Publications: Miss Ahad Al Seraihi
Al Seraihi AF, Rio-Machin A, Tawana K, Bödör C, Wang J, Nagano A, Heward JA, Iqbal S et al.(2018).
GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML. Leukemia
vol. 32,
(11)
2502-2507.
Cardoso SR, Ellison ACM, Walne AJ, Cassiman D, Raghavan M, Kishore B, Ancliff P, Rodríguez-Vigil C et al.(2017).
Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies. Haematologica
vol. 102,
(8)
e293-e296.
Tawana K, Wang J, Király PA, Kállay K, Benyó G, Zombori M, Csomor J, Al Seraihi A et al.(2017).
Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree. Eur J Hum Genet
vol. 25,
(8)
1020-1024.
Al Seraihi A, Rio-Machin A, Tawana K, Boedoer C, Araf S, Heward JA, Smith M, Iqbal S et al. (2016).
Variable Penetrance Is Linked with Monoallelic Gene Expression in Inherited GATA2-Mutated MDS/AML. BLOOD.
vol. 128,
Rio-Machin A, Cardoso S, Tawana K, Wang J, Chelala C, Plagnol V, Wallis Y, Ryan G et al. (2016).
WHOLE EXOME SEQUENCING REVEALS NOVEL CANDIDATE GENES IN FAMILIAL MDS/AML. HAEMATOLOGICA.
vol. 101,
205-206.
DOKAL I(2016).
Germline heterozygous DDX41 vriants in a subset of familial myelodysplasia and acute myeloid leukaemia. Leukemia
Okosun J, Wolfson RL, Wang J, Araf S, Wilkins L, Castellano BM, Escudero-Ibarz L, Al Seraihi AF et al. (2016).
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma. Nat Genet.
vol. 48,
183-188.
