K, Mlynarski W. Hematopoietic stem cell transplantation positively affects the natural history of cancer in Nijmegen breakage syndrome. Clinical Cancer Research 2021, 27(2), 575-584.
  • Shillitoe BMJ, Ponsford M, Slatter MA, Evans J, Struik S, Cosgrove M, Doull I, Jolles S, Gennery AR. Haematopoietic Stem Cell Transplant for Norovirus-Induced Intestinal Failure in X-linked Agammaglobulinemia. Journal of Clinical Immunology 2021, 41, 1574-1581.
  • Knobler R, Arenberger P, Arun A, Assaf C, Bagot M, Berlin G, Bohbot A, Calzavara-Pinton P, Child F, Cho A, French LE, Gennery AR, Gniadecki R, Gollnick HPM, Guenova E, Jaksch P, Jantschitsch C, Klemke C, Ludvigsson J, Papadavid E, Scarisbrick J, Schwarz T, Stadler R, Wolf P, Zic J, Zouboulis C, Zuckermann A, Greinix H. European dermatology forum: Updated guidelines on the use of extracorporeal photopheresis 2020 – Part 2. Journal of the European Academy of Dermatology and Venereology 2021, 35(1), 27-49.
  • Shields AM, Burns SO, Savic S, Richter AG, Anantharachagan A, Arumugakani G, Baker K, Bahal S, Bermingham W, Bhole M, Boules E, Bright P, Burns S, Cleave B, Dempster J, Devlin L, Dhalla F, Drewe E, Duncan C, Dziadzio M, Elkhalifa S, Gennery A, Goddard S, Grigoriadou S, Hayman G, Herwadkar A, Huissoon A, Jain R, Jolles S, Johnston S, Leeman L, Mahabir S, MacLochlainn D, McDermott E, Misbah S, Morsi H, Murng S, Noorani S, O'Brien R, Patel S, Price A, Richter A, Seneviratne S, Shields A, Shrimpton A, Stroud C, Vaitla P, Verma N. COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience. Journal of Allergy and Clinical Immunology 2021, 147(3), 870-875.
  • Ponsford MJ, Shillitoe BMJ, Humphreys IR, Gennery AR, Jolles S. COVID-19 and X-linked agammaglobulinemia (XLA) - insights from a monogenic antibody deficiency. Current Opinion in Allergy and Clinical Immunology 2021, 21(6), 525-534.
  • Meyts I, Bucciol G, Quinti I, Neven B, Fischer A, Seoane E, Lopez-Granados E, Gianelli C, Robles-Marhuenda A, Jeandel P-Y, Paillard C, Sankaran VG, Demirdag YY, Lougaris V, Aiuti A, Plebani A, Milito C, Dalm VA, Guevara-Hoyer K, Sanchez-Ramon S, Bezrodnik L, Barzaghi F, Gonzalez-Granado LI, Hayman GR, Uzel G, Mendonca LO, Agostini C, Spadaro G, Badolato R, Soresina A, Vermeulen F, Bosteels C, Lambrecht BN, Keller M, Mustillo PJ, Abraham RS, Gupta S, Ozen A, Karakoc-Aydiner E, Baris S, Freeman AF, Yamazaki-Nakashimada M, Scheffler-Mendoza S, Espinosa-Padilla S, Gennery AR, Jolles S, Espinosa Y, Poli MC, Fieschi C, Hauck F, Cunningham-Rundles C, Mahlaoui N, Warnatz K, Sullivan KE, Tangye SG. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study. Journal of Allergy and Clinical Immunology 2021, 147(2), 520-531.
  • Tsilifis C, Slatter M, Cordeiro AI, Hambleton S, Engelhardt KR, Griffin H, Gennery AR, Neves JF. Congenital nephrotic syndrome in IL7Rα-SCID: A rare feature of maternofetal graft-versus-host disease. Journal of Allergy and Clinical Immunology: In Practice 2021, 9(11), 4151-4153.E1.
  • Bakhtiar S, Salzmann-Manrique E, Blok H-J, Eikema D-J, Hazelaar S, Ayas M, Toren A, Goldstein G, Moshous D, Locatelli F, Merli P, Michel G, Ozturk G, Schulz A, Heilmann C, Ifversen M, Wynn RF, Aleinikova O, Bertrand Y, Tbakhi A, Veys P, Karakukcu M, Kupesiz A, Ghavamzadeh A, Handgretinger R, Unal E, Perez-Martinez A, Gokce M, Porta F, Aksu T, Karasu G, Badell I, Ljungman P, Skorobogatova E, Yesilipek A, Zuckerman T, Bredius RRG, Stepensky P, Shadur B, Slatter M, Gennery AR, Albert MH, Bader P, Lankester A. Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type I and III. Blood Advances 2021, 5(1), 262-273.
  • Slatter MA, Gennery AR. Update on DNA-Double Strand Break Repair Defects in Combined Primary Immunodeficiency. Current Allergy and Asthma Reports 2020, 20, 57.
  • Gennery AR. The challenges presented by haematopoietic stem cell transplantation in children with primary immunodeficiency. British Medical Bulletin 2020, 135(1), 4-15.
  • Felber M, Steward CG, Kentouche K, Fasth A, Wynn RF, Zeilhofer U, Haunerdinger V, Volkmer B, Prader S, Gruhn B, Ehl S, Lehmberg K, Muller D, Gennery AR, Albert MH, Hauck F, Rao K, Veys P, Hassan M, Lankester AC, Schmid JP, Hauri-Hohl MM, Gungor T. Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosis. Blood Advances 2020, 4(9), 1998-2010.
  • Lum SH, Selvarajah S, Deya-Martinez A, McNaughton P, Sobh A, Waugh S, Burton-Fanning S, Newton L, Gandy J, Nademi Z, Owens S, Williams E, Emonts M, Flood T, Cant A, Abinun M, Hambleton S, Gennery AR, Slatter M. Outcome of autoimmune cytopenia after hematopoietic cell transplantation in primary immunodeficiency. Journal of Allergy and Clinical Immunology 2020, 146(2), 406-416.
  • Elfeky R, Lucchini G, Lum SH, Ottaviano G, Builes N, Nademi Z, Battersby A, Flood T, Owens S, Cant AJ, Young H, Greener S, Walsh P, Kavanagh D, Annavarapu S, Rao K, Amrolia P, Chiesa R, Worth A, Booth C, Skinner R, Doncheva B, Standing J, Gennery AR, Qasim W, Slatter M, Veys P. New Insights Into Risk Factors for Transplant-Associated Thrombotic Microangiopathy in Pediatric HSCT. Blood Advances 2020, 4(11), 2418-2429.
  • Deya-Martinez A, Flinn AM, Gennery AR. Neonatal thymectomy in children—accelerating the immunologic clock?. Journal of Allergy and Clinical Immunology 2020, 146(2), 236-243.
  • Tesch VK, Abolhassani H, Shadur B, Zobel J, Mareika Y, Sharapova S, Karakoc-Aydiner E, Riviere JG, Garcia-Prat M, Moes N, Haerynck F, Gonzales-Granado LI, Santos Perez JL, Mukhina A, Shcherbina A, Aghamohammadi A, Hammarstrom L, Dogu F, Haskologlu S, Ikinciogullari AI, Kostel Bal S, Baris S, Kilic SS, Karaca NE, Kutukculer N, Girschick H, Kolios A, Keles S, Uygun V, Stepensky P, Worth A, van Montfrans JM, Peters AMJ, Meyts I, Adeli M, Marzollo A, Padem N, Khojah AM, Chavoshzadeh Z, Avbelj Stefanija M, Bakhtiar S, Florkin B, Meeths M, Gamez L, Grimbacher B, Seppanen MRJ, Lankester A, Gennery AR, Seidel MG. Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score. Journal of Allergy and Clinical Immunology 2020, 145(5), 1452-1463.
  • Lum SH, Anderson C, McNaughton P, Engelhardt K, MacKenzie B, Watson H, Al-Mousa H, Al-Herz W, Al-Saud B, Mohammed R, ALZahrani D, Alghamdi HA, Goronfolah L, Nademi Z, Habibolla S, Flinn AM, Shillitoe B, Owens S, Williams E, Emonts M, Hambleton S, Abinun M, Flood T, Cant A, Gennery AR, Slatter M. Improved transplant survival and long-term disease outcome in children with MHC class II deficiency. Blood 2020, 135(12), 954-973.
  • Prunotto G, Offor UT, Samarasinghe S, Wynn R, Vora A, Carpenter B, Gowdy C, McHugh K, Windebank KP, Rovelli AM, Slatter MA, Gennery AR, Veys P, Bacon CM, Bomken S, Lucchini G. HSCT provides effective treatment for lymphoproliferative disorders in children with primary immunodeficiency. Journal of Allergy and Clinical Immunology 2020, 146(2), 447-450.
  • Ponsford MJ, Clark J, Mock J, Abinun M, Carne E, El-Shanawany T, Williams PE, Choudhury A, Freeman AF, Gennery AR, Jolles S. Hematopoietic Stem Cell Transplantation and Vasculopathy Associated With STAT3-Dominant-Negative Hyper-IgE Syndrome. Frontiers in Pediatrics 2020, 8, 575.
  • Chan AY, Leiding JW, Liu X, Logan BR, Burroughs LM, Allenspach EJ, Skoda-Smith S, Uzel G, Notarangelo LD, Slatter M, Gennery AR, Smith AR, Pai S-Y, Jordan MB, Marsh RA, Cowan MJ, Dvorak CC, Craddock JA, Prockop SE, Chandrakasan S, Kapoor N, Buckley RH, Parikh S, Chellapandian D, Oshrine BR, Bednarski JJ, Cooper MA, Shenoy S, Davila Saldana BJ, Forbes LR, Martinez C, Haddad E, Shyr DC, Chen K, Sullivan KE, Heimall J, Wright N, Bhatia M, Cuvelier GDE, Goldman FD, Meyts I, Miller HK, Seidel MG, Vander Lugt MT, Bacchetta R, Weinacht KG, Andolina JR, Caywood E, Chong H, de la Morena MT, Aquino VM, Shereck E, Walter JE, Dorsey MJ, Seroogy CM, Griffith LM, Kohn DB, Puck JM, Pulsipher MA, Torgerson TR. Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey. Frontiers in Immunology 2020, 11, 239.
  • Richards S, Gennery AR, Davies EG, Wong M, Shaw PJ, Peake J, Fraser C, Gray P, Brothers S, Sinclair J, Prestidge T, Preece K, Quinn P, Ramachandran S, Loh R, McLean-Tooke A, Mitchell R, Cole T. Diagnosis and management of severe combined immunodeficiency in Australia and New Zealand. Journal of Paediatrics and Child Health 2020, 56(10), 1508-1513.
  • Rigoni R, Fontana E, Dobbs K, Marrella V, Taverniti V, Maina V, Facoetti A, D'Amico G, Al-Herz W, Cruz-Munoz ME, Schuetz C, Gennery AR, Garabedian EK, Giliani S, Draper D, Dbaibo G, Geha RS, Meyts I, Tousseyn T, Neven B, Moshous D, Fischer A, Schulz A, Finocchi A, Kuhns DB, Fink DL, Lionakis MS, Swamydas M, Guglielmetti S, Alejo J, Myles IA, Pittaluga S, Notarangelo LD, Villa A, Cassani B. Cutaneous barrier leakage and gut inflammation drive skin disease in Omenn syndrome. Journal of Allergy and Clinical Immunology 2020, 146(5), 1165-1179.e11.
  • Wolfs TFW, Attarbaschi A, Balduzzi A, Bernardo ME, Bomken S, Borkhardt A, Bourquin JP, Dufour C, Gennery A, Grainger J, Hasle H, Hrusak O, Izraeli S, Mechinaud F, Trka J, Vormoor J. COVID-19 - Impact on childhood haematology patients. Hemasphere 2020, 4(5), e465.
  • Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery AR, Kawasaki Y, Ichishima J, Osawa M, Nihira H, Shiba T, Tanaka T, Chrabieh M, Bigio B, Hur H, Itan Y, Liang Y, Okada S, Izawa K, Nishikomori R, Ohara O, Heike T, Abel L, Puel A, Saito MK, Casanova J-L, Hagiwara M, Yasumi T. Rescue of recurrent deep intronic mutation underlying cell type–dependent quantitative NEMO deficiency. Journal of Clinical Investigation 2019, 129(2), 583-597.
  • Tirosh I, Yamazaki Y, Frugoni F, Ververs FA, Allenspach EJ, Zhang Y, Burns S, Al-Herz W, Noroski L, Walter JE, Gennery AR, van der Burg M, Notarangelo LD, Lee YN. Recombination activity of human recombination-activating gene 2 (RAG2) mutations and correlation with clinical phenotype. Journal of Allergy and Clinical Immunology 2019, 143(2), 726-735.
  • Chiesa R, Standing JF, Winter R, Nademi Z, Chu J, Pinner D, Kloprogge F, McLellen S, Amrolia PJ, Rao K, Lucchini G, Silva J, Ciocarlie O, Lazareva A, Gennery AR, Doncheva B, Cant AJ, Hambleton S, Flood T, Rogerson E, Devine K, Prunty H, Heales S, Veys P, Slatter M. Proposed Therapeutic Range of Treosulfan in Reduced Toxicity Pediatric Allogeneic Hematopoietic Stem Cell Transplant Conditioning: Results From a Prospective Trial. Clinical Pharmacology and Therapeutics 2019, 108(2), 264-273.
  • Verrinder AE, Marsden JLS, Slatter MA, McDonald L, Bacon CM, Majo J, Gennery AR. Late relapse of primary hemophagocytic lymphohistiocytosis after hematopoietic stem cell transplantation: a consequence of low-level chimerism from a carrier donor?. Immunologic Research 2019, 67, 261-264.
  • Nademi Z, Wynn RF, Slatter M, Hughes SM, Bonney D, Qasim W, Latour S, Truck J, Patel S, Abinun M, Flood T, Hambleton S, Cant AJ, Gennery AR, Arkwright PD. Hematopoietic stem cell transplantation for cytidine triphosphate synthase 1 (CTPS1) deficiency. Bone Marrow Transplantation 2019, 54(1), 130-133.
  • Aydin SE, Freeman AF, Al-Herz W, Al-Mousa HA, Arnaout RK, Aydin RC, Barlogis V, Belohradsky BH, Bonfim C, Bredius RG, Chu JI, Ciocarlie OC, Dogu F, Gaspar HB, Geha RS, Gennery AR, Hauck F, Hawwari A, Hickstein DD, Hoenig M, Ikinciogullari A, Klein C, Kumar A, Ifversen MRS, Matthes S, Metin A, Neven B, Pai S-Y, Parikh SH, Picard C, Renner ED, Sanal O, Schulz AS, Schuster F, Shah NN, Shereck EB, Slatter MA, Su HC, van Montfrans J, Woessmann W, Ziegler JB, Albert MH. Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency. Journal of Allergy and Clinical Immunology: In Practice 2019, 7(3), 848-855.
  • Battersby AC, Braggins H, Pearce MS, McKendrick F, Campbell M, Burns S, Cale CM, Goldblatt D, Gennery AR. Health-Related Quality of Life and Emotional Health in X-Linked Carriers of Chronic Granulomatous Disease in the United Kingdom. Journal of Clinical Immunology 2019, 39, 195-199.
  • Bucciol G, Nicholas SK, Calvo PL, Cant A, Edgar JDM, Espanol T, Ferrua F, Galicchio M, Gennery AR, Hadzic N, Hanson IC, Kusminsky G, Lange A, Lanternier F, Mahlaoui N, Moshous D, Nademi Z, Neven B, Oleastro M, Porta F, Quarello P, Silva M, Slatter MA, Soncini E, Stefanowicz M, Tandoi F, Teisseyre M, Torgerson TR, Veys P, Weinacht KG, Wolska-Kusnierz B, Pirenne J, de la Morena MT, Meyts I. Combined liver and hematopoietic stem cell transplantation in patients with X-linked hyper-IgM syndrome. Journal of Allergy and Clinical Immunology 2019, 143(5), 1952-1956.e6.
  • Greco R, Labopin M, Badoglio M, Veys P, Silva JMF, Abinun M, Gualandi F, Bornhauser M, Ciceri F, Saccardi R, Lankester A, Alexander T, Gennery AR, Bader P, Farge D, Snowden JA. Allogeneic HSCT for Autoimmune Diseases: A Retrospective Study From the EBMT ADWP, IEWP, and PDWP Working Parties. Frontiers in Immunology 2019, 10, 1570.
  • Slatter MA, Rao K, Abd Hamid IJ, Nademi Z, Chiesa R, Elfeky R, Pearce MS, Amrolia P, Worth A, Flood T, Abinun M, Hambleton S, Qasim W, Gaspar HB, Cant AJ, Gennery AR, Veys P. Treosulfan and Fludarabine Conditioning for Hematopoietic Stem Cell Transplantation in Children with Primary Immunodeficiency: UK Experience. Biology of Blood and Marrow Transplantation 2018, 24(3), 529-536.
  • Flinn AM, Roberts CF, Slatter MA, Skinner R, Robson H, Lawrence J, Guest J, Gennery AR. Thymopoiesis following HSCT; a retrospective review comparing interventions for aGVHD in a pediatric cohort. Clinical Immunology 2018, 193, 33-37.
  • Shillitoe B, Bangs C, Guzman D, Gennery AR, Longhurst HJ, Slatter M, Edgar DM, Thomas M, Worth A, Huissoon A, Arkwright PD, Jolles S, Bourne H, Alachkar H, Savic S, Kumararatne DS, Patel S, Baxendale H, Noorani S, Yong PFK, Waruiru C, Pavaladurai V, Kelleher P, Herriot R, Bernatonienne J, Bhole M, Steele C, Hayman G, Richter A, Gompels M, Chopra C, Garcez T, Buckland M. The United Kingdom Primary Immune Deficiency (UKPID) registry 2012 to 2017. Clinical and Experimental Immunology 2018, 192(3), 284-291.
  • Shah RM, Elfeky R, Nademi Z, Qasim W, Amrolia P, Chiesa R, Rao K, Lucchini G, Silva JMF, Worth A, Barge D, Ryan D, Conn J, Cant AJ, Skinner R, Abd Hamid IJ, Flood T, Abinun M, Hambleton S, Gennery AR, Veys P, Slatter M. T-cell receptor αβ+ and CD19+ cell-depleted haploidentical and mismatched hematopoietic stem cell transplantation in primary immune deficiency. Journal of Allergy and Clinical Immunology 2018, 141(4), 1417-1426.e1.
  • Slack J, Albert MH, Balashov D, Belohradsky BH, Bertaina A, Bleesing J, Booth C, Buechner J, Buckley RH, Ouachee-Chardin M, Deripapa E, Drabko K, Eapen M, Feuchtinger T, Finocchi A, Gaspar HB, Ghosh S, Gillio A, Gonzalez-Granado LI, Grunebaum E, Gungor T, Heilmann C, Helminen M, Higuchi K, Imai K, Kalwak K, Kanazawa N, Karasu G, Kucuk ZY, Laberko A, Lange A, Mahlaoui N, Meisel R, Moshous D, Muramatsu H, Parikh S, Pasic S, Schmid I, Schuetz C, Schulz A, Schultz KR, Shaw PJ, Slatter MA, Sykora K-W, Tamura S, Taskinen M, Wawer A, Wolska-Kusnierz B, Cowan MJ, Fischer A, Gennery AR. Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders. Journal of Allergy and Clinical Immunology 2018, 141(1), 322-328.e10.
  • Belderbos ME, Gennery AR, Dvorak CC, Blok H-J, Eikema D-J, Silva JMF, Veys P, Neven B, Buckley R, Cole T, Cowan MJ, Goebel WS, Hoenig M, Kuo CY, Stiehm ER, Wynn R, Bierings M. Outcome of domino hematopoietic stem cell transplantation in human subjects: An international case series. Journal of Allergy and Clinical Immunology 2018, 142(5), 1628-1631.e4.
  • Unni MNM, Elfeky R, Rao K, Nademi Z, Chiesa R, Amrolia P, Skinner R, Slater O, Worth A, Flood T, Abinun M, Hambleton S, Qasim W, Gaspar HB, Cant AJ, Gennery AR, Veys P, Slatter MA. Non-posttransplant lymphoproliferative disorder malignancy after hematopoietic stem cell transplantation in patients with primary immunodeficiency: UK experience. Journal of Allergy and Clinical Immunology 2018, 141(6), 2319-2321.e1.
