U. Hossain

发表

The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants

D. Steinemann, Alison M. Male, J. Fitzgibbon, 2020, Nature Communications.

Long‐haul flights and deep vein thrombosis: a significant risk only when additional factors are also present

A. Cohen, R. Arya, Raj K. Patel, 2002, British journal of haematology.

Dyskeratosis congenita and the DNA damage response

T. Vulliamy, R. Beswick, I. Dokal, 2011, British journal of haematology.

Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia

T. Vulliamy, I. Dokal, A. Walne, 2012, British journal of haematology.

ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function.

V. Plagnol, T. Vulliamy, C. Pondarré, 2014, American journal of human genetics.

Differences in Disease Severity but Similar Telomere Lengths in Genetic Subgroups of Patients with Telomerase and Shelterin Mutations

T. Vulliamy, R. Beswick, I. Dokal, 2011, PloS one.

Telomere length measurement can distinguish pathogenic from non-pathogenic variants in the shelterin component, TIN2

T. Vulliamy, R. Beswick, I. Dokal, 2012, Clinical genetics.

The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants

D. Steinemann, Alison M. Male, J. Fitzgibbon, 2020, Nature Communications.

Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia.

V. Plagnol, T. Vulliamy, I. Dokal, 2012, American journal of human genetics.

Successful pregnancy in the context of previously undiagnosed chronic lymphocytic leukaemia: A case report and literature review

F. Tahmasebi, Manish Gupta, U. Hossain, 2017, Obstetric medicine.