| Megakaryocytes regulate hematopoietic stem cell quiescence via CXCL4 secretion I Bruns, D Lucas, S Pinho, J Ahmed, M Lambert, Y Kunisaki, ... Experimental Hematology 42 (8), S18, 2014 | 658* | 2014 |
| Megakaryocytes regulate hematopoietic stem cell quiescence through CXCL4 secretion I Bruns, D Lucas, S Pinho, J Ahmed, MP Lambert, Y Kunisaki, ... Nature medicine 20 (11), 1315, 2014 | 657 | 2014 |
| Clinical updates in adult immune thrombocytopenia MP Lambert, TB Gernsheimer Blood 129 (21), 2829-2835, 2017 | 467 | 2017 |
| Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ... The American Journal of Human Genetics 100 (1), 75-90, 2017 | 427 | 2017 |
| Sirolimus is effective in relapsed/refractory autoimmune cytopenias: results of a prospective multi-institutional trial KL Bride, T Vincent, K Smith-Whitley, MP Lambert, JJ Bleesing, AE Seif, ... Blood 127 (1), 17-28, 2016 | 211 | 2016 |
| Eltrombopag for the treatment of children with persistent and chronic immune thrombocytopenia (PETIT): a randomised, multicentre, placebo-controlled study JB Bussel, PG De Miguel, JM Despotovic, JD Grainger, J Sevilla, ... The Lancet Haematology 2 (8), e315-e325, 2015 | 211 | 2015 |
| A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders I Simeoni, JC Stephens, F Hu, SVV Deevi, K Megy, TK Bariana, ... Blood, blood-2015-12-688267, 2016 | 193 | 2016 |
| Clinical sequencing exploratory research consortium: accelerating evidence-based practice of genomic medicine RC Green, KAB Goddard, GP Jarvik, LM Amendola, PS Appelbaum, ... The American Journal of Human Genetics 98 (6), 1051-1066, 2016 | 170 | 2016 |
| A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss S Stritt, P Nurden, E Turro, D Greene, SB Jansen, SK Westbury, ... Blood, blood-2015-10-675629, 2016 | 153 | 2016 |
| Neutrophil accumulation and NET release contribute to thrombosis in HIT K Gollomp, M Kim, I Johnston, V Hayes, J Welsh, GM Arepally, M Kahn, ... JCI insight 3 (18), 2018 | 149 | 2018 |
| What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia IM Campbell, SE Sheppard, TB Crowley, DE McGinn, A Bailey, ... American Journal of Medical Genetics Part A 176 (10), 2058-2069, 2018 | 147 | 2018 |
| Platelet factor 4 is a negative autocrine in vivo regulator of megakaryopoiesis: clinical and therapeutic implications MP Lambert, L Rauova, M Bailey, MC Sola-Visner, MA Kowalska, ... Blood 110 (4), 1153-1160, 2007 | 141 | 2007 |
| Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders SK Westbury, E Turro, D Greene, C Lentaigne, AM Kelly, TK Bariana, ... Genome medicine 7 (1), 36, 2015 | 139 | 2015 |
| Hypomorphic CARD11 mutations associated with diverse immunologic phenotypes with or without atopic disease. B Dorjbal, JR Stinson, CA Ma, MA Weinreich, B Miraghazadeh, ... The Journal of Allergy and Clinical Immunology, 2018 | 138* | 2018 |
| Challenges and promises for the development of donor-independent platelet transfusions MP Lambert, SK Sullivan, R Fuentes, DL French, M Poncz Blood 121 (17), 3319-3324, 2013 | 123 | 2013 |
| Bleeding risk of surgery and its prevention in patients with inherited platelet disorders. The Surgery in Platelet disorders And Therapeutic Approach (SPATA) study. S Orsini, P Noris, L Bury, PG Heller, C Santoro, RA Kadir, NC Butta, ... haematologica, haematol. 2016.160754, 2017 | 122 | 2017 |
| defects in Trpm7 channel function deregulate thrombopoiesis through altered cellular Mg2+ homeostasis and cytoskeletal architecture: pp02 S Stritt, P Nurden, R Favier, M Favier, S Ferioli, KS Gotru, JM van Eeuwijk, ... Journal of Thrombosis and Haemostasis 14, 107, 2016 | 117 | 2016 |
| Defects in TRPM7 channel function deregulate thrombopoiesis through altered cellular Mg2+ homeostasis and cytoskeletal architecture S Stritt, P Nurden, R Favier, M Favier, S Ferioli, SK Gotru, ... Nature communications 7, 11097, 2016 | 116 | 2016 |
| A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies E Turro, D Greene, A Wijgaerts, C Thys, C Lentaigne, TK Bariana, ... Science translational medicine 8 (328), 328ra30-328ra30, 2016 | 112 | 2016 |
| Diagnosis and management of autoimmune cytopenias in childhood DT Teachey, MP Lambert Pediatric Clinics 60 (6), 1489-1511, 2013 | 105 | 2013 |