  • Ip W, Silva JMF, Gaspar H, Mitra A, Patel S, Rao K, Chiesa R, Amrolia P, Gilmour K, Ahsan G, Slatter M, Gennery AR, Wynn RF, Veys P, Qasim W. Multicenter phase 1/2 application of adenovirus-specific T cells in high-risk pediatric patients after allogeneic stem cell transplantation. Cytotherapy 2018, 20(6), 830-838.
  • Abd Hamid IJ, Slatter MA, McKendrick F, Pearce MS, Gennery AR. Long-Term Health Outcome and Quality of Life Post-HSCT for IL7Rα-, Artemis-, RAG1- and RAG2-Deficient Severe Combined Immunodeficiency: a Single Center Report. Journal of Clinical Immunology 2018, 38(6), 727-732.
  • Barzaghi F, Amaya Hernandez LC, Neven B, Ricci S, Kucuk ZY, Bleesing JJ, Nademi Z, Slatter MA, Ulloa ER, Shcherbina A, Roppelt A, Worth A, Silva J, Aiuti A, Murguia-Favela L, Speckmann C, Carneiro-Sampaio M, Fernandes JF, Baris S, Ozen A, Karakoc-Aydiner E, Kiykim A, Schulz A, Steinmann S, Notarangelo LD, Gambineri E, Lionetti P, Shearer WT, Forbes LR, Martinez C, Moshous D, Blanche S, Fisher A, Ruemmele FM, Tissandier C, Ouachee-Chardin M, Rieux-Laucat F, Cavazzana M, Qasim W, Lucarelli B, Albert MH, Kobayashi I, Alonso L, Diaz De Heredia C, Kanegane H, Lawitschka A, Seo JJ, Gonzalez-Vicent M, Diaz MA, Goyal RK, Sauer MG, Yesilipek A, Kim M, Yilmaz-Demirdag Y, Bhatia M, Khlevner J, Richmond Padilla EJ, Martino S, Montin D, Neth O, Molinos-Quintana A, Valverde-Fernandez J, Broides A, Pinsk V, Ballauf A, Haerynck F, Bordon V, Dhooge C, Garcia-Lloret ML, Bredius RG, Kalwak K, Haddad E, Seidel MG, Duckers G, Pai S-Y, Dvorak CC, Ehl S, Locatelli F, Goldman F, Gennery AR, Cowan MJ, Roncarolo M-G, Bacchetta R. Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study. Journal of Allergy and Clinical Immunology 2018, 141(3), 1036-1049.e5.
  • Forbes LR, Vogel TP, Cooper MA, Castro-Wagner J, Schussler E, Weinacht KG, Plant AS, Su HC, Allenspach EJ, Slatter M, Abinun M, Lilic D, Cunningham-Rundles C, Eckstein O, Olbrich P, Guillerman RP, Patel NC, Demirdag YY, Zerbe C, Freeman AF, Holland SM, Szabolcs P, Gennery A, Torgerson TR, Milner JD, Leiding JW. Jakinibs for the treatment of immune dysregulation in patients with gain-of-function signal transducer and activator of transcription 1 (STAT1) or STAT3 mutations. Journal of Allergy and Clinical Immunology 2018, 142(5), 1665-1669.
  • Ghosh S, Drexler I, Bhatia S, Gennery AR, Borkhardt A. Interleukin-2-inducible T-cell kinase deficiency-new patients, new insight?. Frontiers in Immunology 2018, 9, 979.
  • Cytlak U, Resteu A, Bogaert D, Kuehn HS, Altmann T, Gennery A, Jackson G, Kumanovics A, Voelkerding KV, Prader S, Dullaers M, Reichenbach J, Hill H, Haerynck F, Rosenzweig SD, Collin M, Bigley V. Ikaros family zinc finger 1 regulates dendritic cell development and function in humans. Nature Communications 2018, 9, 1239.
  • Leiding JW, Okada S, Hagin D, Abinun M, Shcherbina A, Balashov DN, Kim VHD, Ovadia A, Guthery SL, Pulsipher M, Lilic D, Devlin LA, Christie S, Depner M, Fuchs S, van Royen-Kerkhof A, Lindemans C, Petrovic A, Sullivan KE, Bunin N, Kilic SS, Arpaci F, Calle-Martin ODL, Martinez-Martinez L, Aldave JC, Kobayashi M, Ohkawa T, Imai K, Iguchi A, Roifman CM, Gennery AR, Slatter M, Ochs HD, Morio T, Torgerson TR. Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations. Journal of Allergy and Clinical Immunology 2018, 141(2), 704-717.e5.
  • Altmann T, Slack J, Slatter MA, O'Brien C, Cant A, Thomas M, Brodlie M, Annavarapu S, Gennery AR. Endothelial cell damage in idiopathic pneumonia syndrome. Bone Marrow Transplantation 2018, 53(4), 515-518.
  • Bigley V, Maisuria S, Cytlak U, Jardine L, Care MA, Green K, Gunawan M, Milne P, Dickinson R, Wiscombe S, Parry D, Doffinger R, Laurence A, Fonseca C, Stoevesandt O, Gennery A, Cant A, Tooze R, Simpson AJ, Hambleton S, Savic S, Doody G, Collin M. Biallelic interferon regulatory factor 8 mutation: A complex immunodeficiency syndrome with dendritic cell deficiency, monocytopenia, and immune dysregulation. Journal of Allergy and Clinical Immunology 2018, 141(6), 2234-2248.
  • Tholouli E, Sturgess K, Dickinson RE, Gennery A, Cant AJ, Jackson G, Lordan J, Hambleton S, Slatter MA, Bigley V, Collin M. In vivo T-depleted reduced intensity transplantation for GATA2-related immune dysfunction. Blood 2018, 131(12), 1383-1387.
  • Yeates L, Slatter MA, Bonanomi S, Lim FLWI, Ong SY, Dalissier A, Barberi W, Shulz A, Duval M, Heilmann C, Willekens A, Hwang WHY, Uderzo C, Bader P, Gennery AR. Use of defibrotide to treat transplant-associated thrombotic microangiopathy: a retrospective study of the Paediatric Diseases and Inborn Errors Working Parties of the European Society of Blood and Marrow Transplantation. Bone Marrow Transplantation 2017, 52, 762-764.
  • Seidel MG, Bohm K, Dogu F, Worth A, Thrasher A, Florkin B, Ikinciogullari A, Peters A, Bakhtiar S, Meeths M, Stepensky P, Meyts I, Sharapova SO, Gamez-Diaz L, Hammarstrom L, Ehl S, Grimbacher B, Gennery AR. Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation. Journal of Allergy and Clinical Immunology 2017, 141(2), 770-775.
  • Alfred A, Taylor PC, Dignan F, El-Ghariani K, Griffin J, Gennery AR, Bonney D, Das-Gupta E, Lawson S, Malladi RK, Douglas KW, Maher T, Guest J, Hartlett L, Fisher AJ, Child F, Scarisbrick JJ. The role of extracorporeal photopheresis in the management of cutaneous T-cell lymphoma, graft-versus-host disease and organ transplant rejection: a consensus statement update from the UK Photopheresis Society. British Journal of Haematology 2017, 177(2), 287-310.
  • Hoenig M, Lagresle-Peyrou C, Pannicke U, Notarangelo LD, Porta F, Gennery AR, Slatter M, Cowan MJ, Stepensky P, Al-Mousa H, Al-Zahrani D, Pai S-Y, Al Herz W, Gaspar HB, Veys P, Oshima K, Imai K, Yabe H, Noroski LM, Wulffraat NM, Sykora K-W, Soler-Palacin P, Muramatsu H, Al Hilali M, Moshous D, Debatin K-M, Schuetz C, Jacobsen E-M, Schulz AS, Schwarz K, Fischer A, Friedrich W, Cavazzana M. Reticular dysgenesis: International survey on clinical presentation, transplantation, and outcome. Blood 2017, 129(21), 2928-2938.
  • Heimall J, Buckley RH, Puck J, Fleisher TA, Gennery AR, Haddad E, Neven B, Slatter M, Skinner R, Baker KS, Dietz AC, Duncan C, Griffith LM, Notarangelo L, Pulsipher MA, Cowan MJ. Recommendations for Screening and Management of Late Effects in Patients with Severe Combined Immunodeficiency after Allogenic Hematopoietic Cell Transplantation: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric HCT. Biology of Blood and Marrow Transplantation 2017, 23(8), 1229-1240.
  • Schiroli G, Ferrari S, Conway A, Jacob A, Capo V, Albano L, Plati T, Castiello MC, Sanvito F, Gennery AR, Bovolenta C, Palchaudhuri R, Scadden DT, Holmes MC, Villa A, Sitia G, Lombardo A, Genovese P, Naldini L. Preclinical modeling highlights the therapeutic potential of hematopoietic stem cell gene editing for correction of SCID-X1. Science Translational Medicine 2017, 9(411), eaan0820.
  • Dobbs K, Tabellini G, Calzoni E, Patrizi O, Martinez P, Giliani SC, Moratto D, Al-Herz W, Cancrini C, Cowan M, Bleesing J, Booth C, Buchbinder D, Burns SO, Chatila TA, Chou J, Daza-Cajigal V, de Bruin LMO, de la Morena M, Di Matteo G, Finocchi A, Geha R, Goyal RK, Hayward A, Holland S, Huang C-H, Kanariou MG, King A, Kaplan B, Kleva A, Kuijpers TW, Lee BW, Lougaris V, Massaad M, Meyts I, Morsheimer M, Neven B, Pai S-Y, Plebani A, Prockop S, Reisli I, Soh JY, Somech R, Torgerson TR, Kim Y-J, Walter JE, Gennery AR, Keles S, Manis JP, Marcenaro E, Moretta A, Parolini S, Notarangelo LD. Natural killer cells from patients with recombinase-activating gene and non-homologous end joining gene defects comprise a higher frequency of CD56^bright NKG2A⁺⁺⁺ cells, and yet display increased degranulation and higher perforin content. Frontiers in Immunology 2017, 8, 798.
  • Yeates L, Slatter MA, Gennery AR. Infusion of sibling marrow in a patient with Purine nucleoside phosphorylase deficiency leads to split mixed donor chimerism and normal immunity. Frontiers in Pediatrics 2017, 5, 143.
  • Battersby AC, Braggins H, Pearce MS, Cale CM, Burns SO, Hackett S, Hughes S, Barge D, Goldblatt D, Gennery AR. Inflammatory and autoimmune manifestations in X-linked carriers of chronic granulomatous disease in the United Kingdom. Journal of Allergy and Clinical Immunology 2017, 140(2), 628-630.e6.
  • Engelhardt KR, Xu Y, Grainger A, Germani Batacchi MGC, Swan DJ, Willet JDP, Abd Hamid IJ, Agyeman P, Barge D, Bibi S, Jenkins L, Flood TJ, Abinun M, Slatter MA, Gennery AR, Cant AJ, Santibanez Koref M, Gilmour K, Hambleton S. Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing. Journal of Clinical Immunology 2017, 37(1), 42-50.
  • Miot C, Imai K, Imai C, Mancini AJ, Kucuk ZY, Kawai T, Nishikomori R, Ito E, Pellier I, Girod SD, Rosain J, Sasaki S, Chandrakasan S, Schmid JP, Okano T, Colin E, Olaya-Vargas A, Yamazaki-Nakashimada M, Qasim W, Padilla SE, Jones A, Krol A, Cole N, Jolles S, Bleesing J, Vraetz T, Gennery AR, Abinun M, Gungor T, Costa-Carvalho B, Condino-Neto A, Veys P, Holland SM, Uzel G, Moshous D, Neven B, Blanche S, Ehl S, Doffinger R, Patel SY, Puel A, Bustamante J, Gelfand EW, Casanova J-L, Orange JS, Picard C. Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations. Blood 2017, 130(12), 1456-1467.
  • Heimall J, Puck J, Buckley R, Fleisher TA, Gennery AR, Neven B, Slatter M, Haddad E, Notarangelo LD, Baker KS, Dietz AC, Duncan C, Pulsipher MA, Cowan MJ. Current Knowledge and Priorities for Future Research in Late Effects after Hematopoietic Stem Cell Transplantation (HCT) for Severe Combined Immunodeficiency Patients: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric HCT. Biology of Blood and Marrow Transplantation 2017, 23(3), 379-387.
  • Shekhovtsova Z, Bonfim C, Ruggeri A, Nichele S, Page K, Alseraihy A, Barriga F, de Toledo Codina JS, Veys P, Boelens JJ, Mellgren K, Bittencourt H, O'Brien T, Shaw PJ, Chybicka A, Volt F, Giannotti F, Gluckman E, Kurtzberg J, Gennery AR, Rocha V. A risk factor analysis of outcomes after unrelated cord blood transplantation for children with Wiskott-Aldrich syndrome. Haematologica 2017, 102(6), 1112-1119.
  • Morillo-Gutierrez B, Beier R, Rao K, Burroughs L, Schulz A, Ewins AM, Gibson B, Sedlacek P, Krol L, Strahm B, Zaidman I, Kalwak K, Talano JA, Woolfrey A, Fraser C, Meyts I, Muller I, Wachowiak J, Bernardo ME, Veys P, Sykora KW, Gennery AR, Slatter M. Treosulfan-based conditioning for allogeneic HSCT in children with chronic granulomatous disease: a multicenter experience. Blood 2016, 128(3), 440-448.
  • Bryan BA, Battersby A, Shillitoe BMJ, Barge D, Bourne H, Flood T, Cant AJ, Stroud C, Gennery AR. Respiratory Health and Related Quality of Life in Patients with Congenital Agammaglobulinemia in the Northern Region of the UK. Journal of Clinical Immunology 2016, 36(5), 472-479.
  • Beattie B, Cole D, Nicholson L, Leech S, Taylor A, Robson H, Guest J, Wang XN, Gennery AR. Limited thymic recovery after extracorporeal photopheresis in a low-body-weight patient with acute graft-versus-host disease of the skin. Journal of Allergy and Clinical Immunology 2016, 137(6), 1890-1893.
  • Nademi Z, Slatter MA, Dvorak CC, Neven B, Fischer A, Suarez F, Booth C, Rao K, Laberko A, Rodina J, Bertrand Y, Koltan S, Debski R, Flood T, Abinun M, Gennery AR, Hambleton S, Ehl S, Cant AJ. Hematopoietic stem cell transplant in patients with activated PI3K delta syndrome. Journal of Allergy and Clinical Immunology 2016, 139(6), 1046-1049.
  • Naik S, Nicholas SK, Martinez CA, Leen AM, Hanley PJ, Gottschalk SM, Rooney CM, Hanson IC, Krance RA, Shpall EJ, Cruz CR, Amrolia P, Lucchini G, Bunin N, Heimall J, Klein OR, Gennery AR, Slatter MA, Vickers MA, Orange JS, Heslop HE, Bollard CM, Keller MD. Adoptive immunotherapy for primary immunodeficiency disorders with virus-specific T lymphocytes. Journal of Allergy and Clinical Immunology 2016, 137(5), 1498-1505.e1.
  • Guo CW, Nakazawa Y, Woodbine L, Bjorkman A, Shimada M, Fawcett H, Jia N, Ohyama K, Li TS, Nagayama Y, Mitsutake N, Pan-Hammarstrom Q, Gennery AR, Lehmann AR, Jeggo PA, Ogi T. XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency. Journal of Allergy and Clinical Immunology 2015, 136(4), 1007-1017.
  • Ip W, Gaspar HB, Kleta R, Chanudet E, Bacchelli C, Pitts A, Nademi Z, Davies EG, Slatter MA, Amrolia P, Rao K, Veys P, Gennery AR, Qasim W. Variable Phenotype of Severe Immunodeficiencies Associated with RMRP Gene Mutations. Journal of Clinical Immunology 2015, 35(2), 147-157.
  • Slatter MA, Boztug H, Potschger U, Sykora KW, Lankester A, Yaniv I, Sedlacek P, Glogova E, Veys P, Gennery AR, Peters C, EBMT Inborn Errors Paediat Dis Wor. Treosulfan-based conditioning regimens for allogeneic haematopoietic stem cell transplantation in children with non-malignant diseases. Bone Marrow Transplantation 2015, 50(12), 1536-1541.
  • Engelhardt KR, Gertz ME, Keles S, Schaffer AA, Sigmund EC, Glocker C, Saghafi S, Pourpak Z, Ceja R, Sassi A, Graham LE, Massaad MJ, Mellouli F, Ben-Mustapha I, Khemiri M, Kilic SS, Etzioni A, Freeman AF, Thiel J, Schulze I, Al-Herz W, Metin A, Sanal O, Tezcan I, Yeganeh M, Niehues T, Dueckers G, Weinspach S, Patiroglu T, Unal E, Dasouki M, Yilmaz M, Genel F, Aytekin C, Kutukculer N, Somer A, Kilic M, Reisli I, Camcioglu Y, Gennery AR, Cant AJ, Jones A, Gaspar BH, Arkwright PD, Pietrogrande MC, Baz Z, Al-Tamemi S, Lougaris V, Lefranc G, Megarbane A, Boutros J, Galal N, Bejaoui M, Barbouche MR, Geha RS, Chatila TA, Grimbacher B. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency. Journal of Allergy and Clinical Immunology 2015, 136(2), 402-412.
  • Elemraid MA, Thomas MF, Blain AP, Rushton SP, Spencer DA, Gennery AR, Clark JE, North East England Pediat Resp. Risk Factors for the Development of Pleural Empyema in Children. Pediatric Pulmonology 2015, 50(7), 721-726.
  • Wolska-Kusnierz B, Gregorek H, Chrzanowska K, Piatosa B, Pietrucha B, Heropolitanska-Pliszka E, Pac M, Klaudel-Dreszler M, Kostyuchenko L, Pasic S, Marodi L, Belohradsky BH, Ciznar P, Shcherbina A, Kilic SS, Baumann U, Seidel MG, Gennery AR, Syczewska M, Mikoluc B, Kalwak K, Styczynski J, Pieczonka A, Drabko K, Wakulinska A, Gathmann B, Albert MH, Skarzynska U, Bernatowska E, Inborn Errors Working Party Soc. Nijmegen Breakage Syndrome: Clinical and Immunological Features, Long-Term Outcome and Treatment Options - a Retrospective Analysis. Journal of Clinical Immunology 2015, 35(6), 538-549.
  • Thijssen PE, Ito Y, Grillo G, Wang J, Velasco G, Nitta H, Unoki M, Yoshihara M, Suyama M, Sun Y, Lemmers RJLF, de Greef JC, Gennery A, Picco P, Kloeckener-Gruissem B, Gungor T, Reisli I, Picard C, Kebaili K, Roquelaure B, Iwai T, Kondo I, Kubota T, van Ostaijen-Ten Dam MM, van Tol MJD, Weemaes C, Francastel C, van der Maarel SM, Sasaki H. Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome. Nature Communications 2015, 6, 7870.
  • Wehr C, Gennery AR, Lindemans C, Schulz A, Hoenig M, Marks R, Recher M, Gruhn B, Holbro A, Heijnen I, Meyer D, Grigoleit G, Einsele H, Baumann U, Witte T, Sykora K-W, Goldacker S, Regairaz L, Aksoylar S, Ardeniz O, Zecca M, Zdziarski P, Meyts I, Matthes-Martin S, Imai K, Kamae C, Fielding A, Seneviratne S, Mahlaoui N, Slatter MA, Gungor T, Arkwright PD, Van Montfrans J, Sullivan KE, Grimbacher B, Cant A, Peter H-H, Finke J, Gaspar HB, Warnatz K, Rizzi M. Multicenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency. Journal of Allergy and Clinical Immunology 2015, 135(4), 988-997.e6.
  • Zheng J, vandeVeerdonk FL, Crossland KL, Smeekens SP, Chan CM, AlShehri T, Abinun M, Gennery AR, Mann J, Lendrem DW, Netea MG, Rowan AD, Lilic D. Gain-of-function STAT1 mutations impair STAT3 activity in patients with Chronic Mucocutaneous Candidiasis (CMC). European Journal of Immunology 2015, 45(10), 2834-2846.
  • Irving CA, Carter V, Gennery AR, Parry G, Griselli M, Hasan A, Kirk CR. Effect of persistent versus transient donor-specific HLA antibodies on graft outcomes in pediatric cardiac transplantation. Journal of Heart and Lung Transplantation 2015, 34(10), 1310-1317.
