| Adoptive transfer of cytomegalovirus-specific CTL to stem cell transplant patients after selection by HLA–peptide tetramers M Cobbold, N Khan, B Pourgheysari, S Tauro, D McDonald, H Osman, ... The Journal of experimental medicine 202 (3), 379-386, 2005 | 625 | 2005 |
| Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) P Ostergaard, MA Simpson, FC Connell, CG Steward, G Brice, ... Nature genetics 43 (10), 929-931, 2011 | 569 | 2011 |
| Barth syndrome SLN Clarke, A Bowron, IL Gonzalez, SJ Groves, R Newbury-Ecob, ... Orphanet journal of rare diseases 8, 1-17, 2013 | 349 | 2013 |
| X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease C Booth, KC Gilmour, P Veys, AR Gennery, MA Slatter, H Chapel, ... Blood, The Journal of the American Society of Hematology 117 (1), 53-62, 2011 | 349 | 2011 |
| Hematopoietic cell transplantation for inherited metabolic diseases: an overview of outcomes and practice guidelines C Peters, CG Steward Bone marrow transplantation 31 (4), 229-239, 2003 | 320 | 2003 |
| Minimal residual disease status before allogeneic bone marrow transplantation is an important determinant of successful outcome for children and adolescents with acute … CJC Knechtli, NJ Goulden, JP Hancock, VLG Grandage, EL Harris, ... Blood, The Journal of the American Society of Hematology 92 (11), 4072-4079, 1998 | 314 | 1998 |
| Outcome and clinical course of 100 patients with adenovirus infection following bone marrow transplantation A Baldwin, H Kingman, M Darville, ABM Foot, D Grier, JM Cornish, ... Bone marrow transplantation 26 (12), 1333-1338, 2000 | 302 | 2000 |
| Minimal residual disease (MRD) status prior to allogeneic stem cell transplantation is a powerful predictor for post-transplant outcome in children with ALL P Bader, J Hancock, H Kreyenberg, NJ Goulden, D Niethammer, A Oakhill, ... Leukemia 16 (9), 1668-1672, 2002 | 236 | 2002 |
| Long-term outcome of haematopoietic stem cell transplantation in autosomal recessive osteopetrosis: an EBMT report GJA Driessen, EJA Gerritsen, A Fischer, A Fasth, WCJ Hop, P Veys, ... Bone marrow transplantation 32 (7), 657-663, 2003 | 226 | 2003 |
| Neurological aspects of osteopetrosis CG Steward Neuropathology and applied neurobiology 29 (2), 87-97, 2003 | 210 | 2003 |
| Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography–mass spectrometry as a diagnostic test for … RH Houtkooper, RJ Rodenburg, C Thiels, H van Lenthe, F Stet, ... Analytical biochemistry 387 (2), 230-237, 2009 | 205 | 2009 |
| Diagnosis of invasive aspergillosis in bone marrow transplant recipients by polymerase chain reaction ECM Williamson, JP Leeming, HM Palmer, CG Steward, D Warnock, ... British journal of haematology 108 (1), 132-139, 2000 | 187 | 2000 |
| Outcome of hematopoietic stem cell transplantation for adenosine deaminase–deficient severe combined immunodeficiency A Hassan, C Booth, A Brightwell, Z Allwood, P Veys, K Rao, M Hönig, ... Blood, The Journal of the American Society of Hematology 120 (17), 3615-3624, 2012 | 179 | 2012 |
| Similar outcome of upfront‐unrelated and matched sibling stem cell transplantation in idiopathic paediatric aplastic anaemia. A study on behalf of the UK Paediatric BMT Working … C Dufour, P Veys, E Carraro, N Bhatnagar, M Pillon, R Wynn, B Gibson, ... British journal of haematology 171 (4), 585-594, 2015 | 178 | 2015 |
| The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation R Fuge, JM Bird, A Fraser, D Hart, L Hunt, JM Cornish, N Goulden, ... British journal of haematology 113 (1), 58-64, 2001 | 178 | 2001 |
| Unrelated donor bone marrow transplantation for children with relapsed acute lymphoblastic leukaemia in second complete remission A Oakhill, DH Pamphilon, MN Potter, CG Steward, S Goodman, A Green, ... British Journal of Haematology 94 (3), 574-578, 1996 | 172 | 1996 |
| The Barth Syndrome Registry: distinguishing disease characteristics and growth data from a longitudinal study AE Roberts, C Nixon, CG Steward, K Gauvreau, M Maisenbacher, ... American journal of medical genetics Part A 158 (11), 2726-2732, 2012 | 145 | 2012 |
| Barth syndrome: an X‐linked cause of fetal cardiomyopathy and stillbirth CG Steward, RA Newbury‐Ecob, R Hastings, SF Smithson, ... Prenatal diagnosis 30 (10), 970-976, 2010 | 145 | 2010 |
| Infections in adults undergoing unrelated donor bone marrow transplantation E WILLIAMSON, M MILLAR, C STEWARD, J CORNISH, A FOOT, ... British journal of haematology 104 (3), 560-568, 1999 | 144 | 1999 |
| Bloodspot assay using HPLC–tandem mass spectrometry for detection of Barth syndrome W Kulik, H van Lenthe, FS Stet, RH Houtkooper, H Kemp, JE Stone, ... Clinical chemistry 54 (2), 371-378, 2008 | 142 | 2008 |
