| Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3) J Feldmann, I Callebaut, G Raposo, S Certain, D Bacq, C Dumont, ... Cell 115 (4), 461-473, 2003 | 1063 | 2003 |
| CATSPER2, a human autosomal nonsyndromic male infertility gene N Avidan, H Tamary, O Dgany, D Cattan, A Pariente, M Thulliez, N Borot, ... European Journal of Human Genetics 11 (7), 497-502, 2003 | 237 | 2003 |
| Rivaroxaban compared with standard anticoagulants for the treatment of acute venous thromboembolism in children: a randomised, controlled, phase 3 trial C Male, AWA Lensing, JS Palumbo, R Kumar, I Nurmeev, K Hege, ... The Lancet Haematology 7 (1), e18-e27, 2020 | 226 | 2020 |
| A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia L Arnaud, C Saison, V Helias, N Lucien, D Steschenko, MC Giarratana, ... The American Journal of Human Genetics 87 (5), 721-727, 2010 | 217 | 2010 |
| Recommendations regarding splenectomy in hereditary hemolytic anemias A Iolascon, I Andolfo, W Barcellini, F Corcione, L Garçon, L De Franceschi, ... haematologica 102 (8), 1304, 2017 | 191 | 2017 |
| Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome A Marrone, A Walne, H Tamary, Y Masunari, M Kirwan, R Beswick, ... Blood, The Journal of the American Society of Hematology 110 (13), 4198-4205, 2007 | 182 | 2007 |
| Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I H Tamary, H Shalev, G Perez-Avraham, M Zoldan, I Levi, DW Swinkels, ... Blood, The Journal of the American Society of Hematology 112 (13), 5241-5244, 2008 | 179 | 2008 |
| Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia … T Kühne, W Berchtold, LA Michaels, R Wu, H Donato, B Espina, H Tamary, ... Haematologica 96 (12), 1831, 2011 | 177 | 2011 |
| Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients S Shalitin, D Carmi, N Weintrob, M Phillip, H Miskin, L Kornreich, R Zilber, ... European journal of haematology 74 (2), 93-100, 2005 | 171 | 2005 |
| How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel PS Rosenberg, H Tamary, BP Alter American journal of medical genetics Part A 155 (8), 1877-1883, 2011 | 167 | 2011 |
| Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1 O Dgany, N Avidan, J Delaunay, T Krasnov, L Shalmon, H Shalev, ... The American Journal of Human Genetics 71 (6), 1467-1474, 2002 | 167 | 2002 |
| Congenital dyserythropoietic anemias: molecular insights and diagnostic approach A Iolascon, H Heimpel, A Wahlin, H Tamary Blood, The Journal of the American Society of Hematology 122 (13), 2162-2166, 2013 | 151 | 2013 |
| Risk factors for central venous catheter thrombotic complications in children and adolescents with cancer S Revel‐Vilk, J Yacobovich, H Tamary, G Goldstein, S Nemet, ... Cancer 116 (17), 4197-4205, 2010 | 141 | 2010 |
| Hepatic iron overload: quantitative MR imaging. JM Gomori, G Horev, H Tamary, J Zandback, L Kornreich, R Zaizov, ... Radiology 179 (2), 367-369, 1991 | 141 | 1991 |
| Bleeding manifestations and management of children with persistent and chronic immune thrombocytopenia: data from the Intercontinental Cooperative ITP Study Group (ICIS) CE Neunert, GR Buchanan, P Imbach, PHB Bolton-Maggs, CM Bennett, ... Blood, The Journal of the American Society of Hematology 121 (22), 4457-4462, 2013 | 122 | 2013 |
| Hypocholesterolemia in chronic anemias with increased erythropoietic activity H Shalev, J Kapelushnik, A Moser, H Knobler, H Tamary American journal of hematology 82 (3), 199-202, 2007 | 114 | 2007 |
| Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation H Heimpel, K Schwarz, M Ebnöther, JS Goede, D Heydrich, T Kamp, ... Blood 107 (1), 334-340, 2006 | 112 | 2006 |
| Paediatric cerebral sinus vein thrombosis G Kenet, D Waldman, A Lubetsky, N Kornbrut, A Khalil, A Koren, ... Thrombosis and haemostasis 92 (10), 713-718, 2004 | 104 | 2004 |
| High incidence of early cholelithiasis detected by ultrasonography in children and young adults with hereditary spherocytosis H Tamary, S Aviner, E Freud, H Miskin, T Krasnov, M Schwarz, I Yaniv Journal of pediatric hematology/oncology 25 (12), 952-954, 2003 | 103 | 2003 |
| The European hematology association roadmap for European hematology research: a consensus document A Engert, C Balduini, A Brand, B Coiffier, C Cordonnier, H Döhner, ... haematologica 101 (2), 115, 2016 | 92 | 2016 |