  • Aydin SE, Kilic SS, Aytekin C, Kumar A, Porras O, Kainulainen L, Kostyuchenko L, Genel F, Kutukculer N, Karaca N, Gonzalez-Granado L, Abbott J, Al-Zahrani D, Rezaei N, Baz Z, Thiel J, Ehl S, Marodi L, Orange JS, Sawalle-Belohradsky J, Keles S, Holland SM, Sanal O, Ayvaz DC, Tezcan I, Al-Mousa H, Alsum Z, Hawwari A, Metin A, Matthes-Martin S, Honig M, Schulz A, Picard C, Barlogis V, Gennery A, Ifversen M, van Montfrans J, Kuijpers T, Bredius R, Duckers G, Al-Herz W, Pai S-Y, Geha R, Notheis G, Schwarze C-P, Tavil B, Azik F, Bienemann K, Grimbacher B, Heinz V, Gaspar HB, Aydin R, Hagl B, Gathmann B, Belohradsky BH, Ochs HD, Chatila T, Renner ED, Su H, Freeman AF, Engelhardt K, Albert MH. DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients. Journal of Clinical Immunology 2015, 35(2), 189-198.
  • Walter JE, Rosen LB, Csomos K, Rosenberg JM, Mathew D, Keszei M, Ujhazi B, Chen K, Lee YN, Tirosh I, Dobbs K, Al-Herz W, Cowan MJ, Puck J, Bleesing JJ, Grimley MS, Malech H, De Ravin SS, Gennery AR, Abraham RS, Joshi AY, Boyce TG, Butte MJ, Nadeau KC, Balboni I, Sullivan KE, Akhter J, Adeli M, El-Feky RA, El-Ghoneimy DH, Dbaibo G, Wakim R, Azzari C, Palma P, Cancrini C, Capuder K, Condino-Neto A, Costa-Carvalho BT, Oliveira JB, Roifman C, Buchbinder D, Kumanovics A, Franco JL, Niehues T, Schuetz C, Kuijpers T, Yee C, Chou J, Masaad MJ, Geha R, Uze G, Gelman R, Holland SM, Recher M, Utz PJ, Browne SK, Notarangelo LD. Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency. Journal of Clinical Investigation 2015, 125(11), 4135-4148.
  • Irving CA, Gennery AR, Carter V, Wallis JP, Hasan A, Griselli M, Kirk R. ABO-incompatible cardiac transplantation in pediatric patients with high isohemagglutinin titers. Journal of Heart and Lung Transplantation 2015, 34(8), 1095-1102.
  • Speckmann C, Doerken S, Aiuti A, Albert MH, Al-Herz W, Allende LM, Scarselli A, Avcin T, Perez-Becker R, Cancrini C, Cant A, Di Cesare S, Finocchi A, Fischer A, Gaspar HB, Ghosh S, Gennery A, Gilmour K, Gonzalez-Granado LI, Martinez-Gallo M, Hambleton S, Hauck F, Hoenig M, Moshous D, Neven B, Niehues T, Notarangelo L, Picard C, Rieber N, Schulz A, Schwarz K, Seidel MG, Soler-Palacin P, Stepensky P, Strahm B, Vraetz T, Warnatz K, Winterhalter C, Worth A, Fuchs S, Uhlmann A, Ehl S. A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis. Journal of Allergy and Clinical Immunology 2015, 139(4), 1302-1310.e4.
  • Elemraid MA, Rushton SP, Thomas MF, Spencer DA, Gennery AR, Clark JE. Utility of inflammatory markers in predicting the aetiology of pneumonia in children. Diagnostic Microbiology and Infectious Disease 2014, 79(4), 458-462.
  • Habel A, Herriot R, Kumararatne D, Allgrove J, Baker K, Baxendale H, Bu'Lock F, Firth H, Gennery A, Holland A, Illingworth C, Mercer N, Pannebakker M, Parry A, Roberts A, Tsai-Goodman B. Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times. European Journal of Pediatrics 2014, 173(6), 757-765.
  • Edgar JDM, Buckland M, Guzman D, Conlon NP, Knerr V, Bangs C, Reiser V, Panahloo Z, Workman S, Slatter M, Gennery AR, Davies EG, Allwood Z, Arkwright PD, Helbert M, Longhurst HJ, Grigoriadou S, Devlin LA, Huissoon A, Krishna MT, Hackett S, Kumararatne DS, Condliffe AM, Baxendale H, Henderson K, Bethune C, Symons C, Wood P, Ford K, Patel S, Jain R, Jolles S, El-Shanawany T, Alachkar H, Herwadkar A, Sargur R, Shrimpton A, Hayman G, Abuzakouk M, Spickett G, Darroch CJ, Paulus S, Marshall SE, McDermott EM, Heath PT, Herriot R, Noorani S, Turner M, Khan S, Grimbacher B. The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years' activity 2008-2012. Clinical and Experimental Immunology 2014, 175(1), 68-78.
  • Dickinson RE, Milne P, Jardine L, Zandi S, Swierczek SI, McGovern N, Cookson S, Ferozepurwalla Z, Langridge A, Pagan S, Gennery A, Heiskanen-Kosma T, Hamalainen S, Seppanen M, Helbert M, Tholouli E, Gambineri E, Reykdal S, Gottfreosson M, Thaventhiran JE, Morris E, Hirschfield G, Richter AG, Jolles S, Bacon CM, Hambleton S, Haniffa M, Bryceson Y, Allen C, Prchal JT, Dick JE, Bigley V, Collin M. The evolution of cellular deficiency in GATA2 mutation. Blood 2014, 123(6), 863-874.
  • Woodbine L, Gennery AR, Jeggo PA. The clinical impact of deficiency in DNA non-homologous end-joining. DNA Repair 2014, 16, 84-96.
  • Woodbine L, Gennery AR, Jeggo PA. Reprint of "The clinical impact of deficiency in DNA non-homologous end-joining". DNA Repair 2014, 17, 9-20.
  • Gungor T, Teira P, Slatter M, Stussi G, Stepensky P, Moshous D, Vermont C, Ahmad I, Shaw PJ, da Cunha JMT, Schlegel PG, Hough R, Fasth A, Kentouche K, Gruhn B, Fernandes JF, Lachance S, Bredius R, Resnick IB, Belohradsky BH, Gennery A, Fischer A, Gaspar HB, Schanz U, Seger R, Rentsch K, Veys P, Haddad E, Albert MH, Hassan M, Inborn Errors Working Party Europe. Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study. Lancet 2014, 383(9915), 436-448.
  • Elemraid M, Pollard K, Thomas M, Simmister C, Spencer D, Rushton S, Gennery A, Clark J. Parental decisions on children participating in research: Mohamed Elemraid and colleagues consider what influences parents in allowing their child to be enrolled in clinical research. Nursing Children and Young People 2014, 25(8), 16-21.
  • Lane JR, Evans PTG, Nademi Z, Barge D, Jackson A, Hambleton S, Flood TJ, Cant AJ, Abinun M, Slatter MA, Gennery AR. Low-Dose Serotherapy Improves Early Immune Reconstitution after Cord Blood Transplantation for Primary Immunodeficiencies. Biology of Blood and Marrow Transplantation 2014, 20(2), 243-249.
  • Qasim W, Gennery AR. Gene Therapy for Primary Immunodeficiencies: Current Status and Future Prospects. Drugs 2014, 74(9), 963-969.
  • la Marca G, Canessa C, Giocaliere E, Romano F, Malvagia S, Funghini S, Moriondo M, Valleriani C, Lippi F, Ombrone D, Della Bona ML, Speckmann C, Borte S, Brodszki N, Gennery AR, Weinacht K, Celmeli F, Pagel J, de Martino M, Guerrini R, Wittkowski H, Santisteban I, Bali P, Ikinciogullari A, Hershfield M, Notarangelo LD, Resti M, Azzari C. Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots. Journal of Allergy and Clinical Immunology 2014, 134(1), 155-159.e.
  • Dvorak CC, Hassan A, Slatter MA, Honig M, Lankester AC, Buckley RH, Pulsipher MA, Davis JH, Gungor T, Gabriel M, Bleesing JH, Bunin N, Sedlacek P, Connell JA, Crawford DF, Notarangelo LD, Pai SY, Hassid J, Veys P, Gennery AR, Cowan MJ. Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency. Journal of Allergy and Clinical Immunology 2014, 134(4), 935-943.e15.
  • Elemraid MA, Rushton SP, Thomas MF, Spencer DA, Eastham KM, Gennery AR, Clark JE, North East England Paediatric Respiratory Infection Study Group. Changing clinical practice: management of paediatric community-acquired pneumonia. Journal of Evaluation in Clinical Practice 2014, 20(1), 94-99.
  • Elemraid MA, Muller M, Spencer DA, Rushton SP, Gorton R, Thomas MF, Eastham KM, Hampton F, Gennery AR, Clark JE, North East England Paediat Resp In. Accuracy of the Interpretation of Chest Radiographs for the Diagnosis of Paediatric Pneumonia. PLoS One 2014, 9(8), e106051.
  • Lee YN, Frugoni F, Dobbs K, Walter JE, Giliani S, Gennery AR, Al-Herz W, Haddad E, LeDeist F, Bleesing JH, Lauren AH, Pai SY, Nelson RP, El-Ghoneimy DH, El-Feky RA, Reda SM, Hossny E, Soler-Palacin P, Fuleihan RL, Patel NC, Massaad MJ, Geha RS, Puck JM, Palma P, Cancrini C, Chen K, Vihinen M, Alt FW, Notarangelo LD. A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency. Journal of Allergy and Clinical Immunology 2014, 133(4), 1099-1108.e12.
  • Elemraid MA, Rushton SP, Clark JE, Perry JD, Thomas MF, Sails AD, Gennery AR, Spencer DA, North East of England Paediatric Respiratory Infection Study Group. A Case-Control Study to Assess the Urinary Pneumococcal Antigen Test in Childhood Pneumonia. Clinical Pediatrics 2014, 53(3), 286-288.
  • Elemraid MA, Sails AD, Thomas MF, Rushton SP, Perry JD, Eltringham GJA, Spencer DA, Eastham KM, Hampton F, Gennery AR, Clark JE, North East of England Paediatric Respiratory Infection Study Group. Pneumococcal diagnosis and serotypes in childhood community-acquired pneumonia. Diagnostic Microbiology and Infectious Disease 2013, 76(2), 129-132.
  • Elemraid M, Pollard K, Thomas M, Simmister C, Spencer D, Rushton S, Gennery A, Clark J. Parental decisions on children participating in research. Nursing Children and Young People 2013, 25(8), 16-21.
  • Harkensee C, Oka A, Onizuka M, Middleton PG, Inoko H, Nakaoka H, Gennery AR, Ando K, Morishima Y, Japan Marrow Donor Programme. Microsatellite scanning of the immunogenome associates MAPK14 and ELTD1 with graft-versus-host disease in hematopoietic stem cell transplantation. Immunogenetics 2013, 65(6), 417-427.
  • Elemraid MA, Rushton SP, Shirley MDF, Thomas MF, Spencer DA, Eastham KM, Hampton F, Gorton R, Pollard K, Gennery AR, Clark JE, North East of England Paediatric Respiratory Infection Study Group. Impact of the 7-valent pneumococcal conjugate vaccine on the incidence of childhood pneumonia. Epidemiology and Infection 2013, 141(8), 1697-1704.
  • Cole T, McKendrick F, Titman P, Cant AJ, Pearce MS, Cale CM, Goldblatt D, Gennery AR. Health Related Quality of Life and Emotional Health in Children with Chronic Granulomatous Disease: A Comparison of Those Managed Conservatively with Those That Have Undergone Haematopoietic Stem Cell Transplant. Journal of Clinical Immunology 2013, 33(1), 8-13.
  • Sinha A, Abinun M, Gennery AR, Barge D, Slatter M, Cheetham T. Graves' Immune Reconstitution Inflammatory Syndrome in Childhood. Thyroid 2013, 23(8), 1010-1014.
  • Cole TS, McKendrick F, Cant AJ, Pearce MS, Cale CM, Goldblatt DR, Gennery AR, Titman P. Cognitive Ability in Children with Chronic Granulomatous Disease: A Comparison of Those Managed Conservatively with Those Who Have Undergone Hematopoietic Stem Cell Transplant. Neuropediatrics 2013, 44(4), 230-232.
  • Cole T, Pearce MS, Cant AJ, Cale CM, Goldblatt D, Gennery AR. Clinical outcome in children with chronic granulomatous disease managed conservatively or with hematopoietic stem cell transplantation. Journal of Allergy and Clinical Immunology 2013, 132(5), 1150-1155.
  • Tilgner K, Neganova I, Singhapol C, Saretzki G, Al-Aama JY, Evans J, Gorbunova V, Gennery A, Przyborski S, Stojkovic M, Armstrong L, Jeggo P, Lako M. Brief Report: A Human Induced Pluripotent Stem Cell Model of Cernunnos Deficiency Reveals an Important Role for XLF in the Survival of the Primitive Hematopoietic Progenitors. Stem Cells 2013, 31(9), 2015-2023.
  • Elemraid MA, Sails AD, Eltringham GJA, Perry JD, Rushton SP, Spencer DA, Thomas MF, Eastham KM, Hampton F, Gennery AR, Clark JE, North East of England Paediatric Respiratory Infection Study Group. Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine. European Respiratory Journal 2013, 42(6), 1595-1603.
  • Tilgner K, Neganova I, Moreno-Gimeno I, Al-Aama JY, Burks D, Yung S, Singhapol C, Saretzki G, Evans J, Gorbunova V, Gennery A, Pryzborski S, Stojkovic M, Armstrong L, Jeggo P, Lako M. A human iPSC model of Ligase IV deficiency reveals an important role for NHEJ-mediated-DSB repair in the survival and genomic stability of induced pluripotent stem cells and emerging haematopoietic progenitors. Cell Death and Differentiation 2013, 20, 1089-1100.
  • Silva HM, Reis G, Guedes M, Cleto E, Vizcaino JR, Kelly D, Gennery AR, Silva ES. A case of hepatopulmonary syndrome solved by mycophenolate mofetil (an inhibitor of angiogenesis and nitric oxide production). Journal of Hepatology 2013, 58(3), 630-633.
  • Booth C, Gilmour KC, Veys P, Gennery AR, Slatter MA, Chapel H, Heath PT, Steward CG, Smith O, O'Meara A, Kerrigan H, Mahlaoui N, Cavazzana-Calvo M, Fischer A, Moshous D, Blanche S, Pachlopnick-Schmid J, Latour S, de Saint-Basile G, Albert M, Notheis G, Rieber N, Strahm B, Ritterbusch H, Lankester A, Hartwig NG, Meyts I, Plebani A, Soresina A, Finocchi A, Pignata C, Cirillo E, Bonanomi S, Peters C, Kalwak K, Pasic S, Sedlacek P, Jazbec J, Kanegane H, Nichols KE, Hanson IC, Kapoor N, Haddad E, Cowan M, Choo S, Smart J, Arkwright PD, Gaspar HB. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease. Blood 2012, 117(1), 53-62.
  • Harkensee C, Oka A, Onizuka M, Middleton PG, Inoko H, Hirayasu K, Kashiwase K, Yabe T, Nakaoka H, Gennery AR, Ando K, Morishima Y, Japan Marrow Donor Program. Single nucleotide polymorphisms and outcome risk in unrelated mismatched hematopoietic stem cell transplantation: an exploration study. Blood 2012, 119(26), 6365-6372.
  • Cole TS, Johnstone IC, Pearce MS, Fulton B, Cant AJ, Gennery AR, Slatter MA. Outcome of children requiring intensive care following haematopoietic SCT for primary immunodeficiency and other non-malignant disorders. Bone Marrow Transplantation 2012, 47(1), 40-45.
  • Du LK, Peng RJ, Bjorkman A, de Miranda NF, Rosner C, Kotnis A, Berglund M, Liu CH, Rosenquist R, Enblad G, Sundstrom C, Hojjat-Farsangi M, Rabbani H, Teixeira MR, Revy P, Durandy A, Zeng YX, Gennery AR, de Villartay JP, Pan-Hammarstrom Q. Cernunnos influences human immunoglobulin class switch recombination and may be associated with B cell lymphomagenesis. Journal of Experimental Medicine 2012, 209(2), 291-305.
  • Slatter MA, Rao K, Amrolia P, Flood T, Abinun M, Hambleton S, Nademi Z, Goulden N, Davies G, Qasim W, Gaspar HB, Cant A, Gennery AR, Veys P. Treosulfan-based conditioning regimens for hematopoietic stem cell transplantation in children with primary immunodeficiency: United Kingdom experience. Blood 2011, 117(16), 4367-4375.
  • Brown L, Xu-Bayford J, Allwood Z, Slatter M, Cant A, Davies EG, Veys P, Gennery AR, Gaspar HB. Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening. Blood 2011, 117(11), 3243-3246.
  • de Greef JC, Wang J, Balog J, den Dunnen JT, Frants RR, Straasheijm KR, Aytekin C, van der Burg M, Duprez L, Ferster A, Gennery AR, Gimelli G, Reisli I, Schuetz C, Schulz A, Smeets DFCM, Sznajer Y, Wijmenga C, van Eggermond MC, van Ostaijen-ten Dam MM, Lankester AC, van Tol MJD, van den Elsen PJ, Weemaes CM, van der Maarel SM. Mutations in Z8T824 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2. American Journal of Human Genetics 2011, 88(6), 796-804.
  • Pessach IM, Ordovas-Montanes J, Zhang SY, Casanova JL, Giliani S, Gennery AR, Al-Herz W, Manos PD, Schlaeger TM, Park IH, Rucci F, Agarwal S, Mostoslavsky G, Daley GQ, Notarangelo LD. Induced pluripotent stem cells: A novel frontier in the study of human primary immunodeficiencies. Journal of Allergy and Clinical Immunology 2011, 127(6), 1400-U140.
  • Recher M, Berglund LJ, Avery DT, Cowan MJ, Gennery AR, Smart J, Peake J, Wong M, Pai SY, Baxi S, Walter JE, Palendira U, Tangye GA, Rice M, Brothers S, Al-Herz W, Oettgen H, Eibel H, Puck JM, Cattaneo F, Ziegler JB, Giliani S, Tangye SG, Notarangelo LD. IL-21 is the primary common gamma chain-binding cytokine required for human B-cell differentiation in vivo. Blood 2011, 118(26), 6824-6835.
  • McLean-Tooke A, Barge D, Spickett GP, Gennery AR. Flow Cytometric Analysis of TCR V beta Repertoire in Patients with 22q11.2 Deletion Syndrome. Scandinavian Journal of Immunology 2011, 73(6), 577-585.
  • Subbarayan A, Colarusso G, Hughes SM, Gennery AR, Slatter M, Cant AJ, Arkwright PD. Clinical Features That Identify Children With Primary Immunodeficiency Diseases. Pediatrics 2011, 127(5), 810-816.
  • Smeekens SP, Plantinga TS, van de Veerdonk FL, Heinhuis B, Hoischen A, Joosten LAB, Arkwright PD, Gennery A, Kullberg BJ, Veltman JA, Lilic D, van der Meer JWM, Netea MG. STAT1 hyperphosphorylation and defective IL12R/IL23R signaling underlie defective immunity in autosomal dominant Chronic Mucocutaneous Candidiasis. PLoS One 2011, 6(12), e29248.
  • Gennery AR, Slatter MA, Grandin L, Taupin P, Cant AJ, Veys P, Amrolia PJ, Gaspar HB, Davies EG, Friedrich W, Hoenig M, Notarangelo LD, Mazzolari E, Porta F, Bredius RGM, Lankester AC, Wulffraat NM, Seger R, Gungor T, Fasth A, Sedlacek P, Neven B, Blanche S, Fischer A, Cavazzana-Calvo M, Landais P, and Members of the Inborn Errors Working Party. Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: Entering a new century, do we do better?. Journal of Allergy and Clinical Immunology 2010, 126(3), 602-610.
  • Albert MH, Gennery AR, Greil J, Cale CM, Kalwak K, Kondratenko I, Mlynarski W, Notheis G, Fuhrer M, Schmid I, Belohradsky BH. Successful SCT for Nijmegen breakage syndrome. Bone Marrow Transplantation 2010, 45(4), 622-626.
