| Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes F Thol, S Kade, C Schlarmann, P Löffeld, M Morgan, J Krauter, ... Blood, The Journal of the American Society of Hematology 119 (15), 3578-3584, 2012 | 533 | 2012 |
| STAT3 mutations unify the pathogenesis of chronic lymphoproliferative disorders of NK cells and T-cell large granular lymphocyte leukemia A Jerez, MJ Clemente, H Makishima, H Koskela, F LeBlanc, K Peng Ng, ... Blood, The Journal of the American Society of Hematology 120 (15), 3048-3057, 2012 | 448 | 2012 |
| Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents MW Wlodarski, S Hirabayashi, V Pastor, J Starý, H Hasle, R Masetti, ... Blood, The Journal of the American Society of Hematology 127 (11), 1387-1397, 2016 | 409 | 2016 |
| Mutations in CBL occur frequently in juvenile myelomonocytic leukemia ML Loh, DS Sakai, C Flotho, M Kang, M Fliegauf, S Archambeault, ... Blood, The Journal of the American Society of Hematology 114 (9), 1859-1863, 2009 | 343 | 2009 |
| CD4+CD25high Foxp3+ regulatory T cells in myelodysplastic syndrome (MDS) SY Kordasti, W Ingram, J Hayden, D Darling, L Barber, B Afzali, ... Blood, The Journal of the American Society of Hematology 110 (3), 847-850, 2007 | 314 | 2007 |
| Childhood cancer predisposition syndromes—a concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology T Ripperger, SS Bielack, A Borkhardt, IB Brecht, B Burkhardt, ... American journal of medical genetics Part A 173 (4), 1017-1037, 2017 | 300 | 2017 |
| Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans F Buonocore, P Kühnen, JP Suntharalingham, I Del Valle, M Digweed, ... The Journal of clinical investigation 127 (5), 1700-1713, 2017 | 168 | 2017 |
| GATA2 deficiency and related myeloid neoplasms MW Wlodarski, M Collin, MS Horwitz Seminars in hematology 54 (2), 81-86, 2017 | 162 | 2017 |
| PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia A Stray-Pedersen, PH Backe, HS Sorte, L Mørkrid, NY Chokshi, ... The American Journal of Human Genetics 95 (1), 96-107, 2014 | 159 | 2014 |
| Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study RF Grace, P Bianchi, EJ van Beers, SW Eber, B Glader, HM Yaish, ... Blood, The Journal of the American Society of Hematology 131 (20), 2183-2192, 2018 | 158 | 2018 |
| Pathologic clonal cytotoxic T-cell responses: nonrandom nature of the T-cell–receptor restriction in large granular lymphocyte leukemia MW Wlodarski, C O'Keefe, EC Howe, AM Risitano, A Rodriguez, ... Blood 106 (8), 2769-2780, 2005 | 152 | 2005 |
| Phenotypic differences between healthy effector CTL and leukemic LGL cells support the notion of antigen-triggered clonal transformation in T-LGL leukemia MW Wlodarski, Z Nearman, A Jankowska, N Babel, J Powers, P Leahy, ... Journal of Leucocyte Biology 83 (3), 589-601, 2008 | 141 | 2008 |
| SNP array–based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes MG Afable, M Wlodarski, H Makishima, M Shaik, MA Sekeres, RV Tiu, ... Blood, The Journal of the American Society of Hematology 117 (25), 6876-6884, 2011 | 140 | 2011 |
| Molecular strategies for detection and quantitation of clonal cytotoxic T-cell responses in aplastic anemia and myelodysplastic syndrome MW Wlodarski, LP Gondek, ZP Nearman, M Plasilova, M Kalaycio, ED Hsi, ... Blood 108 (8), 2632-2641, 2006 | 135 | 2006 |
| RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia DB Lipka, T Witte, R Toth, J Yang, M Wiesenfarth, P Nöllke, A Fischer, ... Nature communications 8 (1), 2126, 2017 | 114 | 2017 |
| Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7 VB Pastor, SS Sahoo, J Boklan, GC Schwabe, E Saribeyoglu, B Strahm, ... haematologica 103 (3), 427, 2018 | 109 | 2018 |
| Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes SS Sahoo, VB Pastor, C Goodings, RK Voss, EJ Kozyra, A Szvetnik, ... Nature medicine 27 (10), 1806-1817, 2021 | 105 | 2021 |
| Phosphatidylinositol-3-phosphate kinase pathway activation protects leukemic large granular lymphocytes from undergoing homeostatic apoptosis AE Schade, JJ Powers, MW Wlodarski, JP Maciejewski Blood 107 (12), 4834-4840, 2006 | 101 | 2006 |
| Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9 I Demuth, M Wlodarski, AJ Tipping, NV Morgan, JP de Winter, M Thiel, ... European Journal of Human Genetics 8 (11), 861-868, 2000 | 95 | 2000 |
| Molecular analysis of TCR clonotypes in LGL: a clonal model for polyclonal responses CL O’Keefe, M Plasilova, M Wlodarski, AM Risitano, AR Rodriguez, ... The Journal of Immunology 172 (3), 1960-1969, 2004 | 91 | 2004 |
