Newcastle University

Roles and Responsibilities

Clinical Reader 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

Research and Development Lead – Child Health

Bio-Bank working party member – University of Newcastle/– Newcastle upon Tyne Hospital Trust

Lecturer in Immunology for CSIM2, CSIM3, MRes Biomolecular Sciences

Qualifications

MD, MRCP, FRCPCH, DCH, Dip Med Sci

Memberships

European Society of Immunodeficiency Genetics Working Party Member

European Society of Immunodeficiency Inborn Errors Working Party Member

European Society of Immunodeficiency

British Society of Immunology

British Paediatric Allergy, Immunology and Infectious Diseases Group

Member of UK Paediatric Vaccine Group

Member of committee compiling international guidelines for the management of patients with 22q11 deletion

Research Interests

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

Other Expertise

Defects in Non homologous end joining and human disease

Current Work

Investigations into VDJ recombination ability in patients with severe immunodeficiency and sensitivity to ionising radiation. We have established a fibroblast assay to measure VDJ recombination in vitro and are looking at VDJ recombination in a family with severe T cell immunodeficiency. We aim to utilise this assay with other patients with impaired VDJ recombination to examine fidelity.

A study to determine whether preterm infants can make a protective antibody response to the pneumococcal serotypes in Prevenar conjugate heptavalent pneumococcal vaccine following the national UK immunisation schedule:

This is a multicentre clinical study with Alan Fenton in Neonatolgy to assess the efficacy of a new conjugated pneumococcal vaccine in pre-term neonates. This has established a multivalent pneumococcal ELISA assay in Newcastle, and will compliment some of the current research into the nature of the pneumococcal antibody response.

An investigation into the basis of polysaccharide antibody deficiency in paediatric patient groups with poor IgG responses to pneumococcal polysaccharide:

An ongoing project to investigate in detail the phenotypic profile of paediatric patients with polysaccharide antibody deficiency.

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.

Assessment of Disease causing RAG mutations in T-B- SCID and Omenn Syndrome:

This project is looking at whether differences in RAG gene mutations can explain the different clinical presentations of RAG deficient Omenn Syndrome, combined immunodeficiency and RAG deficient T-B- SCID. Currently, 1 MSc student working with me and Dr Pete Middleton (Academic Heamatology).

Investigating a new human innmunodeficiency related to NEMO defects:

A collaborative project with Jean-Laurent Casanova in Paris to investigate a new human immunodeficiency related to NEMO defects.

Future Research

I am setting up a project to investigate The Role of Regulatory T cells in Thymic Dysregulation and Autoimmunity in DiGeorge Association.

I am establishing a project in collaboration with Anne Dickinson, Xiao Wang,(Academic Haematology) to look at Regulatory T cell function. I am also looking to identify DiGeorge thymus by ultrasound and correlate this with immune function.

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 1 PhD student
Identification of non-HLA gene polymorphisms association with post transplant complications following bone marrow transplantation using a genome -wide scanning methodology. (2006-2009)

I am currently supervising 3 MD students:
The Impact of a Conjugate Pneumcoccal Vaccine (Prevenar) on the Epidemiology and Aetiology of Childhood Pneumonia in the North East (2009-2011)

Antibody avidity in preterm infants (2008-2010)

Enhanced surveillance of pneumococcal empyema (2007-2009)

I have successfully supervised the following:

MD student 2006-2008
The Role of Regulatory T cells in Thymic Dysregulation and Autoimmunity in DiGeorge Association. – Awarded February 2009 With Commendation

MD student 2004-2006
A study to determine whether preterm infants can make a protective antibody response to the pneumococcal serotypes in Prevenar conjugate heptavalent pneumococcal vaccine following the national UK immunisation schedule – Awarded December 2007

MRes Student project 1 2006
Do differences in GvHD-associated cytokine polymorphisms account for the development of Omenn’s syndrome rather than T-B- Severe combined immunodeficiency in patients with defects in RAG genes? Distinction

MRes Student project 2 2006
Do differences in GvHD-associated cytokine polymorphisms account for the development of Omenn’s syndrome rather than T-B- Severe combined immunodeficiency in patients with defects in RAG genes? Distinction

BMedSci student 2002-2003
In vitro Interferon g (IFN g) production as an aid in the diagnosis of mycobacterial infection and illness, including tuberculosis, in children.

