Papers matching “chromosomal abnormalities” 74
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Complex karyotype but not other cytogenetic abnormalities is associated with worse posttransplant survival of patients with nucleophosmin 1‐mutated acute myeloid leukemia: A study from the European Society for Blood and Marrow Transplantation Acute Leukemia Working Party
Nour M. Moukalled, Myriam Labopin, Jurjen Versluis, Gèrard Socié, Didier Blaise, Urpu Salmenniemi, +12 more
7citations -
In uveal melanoma Gα-protein GNA11 mutations convey a shorter disease-specific survival and are more strongly associated with loss of BAP1 and chromosomal alterations than Gα-protein GNAQ mutations
Francesca Piaggio, Michela Croce, Francesco Reggiani, Paola Monti, Cinzia Bernardi, Marianna Ambrosio, +16 more
29citations -
The cumulative effect of cytogenetic abnormalities on the outcomes of myeloma patients with del(17p) undergoing AHSCT in EBMT centres between 2016 and 20222026 British Journal of Haematology article Medicine Multiple Myeloma Research and Treatments Open access
Claire Comerford, Patrick John Hayden, Diderik-Jan Eikema, Linda Köster, Sandra Sauer, Annoek E. C. Broers, +20 more
0citations -
Prognostic value of CPSS cytogenetic risk classification in patients with CMML after allogeneic hematopoietic cell transplantation: a retrospective multicenter study of the Chronic Malignancies Working Party of the EBMT2022 Bone Marrow Transplantation article Medicine Hematopoietic Stem Cell Transplantation Open access
Christian Koenecke, Dirk‐Jan Eikema, Sheree Hazelaar, Thomas A. Schroeder, Victoria T. Potter, Nicolaus Martin Kröger, +19 more
5citations -
P-495 Effectiveness and feasibility of integrating genome-wide non-invasive prenatal testing (GW-NIPT) into standard care for recurrent pregnancy loss: A systematic review and SWOT analysis
Matea Skojo, Lisanne van Prooyen Schuurman, Karin E. M. Diderich, Marieke Joosten, Annemarie G. M. G. J. Mulders, Eileen E. L. O. Lashley, +3 more
0citations -
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study2022 The American Journal of Human Genetics article Medicine Prenatal Screening and Diagnostics Open access
Lisanne van Prooyen Schuurman, Erik A. Sistermans, Diane Van Opstal, Lidewij Henneman, Mireille N. Bekker, Caroline J. Bax, +28 more
98citations -
Defining a Subgroup of Myelodysplastic Syndrome Patients With Very Poor‐Risk Cytogenetics Demonstrating a Relatively More Favorable Outcome After Allogeneic Hematopoietic Cell Transplantation
Xavier Poiré, Dirk‐Jan Eikema, Linda Köster, Nicolaus Martin Kröger, Johan A. Maertens, Régis Peffault de Latour, +13 more
0citations