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Kiran Tawana

Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma
2013 · Jessica Okosun, Csaba Bödör, et al. · Nature Genetics · 734
Disease evolution and outcomes in familial AML with germline CEBPA mutations
2015 · Kiran Tawana, Jun Wang, et al. · Blood · 201
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants
2020 · Ana Rio-Machin, Tom Vulliamy, et al. · Nature Communications · 113
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Familial CEBPA-mutated acute myeloid leukemia
2017 · Kiran Tawana, Ana Rio-Machin, et al. · Seminars in Hematology · 64
GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML
2018 · Ahad F. Al Seraihi, Ana Rio-Machin, et al. · Leukemia · 59
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Universal genetic testing for inherited susceptibility in children and adults with myelodysplastic syndrome and acute myeloid leukemia: are we there yet?
2018 · Kiran Tawana, Michael W. Drazer, et al. · Leukemia · 53
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy
2021 · Claire C. Homan, Sarah L. King-Smith, et al. · Haematologica · 52
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GATA 2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations
2013 · Claire L. Green, Kiran Tawana, et al. · British Journal of Haematology · 52
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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 PCR
2013 · Susanna Akiki, Sara A. Dyer, et al. · Genes Chromosomes and Cancer · 48
Integrating germline variant assessment into routine clinical practice for myelodysplastic syndrome and acute myeloid leukaemia: current strategies and challenges
2021 · Kiran Tawana, Anna L. Brown, et al. · British Journal of Haematology · 42
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1 , GATA2 , and DDX41
2023 · Claire C. Homan, Michael W. Drazer, et al. · Blood Advances · 41
Highly variable clinical manifestations in a large family with a novel GATA2 mutation
2013 · P G N J Mutsaers, A A van de Loosdrecht, et al. · Leukemia · 30
Inherited DDX41 mutations: 11 genes and counting
2016 · Kiran Tawana, Jude Fitzgibbon · Blood · 23
Association of unbalanced translocation der(1;7) with germline GATA2 mutations
2021 · Emilia J. Kozyra, Gudrun Göhring, et al. · Blood · 22
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Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree
2017 · Kiran Tawana, Jun Wang, et al. · European Journal of Human Genetics · 14
Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy)
2025 · Martijn P. T. Ernst, Jurjen Versluis, et al. · HemaSphere · 13
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Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies
2016 · Tim Ripperger, Kiran Tawana, et al. · European Journal of Human Genetics · 9
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Characteristics and outcomes of patients with acute promyelocytic leukemia and extreme hyperleukocytosis at presentation
2022 · Harry J. Iland, Nigel Russell, et al. · Blood Advances · 7
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CEBPA-Associated Familial Acute Myeloid Leukemia (AML)
2016 · Kiran Tawana, Jude Fitzgibbon · University of Washington, Seattle eBooks · 7
Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2 and DDX41
2022 · Anna L. Brown, Claire Homan, et al. · Blood · 6
Inherited predisposition to MDS/AML
2018 · Ana Rio Machin, Kiran Tawana, et al. · HemaSphere · 1
Variable Penetrance Is Linked with Monoallelic Gene Expression in Inherited GATA2-Mutated MDS/AML
2016 · Ahad Al Seraihi, Ana Rio-Machin, et al. · Blood · 1
Timing is everything: outcomes of allogeneic HSCT in adults with inborn errors of immunity
2026 · Katharine Orf, Hannah Al Yousuf, et al. · Bone Marrow Transplantation
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Genomics and Diagnostics in Acute Myeloid Leukaemia
2019 · Ahad F. Al Seraihi, Ana Rio-Machin, et al. · Royal Society of Chemistry eBooks
Development of a Data Portal for Aggregation and Analysis of Genomics Data in Familial Platelet Disorder with Predisposition to Myeloid Malignancy - the RUNX1.DB
2018 · Anna L. Brown, Mark Armstrong, et al. · Blood
Works count: 31
Citation count: 1,592
H-index: 14
I10-index: 16
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