  • Moss SJ, Fenton AC, Toomey JA, Grainger AJ, Smith J, Gennery AR. Responses to a Conjugate Pneumococcal Vaccine in Preterm Infants Immunized at 2, 3, and 4 Months of Age. Clinical and Vaccine Immunology 2010, 17(11), 1810-1816.
  • Woellner C, Gertz EM, Schaffer AA, Lagos M, Perro M, Glocker EO, Pietrogrande MC, Cossu F, Franco JL, Matamoros N, Pietrucha B, Heropolitanska-Pliszka E, Yeganeh M, Moin M, Espanol T, Ehl S, Gennery AR, Abinun M, Breborowicz A, Niehues T, Kilic SS, Junker A, Turvey SE, Plebani A, Sanchez B, Garty BZ, Pignata C, Cancrini C, Litzman J, Sanal O, Baumann U, Bacchetta R, Hsu AP, Davis JN, Hammarstrom L, Davies EG, Eren E, Arkwright PD, Moilanen JS, Viemann D, Khan S, Laszlo M, Cant AJ, Freeman AF, Puck JM, Holland SM, Grimbacher B. Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome. Journal of Allergy and Clinical Immunology 2010, 125(2), 424-432.
  • Laugel V, Dalloz C, Durand M, Sauvanaud F, Kristensen U, Vincent MC, Pasquier L, Odent S, Cormier-Daire V, Gener B, Tobias ES, Tolmie JL, Martin-Coignard D, Drouin-Garraud V, Heron D, Journel H, Raffo E, Vigneron J, Lyonnet S, Murday V, Gubser-Mercati D, Funalot B, Brueton L, del Pozo JS, Munoz E, Gennery AR, Salih M, Noruzinia M, Prescott K, Ramos L, Stark Z, Fieggen K, Chabrol B, Sarda P, Edery P, Bloch-Zupan A, Fawcett H, Pham D, Egly JM, Lehmann AR, Sarasin A, Dollfus H. Mutation Update for the CSB/ERCC6 and CSA/ERCC8 Genes Involved in Cockayne Syndrome. Human Mutation 2010, 31(2), 113-126.
  • Janda A, Sedlacek P, Honig M, Friedrich W, Champagne M, Matsumoto T, Fischer A, Neven B, Contet A, Bensoussan D, Bordigoni P, Loeb D, Savage W, Jabado N, Bonilla FA, Slatter MA, Davies EG, Gennery AR. Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly. Blood 2010, 116(13), 2229-2236.
  • Moss SJ, Fenton AC, Toomey J, Grainger A, Borrow R, Balmer P, Smith J, Gennery AR. Immunogenicity of a Heptavalent Conjugate Pneumococcal Vaccine Administered Concurrently with a Combination Diphtheria, Tetanus, Five-Component Acellular Pertussis, Inactivated Polio, and Haemophilus influenzae Type b Vaccine and a Meningococcal Group C Conjugate Vaccine at 2, 3, and 4 Months of Age. Clinical and Vaccine Immunology 2010, 17(3), 311-316.
  • Walter JE, Rucci F, Patrizi L, Recher M, Regenass S, Paganini T, Keszei M, Pessach I, Lang PA, Poliani PL, Giliani S, Al-Herz W, Cowan MJ, Puck JM, Bleesing J, Niehues T, Schuetz C, Malech H, DeRavin SS, Facchetti F, Gennery AR, Andersson E, Kamani NR, Sekiguchi J, Alenezi HM, Chinen J, Dbaibo G, ElGhazali G, Fontana A, Pasic S, Detre C, Terhorst C, Alt FW, Notarangelo LD. Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency. Journal of Experimental Medicine 2010, 207(7), 1541-1554.
  • Bordon V, Gennery AR, Slatter MA, Vandecruys E, Laureys G, Veys P, Waseem Q, Friedrich W, Wulfraat NM, Scherer F, Cant AJ, Fischer A, Cavazanna-Calvo M, Bredius RGM, Notarangelo LD, Mazzolari E, Neven B, Tayfun G. Clinical and immunologic outcome of patients with cartilage hair hypoplasia after hematopoietic stem cell transplantation. Blood 2010, 116(1), 27-35.
  • Herwadkar A, Gennery AR, Moran AS, Haeney MR, Arkwright PD. Association between hypoparathyroidism and defective T cell immunity in 22q11.2 deletion syndrome. Journal of Clinical Pathology 2010, 63(2), 151-155.
  • Qasim W, Cavazzana-Calvo M, Davies G, Davis J, Duval M, Eames G, Farhina N, Filipovich A, Fischer A, Friedrich W, Gennery A, Heilmann C, Landais P, Horwitz M, Porto F, Sedlacek P, Seger R, Slatter M, Teague L, Eapen M, Veys P. Worldwide experience of allogeneic stem cell transplantation for Leukocyte Adhesion Deficiency at 1993-2007. Pediatrics 2009, 123, 836-40.
  • Soncini E, Slatter MA, Jones LBKR, Hughes S, Hodges S, Flood TJ, Barge D, Spickett GP, Jackson GH, Collin MP, Abinun M, Cant AJ, Gennery AR. Unrelated donor and HLA-identical sibling haematopoietic stem cell transplantation cure chronic granulomatous disease with good long-term outcome and growth. British Journal of Haematology 2009, 145(1), 73-83.
  • Shaw BE, Veys P, Pagliuca A, Addada J, Cook G, Craddock CF, Gennery AR, Goldman J, Mackinnon S, Madrigal JA, Marks DI, Navarrete C, Potter MN, Querol S, Regan F, Russell NH, Hough RE. Recommendations for a standard UK approach to incorporating umbilical cord blood into clinical transplantation practice: conditioning protocols and donor selection algorithms. Bone Marrow Transplantation 2009, 44(1), 7-12.
  • Hong M, Ryan KR, Arkwright P, Gennery A, Costigan C, Denning D, Cant AJ, Abinun M, Young DA, McConnell V, Spickett GP, Swan DC, Gillespie CS, Lilac D, Dominguez M. Pattern recognition receptor expression is not impaired in patients with chronic mucocutanous candidiasis with or without autoimmune polyendocrinopathy candidiasis ectodermal dystrophy. Clinical and Experimental Immunology 2009, 156(1), 40-51.
  • Cote M, Menager MM, Burgess A, Mahlaoui N, Picard C, Schaffner C, Al-Manjomi F, Al-Harbi M, Alangari A, Le Deist F, Gennery AR, Prince N, Cariou A, Nitschke P, Blank U, El-Ghazali G, Menasche G, Latour S, Fischer A, de Saint Basile G. Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells. Journal of Clinical Investigation 2009, 119(12), 3765-3773.
  • Engelhardt K, McGhee S, Winkler S, Sassi A, Woellner C, Lopez-Herrera G, Chen A, Kim H, Lloret M, Schulze I, Ehl S, Thiel J, Pfeifer D, Veelken H, Niehues T, Siepermann K, Weinspach S, Reisli I, Keles S, Genel F, Kutuculer N, Camcioǧlu Y, Somer A, Karakoc-Aydiner E, Barlan I, Gennery A, Metin A, Degerliyurt A, Pietrogrande M, Yeganeh M, Baz Z, Al-Tamemi S, Klein C, Puck J, Holland S, McCabe E, Grimbacher B, Chatila T. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome. Journal of Allergy and Clinical Immunology 2009, 124(6), 1289-1302.e4.
  • Straathof KC, Rao K, Eyrich M, Hale G, Bird P, Berrie E, Brown L, Adams S, Schlegel PG, Goulden N, Gaspar HB, Gennery AR, Landais P, Davies EG, Brenner MK, Veys PA, Amrolia PJ. Haemopoietic stem cell transplantation with antibody-based minimal intensity conditioning: a phase 1/2 study. Lancet 2009, 374(9693), 912-920.
  • Poliani PL, Facchetti F, Ravanini M, Gennery AR, Villa A, Roifman CM, Notarangelo LD. Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: possible implications for the pathophysiology of Omenn syndrome. Blood 2009, 114(1), 105-108.
  • Qasim W, Cavazzana-Calvo M, Davies EG, Davis J, Duval M, Eames G, Farinha N, Filopovich A, Fischer A, Friedrich W, Gennery A, Heilmann C, Landais P, Horwitz M, Porta F, Sedlacek P, Seger R, Slatten M, Teague L, Eapen M, Veys P. Allogeneic Hematopoietic Stem-Cell Transplantation for Leukocyte Adhesion Deficiency. Pediatrics 2009, 123(3), 836-840.
  • McLean-Tooke A, Barge D, Spickett GP, Gennery AR. T cell receptor Vb repertoire of T Lymphocytes and T regulatory cells by Flow cytometric Analysis in healthy children. Clinical and Experimental Immunology 2008, 151(1), 190-198.
  • Jones LBKR, McGrogan P, Flood TJ, Gennery AR, Morton L, Thrasher A, Goldblatt D, Parker L, Cant AJ. Special Article: Chronic granulomatous disease in the United Kingdom and Ireland: A comprehensive national patient-based registry. Clinical and Experimental Immunology 2008, 152(2), 211-218.
  • Harkensee C, Vasdev N, Gennery AR, Willetts IE, Taylor C. Prevention and management of BK-virus associated haemorrhagic cystitis in children following haematopoietic stem cell transplantation – a systematic review and evidence-based guidance for clinical management. British Journal of Haematology 2008, 142(5), 717-731.
  • Gennery AR, Slatter MA, Rice J, Hoefsloot LH, Barge D, McLean-Tooke A, Montgomery T, Goodship JA, Burt AD, Flood TJ, Abinun M, Cant AJ, Johnson D. Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome. Clinical and Experimental Immunology 2008, 153(1), 75-80.
  • Slatter MA, Brigham K, Dickinson AM, Harvey HL, Barge D, Jackson A, Bown N, Flood TJ, Cant AJ, Abinun M, Gennery AR. Long-term immune reconstitution after anti-CD52-treated or anti-CD34-treated hematopoietic stem cell transplantation for severe T-lymphocyte immunodeficiency. Journal of Allergy and Clinical Immunology 2008, 121(2), 361-367.
  • Du L, van der Burg M, Popov SW, Kotnis A, van Dongen JJM, Gennery AR, Pan-Hammarström Q. Involvement of Artemis in nonhomologous end-joining during immunoglobulin class switch recombination. Journal of Experimental Medicine 2008, 205(13), 3031-3040.
  • Ryan KR, Hong M, Arkwright PD, Gennery AR, Costigan C, Dominguez M, Denning D, McConnell V, Cant AJ, Abinun M, Spickett GP, Lilic D. Impaired dendritic cell maturation and cytokine production in patients with chronic mucocutanous candidiasis with or without APECED. Clinical and Experimental Immunology 2008, 154(3), 406-414.
  • McLean-Tooke A, Barge D, Spickett GP, Gennery AR. Immunological defects in 22q11.2 deletion syndrome. Journal of Allergy and Clinical Immunology 2008, 122(2), 362-367.
  • McLean-Tooke A, Barge D, Spickett GP, Gennery AR. Immunologic defects in 22q11.2 deletion syndrome. Journal of Allergy and Clinical Immunology 2008, 122(2), 362-367.
  • Gallimore CI, Taylor C, Gennery AR, Cant AJ, Galloway A, Xerry J, Adigwe J, Gray JJ. Contamination of the Hospital Environment with Gastroenteric Viruses: Comparison of Two Paediatric Wards over a Winter Season. Journal of Clinical Microbiology 2008, 46(9), 3112.
  • Hagleitner MM, Lankester A, Maraschio P, Hulten M, Frijns JP, Schütz C, Gimelli G, Davies EG, Gennery A, Belohradsky BH, de Groot R, Gerritsen EJA, Mattina T, Howard PJ, Fasth A, Reisli I, Furthner D, Slatter MA, Cant AJ, Cazzola G, van Dijken PJ, van Deuren IM, de Greef JC, van der Maarel SM, Weemaes CMR. Clinical spectrum of Immunodeficiency, Centromeric instability and Facial dysmorphism (ICF-syndrome). Journal of Medical Genetics 2008, 45(2), 93-99.
  • Meloni A, Furcas M, Cetani F, Marcocci C, Falorni A, Perniola R, Pura M, Wolff ASB, Husebye ES, Lilic D, Ryan KR, Gennery AR, Cant AJ, Abinun M, Spickett GP, Arkwright PD, Denning D, Costigan C, Dominguez M, McConnell V, Willcox N, Meager A. Autoantibodies against Type I Interferons as an Additional Diagnostic Criterion for Autoimmune Polyendocrine Syndrome Type I. Journal of Clinical Endocrinology & Metabolism 2008, 93(11), 4389-4397.
  • Gennery AR, Cant AJ. Advances in Hematopoietic Stem Cell Transplantation for Primary Immunodeficiency. Immunology and Allergy Clinics of North America 2008, 28(2), 439-456.
  • Du L, Dunn-Walters DK, Chrzanowska KH, Stankovic T, Kotnis A, Li X, Lu J, Brittain C, Popov SW, Gennery AR, Taylor AMR, Pan-Hammarström Q. A regulatory role for NBS1 in strand-specific mutagenesis during somatic hypermutation. PLoS ONE 2008, 3(6), e2482 (1-11).
  • Slatter MA, Rogerson EJ, Taylor CE, Galloway A, Clark JE, Flood TJ, Abinun M, Cant AJ, Gennery AR. Value of bronchoalveolar lavage before haematopoietic stem cell transplantation for primary immunodeficiency or autoimmune diseases. Bone Marrow Transplantation 2007, 40(6), 529-533.
  • Routledge DM, Jackson A, Bourn D, Bown NP, Cole M, Slatter MA, Gennery AR, Curtis A. Quantitative assessment of mixed chimerism in allogeneic stem cell transplant patients - A comparison of molecular genetic and cytogenetic approaches. Journal of Pediatric Hematology / Oncology 2007, 29(6), 428-431.
  • Larmouth W, Galloway A, Taylor C, Slatter M, Gennery A. Protective isolation - an argument in favour. Bone Marrow Transplantation 2007, 39, S250-S251.
  • Waruiru C, Slatter MA, Taylor C, Ramesh V, Flood TJ, Abinun M, Cant AJ, Gennery AR. Outcome of hematopoietic stem cell transplantation in severe combined immune deficiency with central nervous system viral infection. Pediatric Infectious Disease Journal 2007, 26(2), 129-133.
  • Gennery AR, Slatter MA, Rice JM, Hoefsloot LH, Barge D, McLean-Tooke A, Goodship JA, Burt AD, Flood TJ, Abinun M, Cant AJ, Johnson DS. Ommenn syndrome may be caused by mutations in the CHD7 gene. Clinical Genetics 2007, (submitted).
  • Matthews CJ, Green MA, Dunn AN, Flood TJ, Slatter MA, Gennery AR, Cant AJ, Carter V, Howell WM. MHC-associated polymorphism identification as an aid to determination of HLA haplotype identity in sibling HSC transplantation. International Journal of Immunogenetics 2007, 34(4), 298-299.
  • Gennery AR, Slatter MA, Bredius RG, Hagleitner MM, Weemaes C, Cant AJ, Lankester AC. Hematopoietic stem cell transplantation corrects the immunologic abnormalities associated with immunodeficiency-centromeric instability-facial dysmorphism syndrome. Pediatrics 2007, 120(5), E1341-E1344.
  • Haq IJ, Steinberg LJ, Hoenig M, van der Burg M, Villa A, Cant AJ, Middleton PG, Gennery AR. GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes. Clinical Immunology 2007, 124(2), 165-169.
  • Slatter M, Brigham K, Barge D, Jackson A, Flood T, Cant A, Abinun M, Gennery A. Comparison of immune reconstitution following anti-CD52 T-cell depleted haematopoietic stem cell transplant versus CD34+positive stem cell selection for SCID in a single centre. Bone Marrow Transplantation 2007, 39, S192-S192.
  • Thomas B, Flet JG, Shyam R, Kirk RC, Gennery AR, Spencer DA. Chronic respiratory complications in pediatric heart transplant recipients. Journal of Heart and Lung Transplantation 2007, 26(3), 236-240.
  • Larmouth W, Howard S, Abinun M, Slatter M, Gennery A. Bone marrow transplant for systemic lupus erythematosis; a case study. Bone Marrow Transplantation 2007, 39, S266-S266.
  • Slatter MA, Bhattacharya A, Flood TJ, Abinun M, Cant AJ, Gennery AR. Use of two unrelated umbilical cord stem cell units in stem cell transplantation for Wiskott-Aldrich syndrome. Pediatric Blood and Cancer 2006, 47(3), 332-334.
  • Evans PM, Woodbine L, Riballo E, Gennery AR, Hubank M, Jeggo PA. Radiation-induced delayed cell death in a hypomorphic Artemis cell line. Human Molecular Genetics 2006, 15(8), 1303-1311.
  • Gennery AR. Primary immunodeficiency syndromes associated with defective DNA double-strand break repair. British Medical Bulletin 2006, 77-78, 71-85.
  • Gallimore CI, Taylor C, Gennery AR, Cant AJ, Galloway A, Iturriza-Gomara M, Gray JJ. Environmental monitoring for gastroenteric viruses in a pediatric primary immunodeficiency unit. Journal of Clinical Microbiology 2006, 44(2), 395-399.
  • Crow YJ, Goodship JA, Wright C, Coady AM, Conley ME, Gennery AR. A newly recognized, likely autosomal recessive syndrome comprising agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis, and other features. American Journal of Medical Genetics Part A 2006, 140(11), 1131-1135.
  • Gallimore CI, Taylor C, Gennery AR, Cant AJ, Galloway A, Lewis D, Gray JJ. Use of a heminested reverse transcriptase PCR assay for detection of astrovirus in environmental swabs from an outbreak of gastroenteritis in a pediatric primary immunodeficiency unit. Journal of Clinical Microbiology 2005, 43(8), 3890-3894.
  • Bhattacharya A, Slatter MA, Chapman CE, Barge D, Jackson A, Flood TJ, Abinun M, Cant AJ, Gennery AR. Single centre experience of umbilical cord stem cell transplantation for primary immunodeficiency. Bone Marrow Transplantation 2005, 36(4), 295-299.
  • Slatter MA, Bhattacharya A, Abinun M, Flood TJ, Cant AJ, Gennery AR. Outcome of boost haemopoietic stem cell transplant for decresed donor chimerism or graft dysfunction in primary immunodeficiency. Bone Marrow Transplantation 2005, 35(7), 683-689.
  • Gennery AR, Hodges E, Williams AP, Harris S, Villa A, Angus B, Cant AJ, Smith JL. Omenn's syndrome occurring in patients without mutations in recombination activating genes. Clinical Immunology 2005, 116(3), 246-256.
  • Pan-Hammarstrom Q, Jones AM, Lahdesmaki A, Zhou W, Gatti RA, Hammarstrom L, Gennery AR, Ehrenstein MR. Impact of DNA ligase IV on nonhomologous end joining pathways during class switch recombination in human cells. Journal of Experimental Medicine 2005, 201(2), 189-194.
  • Slatter MA, Read S, Taylor CE, Crooks BNA, Abinun M, Flood TJ, Cant AJ, Wright C, Gennery AR. Adenovirus type F subtype 41 causing disseminated disease following bone marrow transplantation for immunodeficiency. Journal of Clinical Microbiology 2005, 43(3), 1462-1464.
  • Gennery AR, Khawaja K, Veys P, Bredius RGM, Notarangelo LD, Mazzolari E, Fischer A, Landais P, Cavazzana-Calvo M, Friedrich W, Fasth A, Wulffraat NM, Matthes-Martin S, Bensoussan D, Bordigoni P, Lange A, Pagliuca A, Andolina M, Cant AJ, Davies EG, European Grp for Blood and Bone Marrow Transplantation and the European Soc for Immunodeficiency. Treatment of CD40 ligand deficiency by hematopoietic stem cell transplantation: a survey of the European experience, 1993-2002. Blood 2004, 103(3), 1152-1157.
  • Slatter MA, Gennery AR, Cheetham TD, Bhattacharya TD, Crooks BNA, Flood TJ, Cant AJ, Abinun M. Thyroid dysfunction after bone marrow transplantation for primary immunodeficiency without the use of total body irradiation in conditioning. Bone Marrow Transplantation 2004, 33(9), 949-953.
  • Gennery AR, Slatter MA, Bhattacharya A, Barge D, Haigh S, O'Driscoll M, Coleman R, Abinun M, Flood TJ, Cant AJ, Jeggo PA. The clinical and biological overlap between Nijmegen Breakage Syndrome and Fanconi anemia. Clinical Immunology 2004, 113(2), 214-219.
