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Leukemia|February 28, 2018
Universal genetic testing for inherited susceptibility in children and adults with myelodysplastic syndrome and acute myeloid leukemia: are we there yet?Kiran Tawana, Michael W Drazer, Jane E ChurpekBritish Journal of Haematology|October 18, 2021
Integrating germline variant assessment into routine clinical practice for myelodysplastic syndrome and acute myeloid leukaemia: current strategies and challengesKiran Tawana, Anna L Brown, Jane E ChurpekSeminars in Hematology|June 23, 2017
Familial CEBPA-mutated acute myeloid leukemiaKiran Tawana, Ana Rio-Machin, Claude Preudhomme, et al.British Journal of Haematology|April 9, 2013
GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutationsClaire L Green, Kiran Tawana, Robert K Hills, et al.Genes, Chromosomes & Cancer|September 4, 2013
NUP98-NSD1 fusion in association with FLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCRSusanna Akiki, Sara A Dyer, David Grimwade, et al.European Journal of Human Genetics : EJHG|May 18, 2017
Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigreeKiran Tawana, Jun Wang, Péter A Király, et al.Nature Genetics|December 24, 2013
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphomaJessica Okosun, Csaba Bödör, Jun Wang, et al.Hemasphere|January 17, 2025
Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy)Martijn P T Ernst, Jurjen Versluis, Peter J M Valk, et al.Blood|July 12, 2015
Disease evolution and outcomes in familial AML with germline CEBPA mutationsKiran Tawana, Jun Wang, Aline Renneville, et al.Nature Communications|February 27, 2020
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variantsAna Rio-Machin, Tom Vulliamy, Nele Hug, et al.Pageof 2