MSc Student project 2008
Assessment of Disease causing RAG mutations in T-B- SCID and Omenn Syndrome - Pass

MSc Student project 2006
Autozygosity mapping of chromosome 7 region - Search for a New Gene Causing Omenn’s Syndrome variant of T Cell Negative Severe Combined immunodeficiency - Merit

Esteem Indicators

I am a member of the UK Paediatric Vaccine Group. I have spoken at parent’s days for 4 national charities; The Bubble Foundation UK, The Chronic Granulomatous Disease Research Trust, Max Appeal and the Velocardiofacial Syndrome charity. I am an editorial board member of the Open Transplant Journal. I have regularly reviewed articles for national and international journals. I have reviewed grant proposals. I have been a specialist advisor to the Gene Therapy Advisor Committee in 2005 and 2007. I am research and development lead for Child Health and a member of the Clinical Research Centre Executive Board. I am the Designated Individual of the Therapeutic Human Tissue Banks for the Newcastle upon Tyne NHS Foundation Trust.

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

• 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.
• Tilgner K, Neganova I, Moreno I, AlAama 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. In Press.
• Maggina P, Gennery AR. Classification of primary immunodeficiencies: Need for a revised approach?. Journal of Allergy and Clinical Immunology 2013, 131(2), 292-294.
• 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.
• 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.
• 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. The Journal of Experimental Medicine 2012, 209(2), 291-305.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• Cole T, McKendrick F, Titman P, Cant AJ, Pearce MS, Cale CM, Goldblatt D, Gennery AR. Quality of life and emotional funcitoning in children with chronic granulomatous disease. 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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, 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• Slatter MA, Gennery AR. Primary immunodeficiencies associated with DNA-repair disorders. Expert Reviews in Molecular Medicine 2010, 12, e9.
• Slatter MA, Gennery AR. Primary Immunodeficiency Syndromes. In: Diseases of DNA repair. Berlin, Germany: Springer, 2010, pp.146-165.
• 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.
• 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.
• 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.
• 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.
• 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.e11.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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).
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.e4.
• 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.e4.
• 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.
• Du L, van der Burg M, Popov SW, Kotnis A, van Dongen JJM, Gennery AR, Pan-Hammarström Q. Involvement of Artemis in non-homologous end-joining during immunoglobulin class switch recombination. Journal of Experimental Medicine 2008, 205(13), 3031-3040.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• McLean-Tooke A, Spickett GP, Gennery AR. Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome. Scandinavian Journal of Immunology 2007, 66(1), 1-7.
• McLean-Tooke A, Spickett GP, Gennery AR. Immunodeficiency and Autoimmunity in DiGeorge syndrome. Scandinavian Journal of Immunology 2007, 66(1), 1-7.
• 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, 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).
• 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.
• Larmouth W, Galloway A, Taylor C, Slatter M, Gennery A. Protective isolation - an argument in favour. Bone Marrow Transplantation 2007, 39, S250-S251.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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. Primary immunodeficiency syndromes associated with defective DNA double-strand break repair. British Medical Bulletin 2006, 77-78, 71-85.
• 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.
• Slatter MA, Gennery AR. Umbilical cord stem cell transplantation for primary immunodeficiencies. Expert Opinion on Biological Therapy 2006, 6(6), 555-565.
• 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.
• 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 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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, 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.
• 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.
• 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.
• 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.
• 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. 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• Gennery AR, Thrasher A. Gene therapy for severe combined immunodeficiency. Current Anaesthesia and Critical Care 2004, 15(1), 3-9.
• Gennery AR, Spencer DA, Cant AJ. Immune Deficiency and the Lung. Current Paediatrics 2004, 14(2), 115-121.
• 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.
• 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.
• 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, Cant AJ. The immunocompromised host: The patient with recurrent infection. Advances in Experimental Medicine and Biology 2004, 549, 109-117.
• 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.
• 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.
• 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, 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• Gennery AR, O'Driscoll M. Unravelling the web of DNA repair disorders. Clinical and Experimental Immunology 2003, 134(3), 385-387.
• 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.
• 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, Cant AJ. Development of allergy post-bone marrow transplantation. Clinical and Experimental Allergy 2002, 32(12), 1677-1678.
• Gennery AR, Cant AJ. Applied Physiology: Immune Competence. Current Paediatrics 2001, 11(6), 458-464.
• 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, 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.
• 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, 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, Cant AJ. Diagnosis of severe combined immunodeficiency. Journal of Clinical Pathology 2001, 54(3), 191-195.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• Gennery AR, Cant AJ, Jeggo PA. Immunodeficiency associated with DNA repair defects. Clinical and Experimental Immunology 2000, 121(1), 1-7.
• 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.
• 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, 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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, Bartlett K, Hasan A. Thiamine deficiency mimicking acute rejection following cardiac transplantation. Cardiology in the Young 1998, 8(1), 113-115.