  • Gennery AR, Spencer DA, Cant AJ. Immune Deficiency and the Lung. Current Paediatrics 2004, 14(2), 115-121.
  • Gennery AR, Thrasher A. Gene therapy for severe combined immunodeficiency. Current Anaesthesia and Critical Care 2004, 15(1), 3-9.
  • Gallimore CI, Lewis D, Taylor C, Cant A, Gennery A, Gray JJ. Chronic excretion of a recombinant norovirus in a child with cartilage hair hypoplasia (CHH). Journal of Clinical Virology 2004, 30(2), 196-204.
  • Gallimore CI, Lewis D, Taylor C, Cant A, Gennery A, Gray JJ. Chronic excretion of a norovirus in a child with cartilage hair hypoplasia (CHH). Journal of Clinical Virology 2004, 30(2), 196-204.
  • Riballo E, Kuhne M, Rief N, Doherty A, Smith GCM, Recio MJ, Reis C, Dahm K, Fricke A, Krempler A, Parker AR, Jackson SP, Gennery A, Jeggo PA, Lobrich M. A Pathway of Double-Strand Break Rejoining Dependent upon ATM, Artemis, and Proteins Locating to gamma-H2AX Foci. Molecular Cell 2004, 16(5), 715-724.
  • Bhattacharya A, Slatter M, Curtis A, Chapman CE, Barge D, Jackson A, Flood TJ, Abinun M, Cant AJ, Gennery AR. Successful umbilical cord blood stem cell transplantation for chronic granulomatous disease. Bone Marrow Transplantation 2003, 31(5), 403-405.
  • Slatter MA, Bhattacharya A, Flood TJ, Spickett GP, Cant AJ, Abinum M, Gennery AR. Polysaccharide antibody responses are impaired post bone marrow transplantation for severe combined immunodefiency, but not other primary immunodefeciencies. Bone Marrow Transplantation 2003, 32(2), 225-229.
  • Carrol ED, Gennery AR, Flood TJ, Spickett GP, Abinun M. Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO. Archives of Disease in Childhood 2003, 88(4), 340-341.
  • Krishna MT, Hodges E, Lavender FL, Harris S, Gennery A, Cant A, Gibson B, Wilkie R, Darbyshire P, Smith JL. CD3+CD4-CD8+NK- large granular lymphocytosis with neutropenia and evidence for clonality and T-Cell receptor gene rearrangement: Two pediatric cases. Journal of Pediatric Hematology / Oncology 2002, 24(6), 495-498.
  • Gennery AR, Barge D, O'Sullivan JJ, Flood TJ, Abinun M, Cant AJ. Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome. Archives of Disease in Childhood 2002, 86(6), 422-425.
  • Khawaja K, Gennery AR, Abinun M, Flood TJ, Cant AJ. Single Supraregional Centre Experience of Bone Marrow Transplantation for CD40L Deficiency. Archives of Disease in Childhood 2001, 84(6), 508-511.
  • Kane L, Gennery AR, Crooks BNA, Flood TJ, Abinun M, Cant AJ. Neonatal bone marrow transplantation for severe combined immunodeficiency. Archives of Disease in Childhood: Fetal and Neonatal Edition 2001, 85(2), F110-F113.
  • Gennery AR, Barge D, Spickett GP, Cant AJ. Lymphocyte subset populations in children with polysaccharide antibody deficiency following cardiac transplantation. Journal of Clinical Immunology 2001, 21(1), 37-42.
  • Kearns AM, Turner AJ, Taylor CE, George PW, Freeman R, Gennery AR. LightCycler™ - based quantitative PCR for the rapid detection of HHV-6 DNA in clinical material. Journal of Clinical Microbiology 2001, 39(8), 3020-3021.
  • O'Driscoll M, Cerosaletti KM, Girard PM, Dai Y, Stumm M, Kysela B, Hirsch B, Gennery A, Palmer SE, Seidel J, Gatti RA, Varon R, Oettinger MA, Neitzel H, Jeggo PA, Concannon P. DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency. Molecular Cell 2001, 8(6), 1175-1185.
  • Gennery AR, Cant AJ. Diagnosis of severe combined immunodeficiency. Journal of Clinical Pathology 2001, 54(3), 191-195.
  • Gennery AR, Cant AJ, Baldwin CI, Calvert JE. Characterization of the impaired antipneumococcal polysaccharide antibody production in immunosuppressed pediatric patients following cardiac transplantation. Journal of Clinical Immunology 2001, 21(1), 43-50.
  • Gennery AR, Dickinson AM, Brigham K, Barge D, Spickett GP, Curtis A, Spencer V, Jackson A, Cavanagh G, Carter V, Palmer P, Flood TJ, Cant AJ, Abinun M. CAMPATH-1M T-cell depleted BMT for SCID: Long-term follow-up of 19 children treated 1987-98 in a single center. Cytotherapy 2001, 3(3), 221-232.
  • Gennery AR, Dickinson AM, Brigham K, Barge D, Spickett GP, Curtis A, Spencer V, Jackson A, Carter V, Palmer P, Flood TJ, Cant AJ, Abinun M. CAMPATH-1M T-cell depleted BMT for SCID: long-term follow-up of 19 children treated 1987-98 in a single center. Cytotherapy 2001, 3(3), 221-232.
  • Khawaja K, Gennery AR, Flood TJ, Abinun M, Cant AJ. Bone marrow transplantation for CD40 ligand deficiency: a single centre experience. Archives of Disease in Childhood 2001, 84(6), 508-511.
  • Gennery AR, Cant AJ. Applied Physiology: Immune Competence. Current Paediatrics 2001, 11(6), 458-464.
  • Gennery AR, Flood TJ, Abinun M, Cant AJ. Bone marrow transplantation does not correct the hyper IgE syndrome. Bone Marrow Transplantation 2000, 25(12), 1303-1305.
  • Revy P, Muto T, Levy Y, Geissmann F, Plebani A, Sanal O, Catalan N, Forveille M, Dufourcq-Lagelouse R, Gennery A, Tezcan I, Ersoy F, Kayserili H, Ugazio AG, Brousse N, Muramatsu M, Notarangelo LD, Kinoshita K, Honjo T, Fischer A, Durandy A. Activation-Induced Cytidine Deaminase (AID) deficiency causes the autosomal recessive form of Hyper-IgM syndrome (HIGM2). Cell 2000, 102(5), 565-575.
  • Harwood JS, Gould FK, McMaster A, Hamilton JRL, Corris PA, Hasan A, Gennery AR, Dark JH. Significance of Epstein-Barr virus status and post-transplant lymphoproliferative disease I paediatric thoracic transplantation. Pediatric Transplantation 1999, 3(2), 100-103.
  • Kearns AM, Magee JG, Gennery A, Steward M, Graham C, Seiders PR, Freeman R. Rapid identification of Mycobacterium bovis BCG by the detection of the RD1 deletion using a multiplex PCR technique. International Journal of Tuberculosis and Lung Disease 1999, 3(7), 635-638.
  • Tweddle, D. A., Gennery, A. R., Reid, M. M., Thomas, J. A., Burke, M., Hamilton, J. R. L., Windebank, K. P. Posttransplantation B lymphoblastic leukemia with Burkitt-like features. Transplantation 1999, 67(10), 1379-1380.
  • Gennery AR, Hunter AS. Cross-sectional echocardiographic demonstration of duct-related intimal tissue plaques within the pulmonary artery. Cardiology in the Young 1999, 9(1), 81-83.
  • Gennery AR, O'Sullivan JJ, Hasan A, Hamilton JRL, Dark JH. Changing cyclosporin A formulation: an analysis in paediatric cardiac transplant recipients. Pediatric Transplantation 1999, 3(3), 215-218.
  • Gennery AR, Bartlett K, Hasan A. Thiamine deficiency mimicking acute rejection following cardiac transplantation. Cardiology in the Young 1998, 8(1), 113-115.
  • Billingham JL, Gennery A, Robinson JH, Spickett GP, Cant AJ. Immunological studies on children with the 22q11 deletion syndrome. Molecular Immunology 1998, 35(11-12), 737-737.
  • Gennery AR, Cant AJ, Spickett GP, Walshaw D, Hunter AS, Hasan A, Hamilton JRL, Dark JH. Effect of immunosuppression after cardiac transplantation in early childhood on antibody response to polysaccharide antigen. Lancet 1998, 351, 1778-1781.

• Book Chapters

  • van der Burg M, Gennery AR, Pan-Hammarstrom Q. Class-Switch Recombination Defects. In: D'Elios, M; Rizzi, M, ed. Humoral Primary Immunodeficiencies. Cham: Springer, 2019, pp.179-199.
  • Maggina P, Gennery AR. Primary immunodeficiency disorders: Diagnosis and management. In: Abutalib SA; Connors JM; Ragni MV, ed. Nonmalignant Hematology: Expert Clinical Review: Questions and Answers. Cham: Springer International Publishing, 2016, pp.575-584.
  • Gennery AR. Hematopoietic Stem Cell Transplantation for Primary Immunodeficiency. In: Stiehm's Immune Deficiencies. Amsterdam: Academic Press, 2014, pp.1007-1047.
  • Arkwright PD, Gennery AR. Ten warning signs of primary immunodeficiency: a new paradigm is needed for the 21st century. In: Casanova, J.L., Conley, M.E., Notarengelo, L, ed. The Year in Human and Medical Genetics: Inborn Errors of Immunity I. Oxford, UK: Wiley-Blackwell, 2011, pp.7-14.
  • Slatter MA, Gennery AR. Primary Immunodeficiency Syndromes. In: Diseases of DNA repair. Berlin, Germany: Springer, 2010, pp.146-165.
  • Gennery AR, Cant AJ. New Findings in Primary Immunodeficiency. In: Finn, A., Curtis, N., Pollard, A.J, ed. Hot Topics in Infection and Immunity in Children v. 5. New York, USA: Springer, 2009, pp.79-93.
  • Gennery AR, Cant AJ. New findings in primary immunodeficiency. In: Finn A; Curtis N; Pollard AJ, ed. Hot Topics in Infection and Immunity in Children V. New York: Springer, 2008, pp.79-94.
  • Gennery AR, Barge D, Spickett G. Immune recovery following hemopoietic stem cell transplant and vaccination. In: Cant, AJ; Galloway, A; Jackson, G, ed. Practical Hematopoietic Stem Cell Transplantation. Oxford: Blackwell Publishing, 2007, pp.140-146.
  • Gennery AR, Collin MP. Follow up in the first year after hemopoietic stem cell transplantation. In: Cant, AJ; Galloway, A; Jackson, G, ed. Practical Hematopoietic Stem Cell Transplantation. Oxford: Blackwell Publishing, 2007, pp.133-139.
  • Gennery AR, Finn AHR, Cant AJ. Primary and acquired immunodeficiency. In: Arceci, R., Hann, I., Smith, O, ed. Pediatric Hematology. Oxford: Blackwell Publishing, 2006, pp.425-449.
  • Gennery AR, Cant AJ. Respiratory Infection in the Immunocompromised Host: Recognition and Treatment. In: Kimpen, J.L.L., Ramilo, O, ed. The Microbe-Host Interface in Respiratory Tract Infections. Wymondham, UK: Horizon Scientific Press Ltd, 2005, pp.47-94.
  • Hambleton S, Gennery AR. Primay Immunodeficiency Syndromes, Defects of cellular and humoral immunity. In: Burg, F.D., Ingelfinger, J.R., Polin, R.A., Gershon, A.A, ed. Gellis and Kagan's Current Pediatric Therapy. WB Saunders, 2005. In Press.
  • Gennery AR, Cant AJ. Neonatal Infection: Immunology. In: Rennie, J.M, ed. Roberton’s Textbook of Neonatology. Edinburgh: Churchill Livingston, 2005, pp.Chapter 42.1.
  • Atherton DJ, Gennery AR, Cant AJ. The Neonate - Cutaneous features of primary immunodeficiency disorders. In: Burns, T., Griffiths, C., Cox, N., Breathnach, S, ed. Rook’s Textbook of Dermatology. Oxford, UK: Wiley-Blackwell, 2004, pp.chapter 14.
  • Cant AJ, Gibb D, Davies EG, Cale C, Gennery AR. Immunodeficiency. In: McIntosh, N., Helms, P., Smyth, R, ed. Forfar and Arneil’s Textbook of Pediatrics. Edinburgh, UK: Churchill Livingston, 2003, pp.chapter 25.

• Conference Proceedings (inc. Abstracts)

  • Offor UT, Long HM, Filby A, Ognjanovic M, Simmonds J, Parry G, Khushnood A, Reinhardt Z, Gennery AR, Bacon CM, Bomken S. Defining the systemic immune landscape in children at an increased risk of posttransplant lymphoproliferative disease: The immunology of thymectomy and childhood cardiac transplant (ITHACA) study. In: 7th International Symposium on Childhood, Adolescent and Young Adult Non-Hodgkin Lymphoma. 2022, New York, NY, USA: Leukemia Research.
  • Offor UT, Bacon C, Gennery A, Reinhardt Z, Bomken S. Cardiac transplantation for congenital heart disease is associated with an increased risk of post-transplant lymphoproliferative disorder (PTLD) in children: a single centre experience. In: 58th Annual Scientific Meeting of the British Society for Haematology. 2018, Liverpool, United Kingdom: British Journal of Haematology.
  • Offor UT, Bacon C, Gennery A, Reinhardt Z, Bomken S. An increased risk of post-transplant lymphoproliferative disorder in children after cardiac transplantation for congenital heart disease. In: 23rd Congress of the European Haematology Association. 2018, Stockholm, Sweden: Wolters Kluwer Health Inc.
  • Guest J, Cheal H, Lawrence J, Gennery A, Skinner R. The development of a Nurse-Led Clincal Apheresis service in extra-corporeal photopheresis (ECP) for the treatment of small body weight patients. In: 42nd Annual Meeting of the European Society for Blood and Marrow Transplantation. 2016, Valencia, Spain: Nature Publishing Group.
  • Dean HJ, McKean M, Gardner J, Pentland J, Vance G, Gennery A, Michaelis LJ. Respiratory acute life-threatening event (R-ALTE) reviews from Paediatric Intensive Care Unit (PICU) and the association with food allergy (FA) at Great North Children's Hospital (GNCH), Newcastle, UK - part 2. In: European Academy of Allergy and Clinical Immunology Congress. 2016, Vienna, Austria: Wiley-Blackwell Publishing Ltd.
  • Dean HJ, McKean M, Gardner J, Pentland J, Vance G, Gennery A, Michaelis LJ. Respiratory Acute Life-Threatening Event (R-ALTE) admissions to Paediatric Intensive Care Unit (PICU) and the association with Food Allergy (FA) at Great North Children's Hospital (GNCH), Newcastle, UK - Part 1. In: European Academy of Allergy and Clinical Immunology Congress. 2016, Vienna, Austria: Wiley-Blackwell Publishing Ltd.
  • Abd Hamid IJ, Slatter M, Pearce MS, Gennery A. Predictors of survival among individuals with severe combined immunodeficiency disorder undergoing hematopoietic stem cell transplantation. In: 42nd Annual Meeting of the European Society for Blood and Marrow Transplantation. 2016, Valencia, Spain: Nature Publishing Group.
  • Abd Hamid IJ, Slatter M, McKendrick F, Pearce MS, Gennery AR. Post-Transport health-related quality of life for different severe combined immunodeficiency genotypes. In: CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference. 2016, Boston, Massachusetts: Springer New York LLC.
  • Juliana I, Hamid A, Slatter M, McKendrick F, Pearce MS, Gennery A. Post-Transplant Health-Related Quality of Life for Different Severe Combined Immunodeficiency Genotypes. In: American Society of Pediatrics Hematology/Oncology (ASPHO). 2016, Minneapolis, MN, USA: Wiley-Blackwell Publishing Ltd.
  • Abd Hamid IJ, Slatter M, McKendrick F, Pearce MS, Gennery A. Post-transplant health-related quality of life for different severe combined immunodeficiency genotypes. In: 42nd Annual Meeting of the European Society for Blood and Marrow Transplantation. 2016, Valencia, Spain: Nature Publishing Group.
  • Saad A, Moczynski A, Sedlacek P, Albert MH, de Heredia CD, Smiers FJ, Bloomer J, Gennery AR, Inborn Error Working Party. Outcome of Alternative Donor Allogeneic Hematopoietic Stem Cell Transplantation in Erythpoietic Porphyria. In: 42nd Annual Meeting of the European Society for Blood and Marrow Transplantation. 2016, Valencia, Spain: Nature Publishing Group.
  • Abd Hamid IJ, Slatter M, Pearce MS, Gennery AR. Long-term immune reconstruction post-hematopoietic stem cell transplantation in IL2RG/JAK3 SCID, Newcastle experience. In: CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference. 2016, Boston, Massachusetts: Springer.
  • Abd Hamid IJ, Slatter M, Pearce MS, Gennery A. Long-term immune reconstitution post-hematopoietic stem cell transplantation in IL2RG/JAK3 SCID, Newcastle Experience. In: 42nd Annual Meeting of the European Society for Blood and Marrow Transplantation. 2016, Valencia, Spain: Nature Publishing Group.
  • Abd Hamid IJ, Slatter M, Pearce MS, Gennery A. Long-term immune reconstitution post- hematopoietic stem cell transplantation in IL2RG/JAK3 SCID, Newcastle experience. In: American Society of Pediatric Hematology/Oncology (ASPHO). 2016, Minneapolis, USA: John Wiley & Sons, Inc.
  • Abd Hamid IJ, Slatter M, Pearce MS, Gennery AR. A single centre cohort report of long term clinical outcome of severe combined immunodeficiency following haematopoietic stem cell transplantation. In: 2016 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference. 2016, Boston, Massachusetts, USA: Springer US.
  • Abd Hamid IJ, Slatter M, Pearce MS, Gennery A. A single centre cohort report of long term clinical outcome of severe combined immunodeficiency following haematopoietic stem cell transplantation. In: 42nd Annual Meeting of the European Society for Blood and Marrow Transplantation. 2016, Valencia, Spain: Nature Publishing Group.
  • Flinn A, Slatter M, Skinner R, Robson H, Cooper J, Guest J, Gennery A. A Retrospective Review of a Cohort of Paediatric Patients Treated with ECP for the Management of GVHD. In: 42nd Annual Meeting of the European Society for Blood and Marrow Transplantation. 2016, Valencia, Spain: Nature Publishing Group.
  • Abinun M, Lilic D, Devlin L, Christie S, Edgar D, Depner M, Fuchs S, Grimbacher B, Cant A, Flood T, Hambleton S, Gennery A, Nademi Z, Slatter M. Successful Allogeneic Haematopoietic Stem Cell Transplantation In A Child With Severe Immunodeficiency 31-C (OMIM # 614162) Due To STAT1-GOF Mutation. In: UKPIN 2015. 2015, Wiley-Blackwell.
  • Sarkar E, Barge D, Dockey D, Abinun M, Gennery A, Flood T, Blazina S, Lendem D, Lilic D. Long-term Lymphocyte Subset Monitoring In CMC Patients With gain-of-function STAT-1 Mutations. In: UKPIN 2015. 2015, Wiley-Blackwell.
  • Al Shehri T, Abinun M, Gennery AR, Rice GI, Crow YJ, Lilic D. Is Gain-of-function STAT1 CMC An Interferonopathy?. In: UKPIN 2015. 2015, Wiley-Blackwell.
  • Engelhardt KR, Xu YB, Grainger A, Batacchi MGCG, Swan DJ, Willet JDP, Abd Hamid IJ, Agyeman P, Barge D, Bibi S, Jenkins L, Flood T, Abinun M, Slatter M, Gennery AR, Cant AJ, Koref MS, Hambleton S. Identification Of Heterozygous Single- And Multi-exon Deletions In IL7R By Whole Exome Sequencing. In: UKPIN 2015 Meeting. 2015, Belfast, Northern Ireland: Wiley-Blackwell Publishing Ltd.
  • Morillo-Gutierrez B, Nademi Z, Dunn J, Barge D, Hambleton S, Abinun M, Flood T, Cant AJ, Gennery A, Slatter M. Haploidentical TCRab and CD19 Depleted Stem Cell Transplant for Primary Immunodeficiency-6 cases. In: 41st Annual Meeting of the European Society for Blood and Marrow Transplantation. 2015, Istanbul, Turkey: Nature Publishing Group.
  • Ferrua F, Courteille V, Janda A, Slatter M, Albert MH, Al-Mousa H, Al-Saud B, Balashov D, Bertrand Y, Booth C, Bordon V, Czogala W, Dogu F, Fasth A, Formankova R, Gozdzik J, Heilmann C, Honig M, Ikinciogullari A, Kalwak K, Keogh SJ, Krivan G, Lange A, Lankester AC, Ljungman P, Meyts I, Neven B, Soncini E, Suarez F, Mahlaoui N, Fischer A, Davies EG, Gennery AR, EBMT IEWP. Haematopoietic stem cell transplantation for CD40 ligand deficiency: results from an EBMT Inborn Errors Working Party (IEWP) study. In: 41st Annual Meeting of the European Society for Blood and Marrow Transplantation. 2015, Istanbul, Turkey: Nature Publishing Group.
  • Nademi Z, Gennery A, Dunn J, Slatter M. Treatment of steroid-refractory skin graft versus host disease with a CD3 TCR TCRαβ/CD19-depleted haplo-identical HSCT. In: 40th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2014, Milan, Italy: Nature Publishing Group.
  • Altmann T, Slatter M, Nademi Z, Abinun M, Gennery A. Treatment of steroid-refractory graft versus host disease (SR-GvHD) after bone marrow transplant (BMT) for primary immune deficiency-single centre experience. In: 40th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2014, Milan, Italy: Nature Publishing Group.
  • Battersby A, McKendrick F, Pearce MS, Cale C, Braggins H, Goldblatt D, Gennery AR. The Psychological Health of X-Linked Carriers of Chronic Granulomatous Disease (CGD) in the United Kingdom. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Battersby AC, Goldblatt D, Pearce MS, Braggins H, Cale C, Barge D, Gennery AR. The Health of Carriers of X-Linked Chronic Granulomatous Disease (CGD) in the United Kingdom. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Engelhardt KR, Gertz EM, Schaffer AA, Keles S, Sigmund EC, Ceja R, Sassi A, Graham L, Masaad MJ, Mellouli F, Ben-Mustapha I, Khemiri M, Kilic SS, Etzioni A, Freeman AF, Thiel J, Schulze I, Al-Herz W, Metin A, Sanal O, Tezcan I, Yeganeh M, Niehues T, Dueckers G, Weinspach S, Patiroglu T, Unal E, Dasouki M, Yilamaz M, Genel F, Aytekin C, Kutukculer N, Somer A, Kilic M, Reisli I, Camcioglu Y, Gennery AR, Cant AJ, Jones A, Gaspar HB, Arkwright PD, Pietrogrande MC, Baz Z, Al-Tamemi S, Lougaris V, Lefranc G, Megarbane A, Boutros J, Galal N, Bejaoui M, Barbouche MR, Geha RS, Chatila TA, Grimbacher B. The Extended Clinical Phenotype of 58 Patients with Dock8 Deficiency. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Flinn A, Abinun M, Leahy R, Cant A, Butler K, Gennery AR. STAT3-Deficient Hyper Ige Syndrome in a Pediatric Cohort. In: 2014 CIS Annual Meeting: Primary Immune Deficiency Diseases North American Conference. 2014, Baltimore, MD: Springer.
  • Morillo-Gutierrez B, Worth A, Slatter M, Nademi Z, Flood T, Valappil M, Waugh S, Breuer J, Gaspar B, Gennery A. Rotavirus Vaccine Serotype Infection in SCID Patients Following Introduction of Universal Rotavirus Vaccination in UK-4 Cases. In: 16th Biennial Meeting of the European Society for Immunodeficiences (ESID 2014). 2014, Prague, Czech Republic: Springer.
  • Battersby A, Pearce MS, Goldblatt D, Braggins H, Cale C, Gennery AR. Quality of Life (QOL) is Reduced in X-Linked Carriers of Chronic Granulomatous Disease (CGD). In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Mannurita SC, Vignoli M, Bacchetta R, Cecconi M, Tommasini A, Gennery AR, Cant AJ, Gambineri E. IPEX and 'IPEX-Like' Syndrome: FOXP3 and Related Pathway. In: 2014 CIS Annual Meeting: Primary Immune Deficiency Diseases North American Conference. 2014, Baltimore, MD: Springer US.
  • Slack J, Slatter MA, Gaspar B, Albert M, Ghosh S, Meisel R, Guengoer T, Karasu G, Drabko K, Lange A, Kalwak K, Pasic S, Heilmann C, Imai K, Shaw P, Schultz K, Eapen M, Horwitz E, Gennery AR, IEWP EBMT, CIBMTR. International study on outcomes of Haematopoietic Stem Cell transplant for DNA-DSB repair defects. In: 40th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2014, Milan, Italy: Nature Publishing Group.
  • Mannurita SC, Vignoli M, Colarusso G, Bacchetta R, Cecconi M, Tommasini A, Gennery A, Holland SM, Cant AJ, Gambineri E. Inherited Multiple Autoimmunity: Molecular and Clinical Characterization of IPEX and IPEX-Like Syndromes. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Abernethy K, Battersby A, Pearce MS, Barge D, Walter J, Notarangelo L, Cale C, Goldblatt D, Gennery A. Identification of Autoantibodies in Carriers of X-Linked Chronic Granulomatous Disease by Autoantigen Microarray Analysis. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Bigley V, Dickinson R, Jardine L, Milne PPS, Griffin H, Santibanez-Koref M, Haniffa M, Cant A, Hambleton S, Gennery A, Collin M. Human SHP-1 Mutation Causes an Autoinflammatory and Immunodeficiency Phenotype. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Battersby A, Martin A, Tarn J, Cale C, Goldblatt D, Gennery A. High Fatigue Levels in XL-CGD Carriers Associated with Raised Serum IL-8. In: ESID Meeting. 2014, Prague, Czech Republic: Springer.
  • Morillo-Gutierrez B, Nademi Z, Dunn J, Barge D, Hambleton S, Abinum M, Flood T, Cant AJ, Gennery AR, Slatter M. Haploidentical TCR Alfa/Beta and CD19 Depleted Stem Cell Transplant for Primary Immunodeficiency-4 Cases. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Harrison S, Slatter M, Nademi Z, Jolles S, Al-Herz W, Flood T, Cant A, Doffinger R, Glocker C, Grimbacher B, Abinun M, Gennery A. Haematopoietic Stem Cell Transplantation May Resolve the Immune Deficit Associated with STAT-3 Deficient Hyper-IGE Syndrome. In: 16th Biennial ESID Meeting 2014. 2014, Prague, Czech Republic: Springer.
  • Elfeky R, Nademi Z, Brigham K, Barge D, Hambleton S, Abinun M, Flood T, Cant A, Slatter M, Gennery A. Haematopoietic stem cell transplantation for RAG1/2 severe combined immunodeficiency or Omenn syndrome: a single centre experience. In: 40th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2014, Milan, Italy: Nature Publishing Group.
  • Ferrua F, Janda A, Courteille V, Slatter M, Albert MH, Al-Mousa H, Al-Saud B, Balashov D, Bertrand Y, Bordon V, Czogala W, Dogu F, Fasth A, Formankova R, Gozdzik J, Heilmann C, Honig M, Ikinciogullari A, Kalwak K, Keogh SJ, Krivan G, Lankester AC, Meyts I, Neven B, Suarez F, Mahlaoui N, Fischer A, Gennery AR. Haematopoietic Stem Cell Transplantation for CD40 Ligand Deficiency: Results from an EBMT/ESID Inborn Error Working Party Study. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Abinun M, Nademi Z, Flood TJ, Friswell M, Foster HE, Hambleton S, Gennery AR, Cant AJ, Slatter M. Haematopoietic stem cell transplantation (hsct) for severe autoimmune and autoinflammatory syndromes in children. In: 100th J Project Meeting. 2014, Antalya, TURKEY: Springer.
  • Zheng J, de Veerdonk FV, Crossland K, Smeekens SP, Abinun M, Gennery AR, Mann J, Lendrem D, Netea MG, Rowan AD, Lilic D. Gain-of-function stat1 mutation impairs stat3 function predisposing to chronic mucocutaneous candidiasis. In: 100th J Project Meeting. 2014, Antalya, TURKEY: Springer.
  • Walter JE, Rosen LB, Chen K, Lee YN, Tirosh I, Csomos K, Ujhazi B, Al-Herz W, Cowan MJ, Puck J, Bleesing JJ, Malech H, DeRavin SS, Gennery AR, Abraham RS, Butte MJ, Nadeau KC, Sullivan KE, Giliani S, Niehues T, Schuetz C, Kuijpers T, Holland SM, Browne SK, Notarangelo LD. Distinct Anti-Cytokine Autoantibody Profile is Likely Driven by Innate Hyperinflammation Among Patients with Primary Immunodeficiency Secondary To Rag Mutations. In: 2014 CIS Annual Meeting: Primary Immune Deficiency Diseases North American Conference. 2014, Baltimore, MD: Springer.
  • Felgentreff K, Du LK, Weinacht KG, Dobbs K, Bartish M, Giliani SC, Schlaeger TM, DeVine A, Schambach A, Woodbine L, Davies GE, Baxi SN, van der Burg M, Bleesing JJ, Gennery AR, Manis JP, Pan-Hammarstrom Q, Notarangelo LD. Differential Role for Dna Ligase 4, Artemis and Dna-Pkcs in the Generation, Dna Damage Response and Myeloid Differentiation of Human Ips Cells. In: 2014 CIS Annual Meeting: Primary Immune Deficiency Diseases North American Conference. 2014, Baltimore, MD: Springer.
  • Kharya G, Nademi Z, Leahy T, Brigham K, Barge D, Hambleton S, Abinun M, Flood T, Cant A, Slatter M, Gennery A. Common Gamma chain- and JAK3-deficient SCID, conditioned versus unconditioned transplant: a single centre experience. In: 40th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2014, Milan, Italy: Nature Publishing Group.
  • Ip W, Pitts A, Gaspar HB, Davies EG, Veys P, Slatter MA, Gennery AR, Qasim W. Clinical Presentation and Allogeneic Haematopoietic Stem Cell Transplantation in Cartilage Hair Hypoplasia. In: European Society for Immunodeficiencies. 2014, Prague, Czech Republic: Springer.
  • Lane J, Stewart C, Cummings S, Gennery A. Changes in the gut microbiome in severe combined immunodeficiency through haematopoietic stem cell transplantation. In: 40th Annual Meeting. 2014, Milan, Italy: Nature Publishing Group.
  • Worth AJJ, Nademi Z, Kammermeier J, Bunn S, Chiesa R, Cant A, Hambleton S, Shah N, Slatter M, Rao K, Gennery A, Elawad M, Amrolia P, Veys P. Allogeneic Stem Cell Transplant Offers Cure for Intractable Childhood Enteropathy. In: 2014 BMT Tandem Meetings. 2014, Dallas, Texas: Elsevier Inc.
  • O'Sullivan MD, Stroud C, Abinun M, Doffinger R, O'Reilly S, Ciechomska M, Barge D, Treacy R, Owens S, Flood T, Gennery A, Hambleton S. Late Onset Invasive Pneumococcal Disease in a Patient with IRAK4 Deficiency. In: AAAAI Annual Meeting. 2013, San Antonio, TX, USA: Mosby, Inc.
  • Griffin H, McDonald DO, Singh-Dang T, Dickinson R, Grainger A, Reynard L, Hussain R, Cant AJ, Gennery AR, Abinun M, Flood TJ, Collin MP, Loughlin J, Morgan NV, Santibanez-Koref M, Hambleton S. Whole exome sequencing as a diagnostic tool in primary immunodeficiency. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Slatter M, Rao K, Krol L, Sedlacek P, Nademi Z, Chiesa R, Amrolia P, Flood T, Abinun M, Cant A, Hambleton S, Gaspar H, Veys P, Gennery A. Treosulfan, fludarabine and alemtuzumab conditioning for haematopoietic stem cell transplantation in children with chronic granulomatous disease: experience in three centres. In: 38th Annual Meeting of the European Group for Blood and Marrow Transplantation (EBMT). 2012, Geneva, Switzerland: Nature Publishing Group.
  • Harkensee C, Oka A, Middleton PG, Gennery AR, Inoko H, Morishima Y. TNF-1031 single nucleotide polymorphism: An independent predictor of severe graft-versus-host disease?. In: 16th International HLA and Immunogenetics Workshop. 2012, Liverpool, UK: Wiley-Blackwell Publishing, Inc.
  • Madhra M, Mavin E, Grainger A, Barge D, Wang XN, Walter J, Matthew D, Notarangelo LD, Gennery A. Regulatory T cell subsets, T cell receptor repertoire, and autoantibodies in RAG1-deficient Omenn syndrome. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Sturgess K, Slatter M, Bigley V, Dickinson R, Haniffa M, McGovern N, Jardine L, Jackson G, Cant A, Gennery A, Hambleton S, Collin M. Reduced-intensity haematopoietic stem cell transplant rescues immune function and corrects pulmonary alveolar proteinosis in DCML deficiency/GATA 2 mutation. In: 38th Annual Meeting of the European Group for Blood and Marrow Transplantation (EBMT). 2012, Geneva, Switzerland: Nature Publishing Group.
  • Cole T, McKendrick F, Titman P, Cant AJ, Pearce MS, Cale CM, Goldblatt D, Gennery AR. Quality of life and emotional functioning in children with chronic granulomatous disease. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Maggina P, Nademi Z, Barge D, Hambleton S, Flood T, Cant AJ, Abinun M, Slatter M, Gennery A. Outcome of haematopoietic stem cell transplantation in patients with major histocompatibility class II deficiency at a national centre. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Lane J, Slatter M, Nademi Z, Tierney P, Barge D, Hambleton S, Flood T, Cant A, Abinun M, Jackson G, Collin M, Gennery A. Outcome of haematopoietic stem cell transplantation in patients with chronic granulomatous disease at a national centre. In: 38th Annual Meeting of the European Group for Blood and Marrow Transplantation (EBMT). 2012, Geneva, Switzerland: Nature Publishing Group.
  • Depner M, van de Veerdonk F, Wanders J, Stauss H, Raabe J, Atkinson TP, Schroeder HW, Niehues T, Duckers G, Puck J, Stray-Pedersen A, Baumann U, Schmidt R, Franco JL, Orrego J, Ben-Shoshan M, McCusker C, Jacob CMA, Carneiro-Sampaio M, Devlin LA, Edgar JD, Gkrania-Klotsas E, Kumararatne D, Doffinger R, Henderson P, Russell RK, Dyrso T, Seneviratne SL, Matthijs G, Abinun M, Gennery A, Johnson M, van der Meer JWM, Netea MG, Lilic D, Grimbacher B. Mutation screening in STAT1, CARD9 and PKC-DELTA in patients with chronic mucocutaneous candidiasis. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Harkensee C, Oka A, Middleton PG, Onizuka M, Gennery AR, Inoko H, Ando K, Morishima Y. Microsatellite scanning of the immunogenome for associations with hematopoietic stem cell transplantation outcomes. In: 16th International HLA and Immunogenetics Workshop. 2012, Liverpool, UK: Wiley-Blackwell Publishing, Inc.
  • Esteves I, Badawy S, Nademi Z, Barge D, Hambleton S, Flood T, Cant AJ, Abinun M, Slatter M, Gennery AR. Immunological reconstitution after haematopoietic stem cell transplantation for CD40L deficiency. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Moreira D, Slatter M, Nademi Z, Brigham K, Barge D, Jackson A, Flood T, Cant A, Abinun M, Hambleton S, Gennery A. Immune reconstitution and clinical outcome after HSCT infusion for severe combined immunodeficiency in Newcastle. In: Biology of Blood and Marrow Transplantation: BMT Tandem Meeting. 2012, San Diego, California, USA: Elsevier Inc.
  • Maggina P, Stroud C, Bourne H, Cole T, Collin M, Jackson G, Flood T, Barge D, Mansfield J, Hodges S, Spickett G, Gennery A. Idiopathic colitis following haematopoietic stem cell transplantation for chronic granulomatous disease: Three cases at a national centre. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Bigley V, Dickinson R, Gennery A, Griffin H, Haniffa M, McGovern N, Milne P, Cant A, Santibanez-Koref M, Hambleton S, Collin M. Human dendritic cell deficiency. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Gambineri E, Mannurita SC, Robertson H, Vignoli M, Hambleton S, Gennery A, Slatter M, Nademi Z, Barge D, Abinun M, Cant AJ. Gut Immune Reconstitution in IPEX Syndrome After HSCT. In: Annual Meeting of the Clinical Immunology Society (CIS). 2012, Chicago, Illinois, USA: Springer.
  • Mannurita SC, Robertson H, Vignoli M, Hambleton S, Gennery AR, Slatter M, Nademi Z, Barge D, Abinun M, Cant AW, Gambineri E. Gut immune reconstitution in Ipex Syndrome after HSCT. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer New York LLC.
  • Zheng J, Rowan AD, Gennery AR, Abinun M, Lilic D, Primary Immune Deficiency Grp, Inst Cellular Med. Gain-of-function STAT1 mutations alter STAT3 activation in patients with chronic mucocutaneous candidiasis. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer New York LLC.
  • Lombardo A, Firrito C, Lo Riso P, Gennery AR, Di Stefano B, Broccoli V, Holmes MC, Gregory PD, Naldini L. Efficient Generation of Gene-Corrected, Vector- and Reprogramming Factor-Free iPS Cells from SCID-X1 Patients. In: 15th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT). 2012, Philadelphia, Pennsylvania, USA: Nature Publishing Group.
  • Lombardo A, Firrito C, Gennery AR, Holmes MC, Gregory PD, Naldini L. Efficient generation of gene-corrected and reprogramming factor-free iPS cells from SCID-X1 patients. In: Collaborative Congress of the European Society of Gene and Cell Therapy. 2012, Versailles, France: Mary Ann Liebert, Inc. Publishers.
  • Engelhardt KR, Gertz EM, Keles S, Schaffer AA, Ceja R, Sassi A, Massaad MJ, Mellouli F, Benmustapha I, Khemiri M, Kilic SS, Etzioni A, Freeman AF, Thiel J, Schulze I, Al-Herz W, Metin A, Sanal O, Yeganeh M, Niehues T, Siepermann K, Unal E, Patiroglu T, Dasouki M, Yilmaz M, Genel F, Aytekin C, Kutukculer N, Somer A, Kilic M, Reisli I, Camcioglu Y, Gennery AR, Cant AJ, Jones A, Gaspar HB, Arkwright PD, Pietrogrande MC, Baz Z, Al-Tamemi S, Lougaris V, Lefranc G, Megarbane A, Boutros J, Galal N, Bejaoui M, Barbouche R, Geha RS, Chatila TA, Grimbacher B. Dock8 deficiency and a diagnostic score to differentiate it from other hyper-IgE syndromes. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Colarusso G, Mannurita SC, Vignoli M, Barzaghi F, Passerini L, Cancrini C, Cant A, Gennery A, Abinun M, Ikinciogullari A, Lionetti P, Bacchetta R, Gambineri E. Clinical analysis of the complex world of inherited multiple autoimmunity. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Barge D, Bainbridge M, Slatter M, Gennery A, Hambleton S, Abinun M, Flood T, Cant A, Spickett G. Class switch memory B cells in assessing humoral immunity post HSCT for primary immune deficiency. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Hambleton S, McDonald DO, Morgan NV, Griffin H, Singh-Dang T, Grainger A, Reynard L, Gennery AR, Slatter M, Flood TJ, McKiernan P, Barge D, Abinun M, Hackett S, Loughlin J, Lakey J, Cant AJ, Santibanez-Koref M. Autosomal recessive combines immunodeficiency due to loss of function mutation in Tripeptidyl Peptidase II. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Felgentreff K, Weinacht KG, Gennery AR, Dobbs K, Giliani S, Matzig T, Schambach A, Baum C, Notarangelo LD. Artemis and ligase 4 are dispensable for the generation of human induced pluripotent stem cells. In: 5th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
  • Sturgess K, Slatter M, Bigley V, Haniffa M, Wang XN, Dickinson R, McGovern N, Jardine L, Pagan S, Chua I, Wallis J, Lordan J, Morgan C, Cant A, Gennery A, Edmondson R, Bacon C, Black F, Kirkham N, Jackson GH, Hambleton S, Collin MP. Reduced Intensity Hematopoietic Stem Cell Transplant Rescues Immune Function and Corrects Pulmonary Alveolar Proteinosis in DCML Deficiency/GATA 2 Mutation. In: Blood: 53rd Annual Meeting and Exposition of the American Society of Hematology (ASH). 2011, San Diego, California, USA: American Society of Hematology.
  • Elemraid MA, Eastham KM, Rushton SP, Shirley MDF, Spencer DA, Thomas MF, Hampton F, Gorton R, Pollard K, Gennery AR, Clark JE. Impact of heptavalent pneumococcal conjugate vaccine on the incidence of childhood pneumonia seen in hospital in the North East of England. In: Thorax: Winter Meeting of the British Thoracic Society. 2011, Westminster: BMJ Group.
  • Lane JP, Evans PTG, Slatter MA, Barge D, Jackson A, Hambleton S, Flood T, Abinun M, Cant J, Gennery A. Immune reconstitution post umbilical cord blood stem cell transplantation for primary immunodeficiency in a national centre. In: Bone Marrow Transplantation: 37th European Group for Bone and Marrow Transplantation. 2011, Paris, France: Nature Publishing Group.
  • Evans P, Lane JP, Slatter MA, Barge D, Jackson A, Hambleton S, Flood TJ, Abinun M, Cant AJ, Gennery AR. EFFECT OF SEROTHERAPY DOSE ON IMMUNORECONSTITUTION FOLLOWING UMBILICAL CORD STEM CELL TRANSPLANT FOR PRIMARY IMMUNODEFICIENCY. In: PEDIATRIC RESEARCH. 2011, 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA: NATURE PUBLISHING GROUP.
  • Elemraid MA, Eltringham G, Sails AD, Perry J, Thomas MF, Spencer DA, Eastham KM, Shirley MD, Rushton SP, Hampton F, Gorton R, Gennery AR, Clark JE, North East England Paediatr Resp I. CLINICAL SIGNIFICANCE OF INFLAMMATORY MARKERS AND RADIOLOGICAL FEATURES IN PREDICTING THE AETIOLOGY OF COMMUNITY-ACQUIRED PNEUMONIA IN CHILDREN. In: PEDIATRIC RESEARCH. 2011, 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA: NATURE PUBLISHING GROUP.
  • Slatter M, Rao K, Amrolia P, Flood T, Abinun M, Cant A, Hambleton S, Goulden N, Davies G, Qasim W, Gasper HB, Gennery A, Veys P. UK experience of treosulfan-based conditioning regimens in children with primary immunodeficiency. In: 36th Annual Meeting of the European Group for Blood and Marrow Transplantat/9th Meeting of the EBMT Data Management Group/26th Meeting of the EBMT Nurses Group/2nd EBMT Quality Management Meeting. 2010, Vienna, Austria: Bone Marrow Transplantation, Nature Publishing Group.
  • Slatter M, Nademi Z, Patel S, Barge D, Valappil M, Brigham K, Hambleton S, Flood T, Cant A, Abinun M, Gennery A. Transplantation of CD3/CD19 depleted PBSC leading to viral clearance and no graft-versus-host disease in SCID. In: 36th Annual Meeting of the European Group for Blood and Marrow Transplantat/9th Meeting of the EBMT Data Management Group/26th Meeting of the EBMT Nurses Group/2nd EBMT Quality Management Meeting. 2010, Vienna, Austria: Bone Marrow Transplantation, Nature Publishing Group.
  • Nademi Z, Slatter M, Barge D, Hodges S, Bunn S, Thomas J, Harvey H, Hambleton S, Flood T, Cant A, Abinun M, Gennery A. Single-centre experience of haematopoeitic stem cell transplantation for patients with complex autoimmune enteropathies. In: 36th Annual Meeting of the European Group for Blood and Marrow Transplantation/9th Meeting of the EBMT Data Management Group/26th Meeting of the EBMT Nurses Group/2nd EBMT Quality Management Meeting. 2010, Vienna, Austria: Bone Marrow Transplantation, Nature Publishing Group.
  • Woellner C, Gertz ME, Schaffer AA, Lagos M, Perro M, Glocker EO, Pietrogrande MC, Cossu F, Franco JL, Matamoros N, Pietrucha B, Heropolitanska-Pliszka E, Yeganch M, Moin M, Espanol T, Ehl S, Gennery AR, Abinun M, Breborowicz A, Niehues T, Kilic SS, Junker A, Turvey SE, Plebani A, Sanchez B, Garty BZ, Pignata C, Cancrini C, Litzman J, Sanal O, Batimann U, Bacchetta R, Hsu AP, Davis JN, Hammarstrom L, Davies GE, Eren E, Arkwright PD, Moilanen JS, Viemann D, Khan S, Marodi L, Cant AJ, Freeman AF, Puck JM, Holland SM, Grimbacher B. Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome. In: Clinical and Experimental Immunology: United Kingdom Primary Immunodeficiency Network Immunology Forum. 2010, Bath, UK: Wiley-Blackwell Publishing Ltd.
  • Vignoli M, Mannurita SC, Bianchi L, Bacchetta R, Cecconi M, Tommasini A, Abinun M, Gennery A, Hambleton S, Slatter M, Cant A, de Martino M, Gambineri E. Exploring 'IPEX-like Syndrome': What is Beyond FOXP3 Gene?. In: 10th Annual Meeting of the Federation of Clinical Immunology Societies. 2010, Boston, MA: Clinical Immunology, Academic Press.
  • Morgan NV, Goddard S, Cardno TS, Rahman F, Crupek A, Straatman-Iwanowska A, Pasha S, Hambleton S, Cant A, Barge D, Gennery A, McDonald D, Anderson G, Huissoon A, Tate WP, Maher ER. A novel human immunodeficiency disorder associated with a mutation in the T cell receptor a subunit constant gene (TRAC). In: Clinical and Experimental Immunology: United Kingdom Primary Immunodeficiency Network Immunology Forum. 2010, Bath, UK: British Society for Immunology.
  • Slatter M, Ferguson C, Rogerson E, Yurasova A, Askew P, Flood T, Abinun M, Cant A, Bunn S, Thomas J, Gennery A. Nutritional assessment of children undergoing haematopoietic stem cell transplantation for primary immunodeficiency or severe autoimmune disease. In: Bone Marrow Transplantation: 35th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2009, Goteborg, Sweden: Nature Publishing Group.
  • Slatter M, Windebank K, Angus B, Barborie A, Perry A, Lester T, Norbury G, Abinun M, Flood T, Cant A, Gennery A. Malignancy as a presentation of common gamma chain deficient severe combined immunodeficiency. In: Bone Marrow Transplantation: 35th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2009, Goteborg, Sweden: Nature Publishing Group.
  • Albert MH, Gennery AR, Greil J, Cale CM, Kondratenko I, Notheis G, Fuhrer M, Belohradsky BH. Stem cell transplantation for Nijmegen breakage syndrome experience in five patients. In: Clinical and Experimental Immunology: 13th European Society for Immunodeficiencies. 2008, sHertogenbosch, The Netherlands: Wiley-Blackwell Publishing Ltd.
  • Janda AJ, Sedlacek P, Sediva A, Honig M, Friedrich W, Champagne M, Matsumoto T, Fischer A, Neven B, Contet A, Bensoussan D, Bordigoni P, Davies G, Loeb D, Savage W, Jabado N, Bonilla F, Gennery AR. Multicentric survey on outcome of transplantation of hematopoetic cells in severely immunodeficient patients with complete form of DiGeorge syndrome. In: Clinical and Experimental Immunology: 13th European Society for Immunodeficiencies. 2008, sHertogenbosch, The Netherlands: Wiley-Blackwell Publishing Ltd.
  • Slatter M, Windebank K, Angus B, Dildey P, Barborie A, Perry R, Lester T, Norbury G, Abinun M, Flood TJ, Cant AJ, Gennery AR. Malignancy as a presentation of common gamma chain deficient severe combined immunodeficiency. In: 13th Meeting of the European Society for Immunology. 2008, Theater aan de Parade, 's-Hertogenbosch, the Netherlands: Clinical and Experimental Immunology: Wiley-Blackwell.
  • Bordon V, Gennery AR, Slatter MR, Vandecruys E, Laureys G, Veys P, Amrolia P, Scherer F, Cant A, Gungor T. Haematopoietic stem cell transplantation in patients with cartilage hair hypoptasia. In: Clinical and Experimental Immunology: 13th European Society for Immunodeficiencies. 2008, sHertogenbosch, The Netherlands: Wiley-Blackwell Publishing Ltd.
  • Soncini E, Slatter M, Jones L, Hughes S, Flood T, Barge D, Spickett GP, Jackson GH, Collin M, Abinun M, Cant AJ, Gennery AR. Haematopoeitic stem cell transplantation for chronic granulomatous disease - a single-centre experience. In: 34th Annual Meeting of the European Group for Blood and Marrow Transplantation (EBMT 2008). 2008, Florence, Italy: Bone Marrow Transplantation: Nature Publishing Group.
  • Abinun M, Jolles S, Hare BO, Jenney M, Barton J, Doffinger R, Kumararatne DS, Flood TJ, Gennery AR, Clark J, Slatter M, Hughes S, Cant AJ. EDA-ID due to NEMO mutation complicated by disseminated mycobacterium infection: successful haematopoietic stem cell transplantation. In: 13th Meeting of the European Society for Immunology. 2008, Theater aan de Parade, 's-Hertogenbosch, the Netherlands: Clinical and Experimental Immunology: Wiley-Blackwell.
  • Woellner C, Gertz EM, Schaeffer AA, Lagos M, Perro M, Pietrogrande MC, Cossu F, Franco JL, Matamoros N, Pietrucha B, Heropolianska-Pliszka E, Yeganeh M, Espanol T, Ehl S, Gennery AR, Abinun M, Breborowicz A, Niehues T, Kilic SS, Junker A, Turvey S, Plebani A, Sanchez B, Garty BZ, Pignata C, Cancrini C, Litzman J, Sanal O, Baumann U, Bacchetta R, Hsu A, Hammarstrom L, Davies EG, Eren E, Arkwright PD, Moilanen JS, Viemann D, Khan S, Marodi L, Cant AM, Puck JM, Holland SM, Grimbacher B. Diagnostic criteria for the hyper IgE recurrent infection syndrome/Job's syndrome/STAT3 deficiency. In: 13th Meeting of the European Society for Immunology. 2008, Theater aan de Parade, 's-Hertogenbosch, the Netherlands: Clinical and Experimental Immunology: Wiley-Blackwell.
  • Breese G, Gennery AR, Zwolinski SA. Case report of two siblings with ICF syndrome. In: Journal of Medical Genetics: British Human Genetics Conference. 2008, University of York, UK: BMJ Group.
  • Gennery AR, Robinson H, Slatter MA, Barge D, Bown N, Jackson A, Harvey H, Flood TJ, Cant AJ, Abinun M. Assessment of reduced intensity conditioning regimens for haematopoietic stem cell transplantation in primary immunodeficiency. In: 13th Meeting of the European Society for Immunology. 2008, Theater aan de Parade, 's-Hertogenbosch, the Netherlands: Clinical and Experimental Immunology: Wiley-Blackwell.
  • Taha Y, Taylor C, Gennery A, Abinun M, Flood T, Clarke J, Al-Aufi N, Al-Husamy H, Cant A. Human herpesvirus-6 viraemia in children with primary immunodeficiency undergoing stem-cell-transplantation. In: 9th Annual Meeting of the European Society for Clinical Virology/Society for General Microbiology Clinical Virology Group. 2006, Birmingham, UK: Journal of Clinical Virology: Elsevier.
  • Ridley A, Hodges E, Harris S, Gilmour K, Vance G, Gennery A, Cant A, Jones A, Davis G, Krishna M, Gnanakurmaran G, Smith J. Gamma delta lymphocytoses in primary immunodeficiency (PID): A case series analysis. In: Clinical Immunology: 6th Annual Meeting of the Federation of Clinical Immunology Societies. 2006, San Francisco, CA: Academic Press.
  • Moss SJ, Gennery AR. Controversies in neonatal sepsis: Immunomodulation in the treatment and prevention of neonatal sepsis. In: Hot Topics in Infection and Immunity in Children III. 2006, Oxford, UK: Springer.
  • Gennery AR, Slatter MA, Clark JE, Barge D, Wood P, Rieux-Laucat F, Cant AJ. Manifestations of autoimmune lymphoproliferative syndrome. In: Immunology: Annual Congress of the British Society for Immunology. 2005, Harrogate, UK: Wiley-Blackwell Publishing Ltd.
  • Ridley AL, Hodges E, Harris S, Vance G, Gennery A, Cant A, Jones A, Davis G, Krishna MT, Smith JL. Gamma delta lymphocytosis in primary immunodeficiency (PID): a case series analysis. In: Immunology: Annual Congress of the British Society for Immunology. 2005, Harrogate, UK: Wiley-Blackwell Publishing Ltd.
  • Hodges E, Gennery AR, Harris S, Smith JL. Expansion of maternally derived monoclonal T cells with a CD3+CD8+TCR gamma delta phenotype in two children with severe combined immunodeficiency. In: Clinical Immunology: 5th Annual Meeting of the Federation of Clinical Immunology Society. 2005, Boston, Massachusetts, USA: Academic Press.
  • Rogerson E, Larmouth W, Slatter M, Taylor C, Gennery A. CMV in the transplant patient. In: Bone Marrow Transplantation: 31st Annual Meeting of the European Group for Blood and Marrow Transplantation. 2005, Prague, Czech Republic: Nature Publishing Group.
  • Gennery A, Slatter M, Barge D, Flood T, Hodges S, Cant AJ, Abinun M. Bone marrow transplantation for IPEX-like syndrome. In: Immunology: Annual Congress of the British Society for Immunology. 2005, Harrogate, UK: Wiley-Blackwell Publishing Ltd.
  • Bhattacharya A, Slatter MA, Chapman CE, Barge D, Flood TJ, Abinun M, Cant AJ, Gennery AR. Use of two unrelated umbilical cord stem cell units in stem cell transplantation for Wiskott Aldrich syndrome. In: 30th Annual Meeting of the European Group for Blood and Marrow Transplantation/20th Meeting of the EBMT Nurses Group/3rd Meeting of the EBMT Data Management Group. 2004, Barcelona, Spain: Bone Marrow Transplantation: Nature Publishing Group.
  • Gennery AR, Cant AJ. The immunocompromised host: The patient with recurrent infection. In: Hot Topics in Infection and Immunity in Children. 2004, Oxford, UK: Springer.
  • Gennery AR, Bhattacharya A, Slatter MA, Flood TJ, Abinun M, Breese GJ, Cant AJ. Successful bone marrow transplantation for immunodeficiency, centromere instability and facial anomalies syndrome. In: Bone Marrow Transplantation: 30th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2004, Barcelona, Spain: Nature Publishing Group.
  • Slatter MA, Bhattacharya A, Abinun M, Flood TJ, Cant AJ, Gennery AR. Outcome of boost haemopoietic stem cell transplant for decrease in donor chimerism or graft dysfunction in primary immunodeficiency. In: 30th Annual Meeting of the European Group for Blood and Marrow Transplantation/20th Meeting of the EBMT Nurses Group/3rd Meeting of the EBMT Data Management Group. 2004, Barcelona, Spain: Bone Marrow Transplantation: Nature Publishing Group.

• Editorials

  • Gennery AR. The “B” side of IL-7Rα–deficient SCID. Blood 2023, 142(13), 1105-1106.
  • Gennery AR, Gonzalez-Granado LI, Torgerson TR. Editorial: Primary immune regulatory disorders: Coming of age. Frontiers in Pediatrics 2023, 11, 1155785.
  • Elliman DAC, Gennery AR. Newborn screening for severe combined immunodeficiency—Coming to a region near you soon. Clinical and Experimental Immunology 2021, 205(3), 343-345.
  • Gennery AR. The sting of WASP deficiency: autoimmunity exposed. Blood 2016, 127(2), 173-175.
  • Gennery AR. The Evolving Landscape of Primary Immunodeficiencies. Journal of Clinical Immunology 2016, 36(4), 339-340.
  • Gennery AR. Gene therapy for PID: the end of the beginning?. Blood 2016, 128(1), 7-8.
  • Gennery AR. Severe Infections in Patients With Chronic Granulomatous Disease. Clinical Infectious Diseases 2015, 60(8), 1184-1185.
  • Gennery AR, Holland SM. Primary immunodeficiencies: not just paediatric diseases. European Respiratory Journal 2015, 45(6), 1521-1523.
  • Laberko A, Gennery AR. Cytoreductive conditioning for severe combined immunodeficiency - help or hindrance?. Expert Review of Clinical Immunology 2015, 11(7), 785-788.
  • Gennery AR, Slatter MA. Chemotherapy-free conditioning: one step closer. Blood 2014, 124(6), 838-840.
  • Maggina P, Gennery AR. Classification of primary immunodeficiencies: Need for a revised approach?. Journal of Allergy and Clinical Immunology 2013, 131(2), 292-294.
  • Brown L, Xu-Bayford J, Allwood Z, Slatter M, Cant A, Davies EG, Veys P, Gennery AR, Gaspar HB. Neonatal Diagnosis of Severe Combined Immunodeficiency Leads to Significantly Improved Survival Outcome: The Case for Newborn Screening [editorial comment]. Obstetrical & Gynecological Survey 2011, 66(7), 398-399.
  • Harkensee C, Vasdev N, Gennery AR, Willetts IE, Taylor C. Commentary to "Pediatric hemorrhagic cystitis" by Decker DB, Karam JA, Wilcox DT. J Pediatr Urol 2009;5:254-264 Management of hemorrhagic cystitis in children after hematopoietic stem cell transplantation: Keep it safe. Journal of Pediatric Urology 2010, 6(1), 96-97.
  • Gennery AR, O'Driscoll M. Unravelling the web of DNA repair disorders. Clinical and Experimental Immunology 2003, 134(3), 385-387.
  • Gennery AR, Cant AJ. Development of allergy post-bone marrow transplantation. Clinical and Experimental Allergy 2002, 32(12), 1677-1678.

• Letters

  • Ramanathan S, Roberts W, Nademi Z, Shenton G, Watson H, Matthews E, Carruthers K, Gennery AR, Hambleton S, Slatter M, Lum SH. CD3+TCRαβ/CD19+-depleted stem cell boost and CD45RO+ memory T-cell add-back as a successful salvage treatment for poor graft function unresponsive to eltrombopag, following a second allogenic HSCT. Pediatric Blood and Cancer 2024, ePub ahead of Print.
  • Roderick MR, Jefferson L, Renton W, Belot A, Ramanan AV, Jolles S, Bernatoniene J, Mathieu A-L, Buxton C, Gennery AR. Compound Heterozygous Mutations in PRKCD Associated with Early-Onset Lupus and Severe and Invasive Infections in Siblings. Journal of Clinical Immunology 2023, 43, 703–705.
  • Carruthers V-A, Lum SH, Flood T, Slatter MA, Gennery AR. Hematopoietic Cell Transplant for CD40 Ligand Deficiency—Comparing Busulfan Versus Treosulfan. Journal of Clinical Immunology 2022, 42, 703-705.
  • Shiraki M, Williams E, Yokoyama N, Shinoda K, Nademi Z, Matsumoto K, Nihira H, Honda Y, Izawa K, Nishikomori R, Slatter MA, Cant AJ, Gennery AR, Ohnishi H, Kanegane H. Hematopoietic Cell Transplantation Ameliorates Autoinflammation in A20 Haploinsufficiency. Journal of Clinical Immunology 2021, 41, 1954–1956.
  • Hurst JR, Abbas SH, Bintalib HM, Alfaro TM, Baumann U, Burns SO, Condliffe A, Davidsen JR, Fevang B, Gennery AR, Haerynck F, Jacob J, Jolles S, Lamers O, Bergeron A, Malphettes M, Meignin V, Milito C, Milota T, Pergent M, Prasse A, Quinti I, Renzoni E, Sediva A, Stolz D, Smits B, Strauss F, Van De Ven Annick AJM, Van Montfrans J, Warnatz K. Granulomatous-lymphocytic interstitial lung disease: An international research prioritisation. ERJ Open Research 2021, 7(4), 00467-2021.
  • Flinn AM, Flood T, Prendiville T, Gennery AR, Leahy TR. Adenosine Deaminase Deficient SCID with Myocardial Hypertrophy. Journal of Clinical Immunology 2021, 41, 1128-1130.
  • Lum SH, Flood T, Hambleton S, McNaughton P, Watson H, Abinun M, Owens S, Cigrovski N, Cant A, Gennery AR, Slatter M. Two decades of excellent transplant survival for chronic granulomatous disease: A supraregional immunology transplant center report. Blood 2019, 133(23), 2546-2549.
  • Battersby AC, Martin AJ, Tarn J, Ng WF, Cale CM, Goldblatt D, Gennery AR. Raised Serum IL-8 Levels Are Associated with Excessive Fatigue in Female Carriers of X-Linked Chronic Granulomatous Disease in the UK. Journal of Clinical Immunology 2017, 37(3), 279-281.
  • Tsilifis C, Gennery AR, Cant A. Presenting features and platelet anomalies in WAS: one centre’s experience. Journal of Clinical Immunology 2016, 36(4), 354-356.
  • Slatter MA, Engelhardt KR, Burroughs LM, Arkwright PD, Nademi Z, Skoda-Smith S, Hagin D, Kennedy A, Barge D, Flood T, Abinun M, Wynn RF, Gennery AR, Cant AJ, Sansom D, Hambleton S, Torgerson TR. Hematopoietic stem cell transplantation for CTLA4 deficiency. Journal of ALlergy and Clinical Immunology 2016, 138(2), 615-619.
  • Slatter M, Nademi Z, Leahy TR, Morillo-Gutierrez B, Dunn J, Barge D, Skinner R, Ryan C, Hambleton S, Abinun M, Flood T, Cant A, Gennery A. Haploidentical CD3 TCRαβ and CD19-depleted second stem cell transplant for steroid-resistant acute skin graft versus host disease. Journal of Allergy and Clinical Immunology 2016, 138(2), 603-605.
  • Lane JP, Stewart CJ, Cummings SP, Gennery AR. Functional changes in gut microbiota during hematopoietic stem cell transplantation for severe combined immunodeficiency. Journal of Allergy and Clinical Immunology 2016, 138(2), 622-625.
  • Flinn AM, Cant A, Leahy TR, Butler KM, Gennery AR. Autosomal Dominant Hyper IgE Syndrome - Treatment Strategies and Clinical Outcomes. Journal of Clinical Immunology 2016, 36(2), 107-109.
  • Mather MW, Hayhurst H, Bacon CM, Cole TS, Pan-Hammarstrom Q, Misbah S, Gennery AR. Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation. Journal of Allergy and Clinical Immunology 2015, 135(2), 559-561.
  • Lane JP, Stewart CJ, Cummings SP, Gennery AR. Gut microbiome variations during hematopoietic stem cell transplant in severe combined immunodeficiency. Journal of Allergy and Clinical Immunology 2015, 135(6), 1654-1656.
  • Gambineri E, Mannurita SC, Robertson H, Vignoli M, Haugk B, Lionetti P, Hambleton S, Barge D, Gennery AR, Slatter M, Nademi Z, Flood TJ, Jackson A, Abinun M, Cant AJ. Gut immune reconstitution in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome after hematopoietic stem cell transplantation. Journal of Allergy and Clinical Immunology 2015, 135(1), 260-262.e8.
  • Morillo-Gutierrez B, Worth A, Valappil M, Gaspar HB, Gennery AR. Chronic Infection with Rotavirus Vaccine Strains in UK Children with Severe Combined Immunodeficiency. Pediatric Infectious Disease Journal 2015, 34(9), 1040-1041.
  • Nademi Z, Slatter M, Gambineri E, Mannurita SC, Barge D, Hodges S, Bunn S, Thomas J, Haugk B, Hambleton S, Flood T, Cant A, Abinun M, Gennery A. Single centre experience of haematopoietic SCT for patients with immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. Bone Marrow Transplantation 2014, 49(2), 310-312.
  • Kharya G, Nademi Z, Leahy TR, Dunn J, Barge D, Schulz A, Cant A, Gennery A, Slatter M. Haploidentical T-cell alpha beta receptor and CD19-depleted stem cell transplant for Wiskott-Aldrich syndrome. Journal of Allergy and Clinical Immunology 2014, 134(5), 1199-1201.
  • Slatter M, Nademi Z, Patel S, Barge D, Valappil M, Brigham K, Hambleton S, Clark J, Flood T, Cant A, Abinun M, Gennery A. Haploidentical hematopoietic stem cell transplantation can lead to viral clearance in severe combined immunodeficiency. Journal of Allergy and Clinical Immunology 2013, 131(6), 1705-1708.e1.
  • Bacon CM, Wilkinson SJ, Spickett GP, Barge D, Lucraft HH, Jackson G, Rand V, Gennery AR. Epstein-Barr virus-independent diffuse large B-cell lymphoma in DNA ligase 4 deficiency. Journal of Allergy and Clinical Immunology 2013, 131(4), 1237-1239.
  • Cole TS, Jones LKR, McGrogan P, Pearce MS, Flood TJ, Cant AJ, Goldblatt D, Thrasher AJ, Gennery AR, McKendrick F, Titman P. Emotional and behavioural difficulties in chronic granulomatous disease. Archives of Disease in Childhood 2012, 97(1), 87-87.
  • Elemraid MA, Pollard K, Thomas MF, Gennery AR, Eastham KM, Rushton SP, Hampton F, Singleton P, Gorton R, Spencer DA, Clark JE, NE England Paediatric Resp Infect. Validity of using Hospital Episode Statistics data on monitoring disease trends. Thorax 2011, 66(9), 827.
  • Slatter MA, Angus B, Windebank K, Taylor A, Meaney C, Lester T, Norbury G, Hambleton S, Abinun M, Flood TJ, Cant AJ, Gennery AR. Polymorphous lymphoproliferative disorder with Hodgkin-like features in common gamma-chain-deficient severe combined immunodeficiency. Journal of Allergy and Clinical Immunology 2011, 127(2), 533-535.
  • Moss SJ, Fenton AC, Gennery AR. Use of conjugate pneumococcal vaccine by United Kingdom neonatal intensive care units. Archives of Disease in Childhood, Fetal and Neonatal Edition 2005, 90(2), 187-188.
  • Dawson C, Slatter MA, Gennery AR. In utero transplantation: baby steps towards an effective therapy. Bone Marrow Transplantation 2005, 36(6), 563-564.
  • Gennery AR, Slatter MA, Bhattacharya A, Jeggo PA, Abinun M, Flood TJ, Cant AJ. Bone marrow transplantation for Nijmegan breakage syndrome. Journal of Pediatric Hematology/Oncology 2005, 27(4), 239.
  • Lakshman R, Gennery AR, Arkwright PD, Flood T, Abinun M, Spickett G, Borrows R, Cant AJ, Balmer P, Borrow R. Assessing immune responses to pneumococcal vaccines. Archives of Disease in Childhood 2003, 88(7), 648-649.
  • Kearns AM, Turner AJL, Taylor CE, George PW, Freeman R, Gennery AR. LightCycler-based quantitative PCR for rapid detection of human herpesvirus 6 DNA in clinical material. Journal of Clinical Microbiology 2001, 39(8), 3020-3021.
  • Datta HK, Cook DB, Kanan RM, Gennery AR, Cant AJ. Evidence for continuous basal generation of Gc-MAF: Absence in infantile osteopetrosis and restoration after bone marrow transplant. Blood 1999, 93(11), 4026-4027.

• Notes

  • Gale RP, Hinterberger W, Young NS, Gennery AR, Dvorak CC, Hebert KM, Heim M, Broglie L, Eapen M. What causes aplastic anaemia?. Leukemia 2023, 37, 1191-1193.
  • Nightingale R, Cavanagh C, Gennery AR. Evaluation of newborn screening for severe combined immunodeficiency (SCID). British Journal of General Practice 2021, 71(711), 456-457.
  • Gennery AR, Lankester A. Long term outcome and immune function after hematopoietic stem cell transplantation for primary immunodeficiency. Frontiers in Pediatrics 2019, 7, 381.
  • Ghosh S, Drexler I, Bhatia S, Adler H, Gennery AR, Borkhardt A. Erratum: Corrigendum: Interleukin-2-Inducible T-Cell Kinase Deficiency-New Patients, New Insight? (Frontiers in immunology (2018) 9 (979)). Frontiers in Immunology 2018, 9, 2197-2197.
  • Dobbs K, Tabellini G, Calzoni E, Patrizi O, Martinez P, Giliani SC, Moratto D, Al-Herz W, Cancrini C, Cowan M, Bleesing J, Booth C, Buchbinder D, Burns SO, Chatila TA, Chou J, Daza-Cajigal V, de Bruin LMO, de la Morena MT, Di Matteo G, Finocchi A, Geha R, Goyal RK, Hayward A, Holland S, Huang C-H, Kanariou MG, King A, Kaplan B, Kleva A, Kuijpers TW, Lee BW, Lougaris V, Massaad M, Meyts I, Morsheimer M, Neven B, Pai S-Y, Parvaneh N, Plebani A, Prockop S, Reisli I, Soh JY, Somech R, Torgerson TR, Kim Y-J, Walter JE, Gennery AR, Keles S, Manis JP, Marcenaro E, Moretta A, Parolini S, Notarangelo LD. Corrigendum: Natural killer cells from patients with recombinase-activating gene and non-homologous end joining gene defects comprise a higher frequency of CD56bright NKG2A+++ cells, and yet display increased degranulation and higher perforin content [Front Immunol, 8, (2017), (798)] doi: 10.3389/fimmu.2017.00798. Frontiers in Immunology 2017, 8(OCT).
  • Gennery AR, Clark JE, Flood TJ, Cant AJ. T-cell-depleted bone marrow transplantation from unrelated donor for [correction of allogeneic sibling for] X-linked hyperimmunoglobulin M syndrome. Journal of Pediatrics 2000, 137(2), 290-290.

• Reviews

  • Tsilifis C, Slatter MA, Gennery AR. Too much of a good thing: a review of primary immune regulatory disorders. Frontiers in Immunology 2023, 14, 1279201.
  • Slatter MA, Gennery AR. Haematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease. Journal of Clinical Medicine 2023, 12(18), 6083.
  • Bojanic I, Worel N, Pacini CP, Stary G, Piekarska A, Flinn AM, Schell KJ, Gennery AR, Knobler R, Lacerda JF, Greinix HT, Pulanic D, Crossland RE. Extracorporeal photopheresis as an immunomodulatory treatment modality for chronic GvHD and the importance of emerging biomarkers. Frontiers in Immunology 2023, 14, 1086006.
  • Gennery AR, Worth A. Severe combined immunodeficiency: Newborn screening and the BCG vaccination. Archives of Disease in Childhood 2022, 107(10), 955-955.
  • Flinn AM, Gennery AR. Primary immune regulatory disorders: Undiagnosed needles in the haystack?. Orphanet Journal of Rare Diseases 2022, 17(1), 99.
  • Pastorczak A, Attarbaschi A, Bomken S, Borkhardt A, van der Werff ten Bosch J, Elitzur S, Gennery AR, Hlavackova E, Kerekes A, Krenova Z, Mlynarski W, Szczepanski T, Wassenberg T, Loeffen J. Consensus Recommendations for the Clinical Management of Hematological Malignancies in Patients with DNA Double Stranded Break Disorders. Cancers 2022, 14(8), 2000.
  • Slatter MA, Gennery AR. Treosulfan-based conditioning for inborn errors of immunity. Therapeutic Advances in Hematology 2021, 12, 1-19.
  • Cordonnier C, Ljungman P, Cesaro S, Hirsch HH, Maschmeyer G, Von Lilienfeld-Toal M, Vehreschild M, Mikulska M, Emonts M, Gennery AR, Neofytos D, Bochud P-Y, Einsele H, Maertens J. The EHA Research Roadmap: Infections in Hematology. HemaSphere 2021, 5(12), e662-e662.
  • Gennery AR. Progress in treating chronic granulomatous disease. British Journal of Haematology 2021, 192(2), 251-264.
  • Puck JM, Gennery AR. Establishing newborn screening for SCID in the USA; experience in California. International Journal of Neonatal Screening 2021, 7(4), 72.
  • Lankester AC, Albert MH, Booth C, Gennery AR, Gungor T, Honig M, Morris EC, Moshous D, Neven B, Schulz A, Slatter M, Veys P. EBMT/ESID inborn errors working party guidelines for hematopoietic stem cell transplantation for inborn errors of immunity. Bone Marrow Transplantation 2021, 56, 2052-2062.
  • Abd Hamid IJ, Azman NA, Gennery AR, Mangantig E, Hashim IF, Zainudeen ZT. Systematic Review of Primary Immunodeficiency Diseases in Malaysia: 1979–2020. Frontiers in Immunology 2020, 11, 1923.
  • Lum SH, Slatter MA. Malignancy post-hematopoietic stem cell transplant in patients with primary immunodeficiency. Expert Review of Clinical Immunology 2020, 16(5), 493-511.
  • Hurst JR, Warnatz K, Alfaro TM, Baumann U, Bergeron A, Burns SO, Condliffe A, Gennery AR, Haerynck F, Jacob J, Jolles S, Malphettes M, Meignin V, Milota T, Prasse A, Quinti I, Renzoni E, Stolz D, van de Ven AAJM. Interstitial lung disease in primary immunodeficiency: Towards a brighter future. European Respiratory Journal 2020, 55(4), 2000089.
  • Wolska-Kusnierz B, Gennery AR. Hematopoietic Stem Cell Transplantation for DNA Double Strand Breakage Repair Disorders. Frontiers in Pediatrics 2020, 7, 557.
  • Knobler R, Arenberger P, Arun A, Assaf C, Bagot M, Berlin G, Bohbot A, Calzavara-Pinton P, Child F, Cho A, French LE, Gennery AR, Gniadecki R, Gollnick HPM, Guenova E, Jaksch P, Jantschitsch C, Klemke C, Ludvigsson J, Papadavid E, Scarisbrick J, Schwarz T, Stadler R, Wolf P, Zic J, Zouboulis C, Zuckermann A, Greinix H. European dermatology forum – updated guidelines on the use of extracorporeal photopheresis 2020 – part 1. Journal of the European Academy of Dermatology and Venereology 2020, 34(12), 2693-2716.
  • Gennery AR, Albert MH, Slatter MA, Lankester A. Hematopoietic Stem Cell Transplantation for Primary Immunodeficiencies. Frontiers in Pediatrics 2019, 7, 445.
  • Lum SH, Neven B, Slatter MA, Gennery AR. Hematopoietic Cell Transplantation for MHC Class II Deficiency. Frontiers in Pediatrics 2019, 7, 516.
  • Lum SH, Hoenig M, Gennery AR, Slatter MA. Conditioning Regimens for Hematopoietic Cell Transplantation in Primary Immunodeficiency. Current Allergy and Asthma Reports 2019, 19(11), 52.
  • Shillitoe BMJ, Gennery AR. An update on X-Linked agammaglobulinaemia: clinical manifestations and management. Current Opinion in Allergy and Clinical Immunology 2019, 19(6), 571-577.
  • Gennery AR. Predicting the future with TRECs. Blood 2018, 132(17), 1731-1733.
  • Slatter MA, Gennery AR. Hematopoietic cell transplantation in primary immunodeficiency–conventional and emerging indications. Expert Review of Clinical Immunology 2018, 14(2), 103-114.
  • Bomken S, van der Werff Ten Bosch J, Attarbaschi A, Bacon CM, Borkhardt A, Boztug K, Fischer U, Hauck F, Kuiper RP, Lammens T, Loeffen J, Neven B, Pan-Hammarstrom Q, Quinti I, Seidel MG, Warnatz K, Wehr C, Lankester AC, Gennery AR. Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Working Group. Frontiers in Immunology 2018, 9, 2912.
  • Laberko A, Gennery AR. Clinical considerations in the hematopoietic stem cell transplant management of primary immunodeficiencies. Expert Review of Clinical Immunology 2018, 14(4), 297-306.
  • Flinn AM, Gennery AR. Adenosine deaminase deficiency: A review. Orphanet Journal of Rare Diseases 2018, 13(1), 65.
  • Flinn AM, Gennery AR. Treatment of pediatric acute graft-versus-host disease-lessons from primary immunodeficiency?. Frontiers in Immunology 2017, 8, 328.
  • Slatter MA, Gennery AR. Approaches to the removal of T-lymphocytes to minimize graft-versus-host disease in patients with primary immunodeficiencies who do not have a matched sibling donor. Current Opinion in Allergy and Clinical Immunology 2017, 17(6), 414-420.
  • Flinn AM, Gennery AR. Extracoporeal photopheresis treatment of acute graft-versus-host disease following allogeneic haematopoietic stem cell transplantation [version 1; referees: 2 approved]. F1000Research 2016, 5.
  • Altmann T, Gennery AR. DNA ligase IV syndrome; a review. Orphanet Journal of Rare Diseases 2016, 11, 137.
  • Bigley V, Barge D, Collin M. Dendritic cell analysis in primary immunodeficiency. Current Opinion in Allergy & Clinical Immunology 2016, 16(6), 530-540.
  • Gennery AR, Maggina P. Infection following haematopoietic stem cell transplantation. Paediatrics and Child Health 2014, 24(6), 236-241.
  • Gennery AR. Immunological features of 22q11 deletion syndrome. Current Opinion in Pediatrics 2013, 25(6), 730-735.
  • Battersby AC, Cale CM, Goldblatt D, Gennery AR. Clinical Manifestations of Disease in X-Linked Carriers of Chronic Granulomatous Disease. Journal of Clinical Immunology 2013, 33(8), 1276-1284.
  • Slatter MA, Gennery AR. Advances in hematopoietic stem cell transplantation for primary immunodeficiency. Expert Review of Clinical Immunology 2013, 9(10), 991-999.
  • Weinacht KG, Brauer PM, Felgentreff K, Devine A, Gennery AR, Giliani S, Al-Here W, Schambach A, Zuniga-Pflucker JC, Notarangelo LD. The role of induced pluripotent stem cells in research and therapy of primary immunodeficiencies. Current Opinion in Immunology 2012, 24(5), 617-624.
  • Gennery AR. Immunological aspects of 22q11.2 deletion syndrome. Cellular and Molecular Life Sciences 2012, 69(1), 17-27.
  • van der Burg M, Gennery AR. Educational paper: The expanding clinical and immunological spectrum of severe combined immunodeficiency. European Journal of Pediatrics 2011, 170(5), 561-571.
  • Slatter MA, Gennery AR. Primary immunodeficiencies associated with DNA-repair disorders. Expert Reviews in Molecular Medicine 2010, 12, e9.
  • Abinun M, Flood TJ, Cant AJ, Veys P, Gennery AR, Foster HE, Friswell M, Baildam E, Davidson J, Southwood TR, Livermore P, Wedderburn LR. Autologous T cell depleted haematopoietic stem cell transplantation in children with severe juvenile idiopathic arthritis in the UK (2000-2007). Molecular Immunology 2009, 47(1), 46-51.
  • Slatter MA, Gennery AR. Clinical Immunology Review Series: An approach to the patient with recurrent infections in childhood. Clinical and Experimental Immunology 2008, 152(3), 389-396.
  • McLean-Tooke A, Spickett GP, Gennery AR. Immunodeficiency and Autoimmunity in DiGeorge syndrome. Scandinavian Journal of Immunology 2007, 66(1), 1-7.
  • McLean-Tooke A, Spickett GP, Gennery AR. Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome. Scandinavian Journal of Immunology 2007, 66(1), 1-7.
  • Gennery AR, Cant AJ. Cord blood stem cell transplantation in primary immune deficiencies. Current Opinion in Allergy and Clinical Immunology 2007, 7(6), 528-534.
  • Slatter MA, Gennery AR. Umbilical cord stem cell transplantation for primary immunodeficiencies. Expert Opinion on Biological Therapy 2006, 6(6), 555-565.
  • Gennery AR, Cant AJ. The immunocompromised host: The patient with recurrent infection. Advances in Experimental Medicine and Biology 2004, 549, 109-117.
  • O'Driscoll M, Gennery AR, Seidel J, Concannon P, Jeggo PA. An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome. DNA Repair 2004, 3(8-9), 1227-1235.
  • Gennery AR, Cant AJ, Jeggo PA. Immunodeficiency associated with DNA repair defects. Clinical and Experimental Immunology 2000, 121(1), 1-7.