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Ahad Al Seraihi, PhD
Ahad Al Seraihi, PhD
The Saudi Ministry of Health; Barts Cancer Institute, Queen Mary University of London
Verified email at qmul.ac.uk
Title
Cited by
Cited by
Year
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma
J Okosun, RL Wolfson, J Wang, S Araf, L Wilkins, BM Castellano, ...
Nature genetics 48 (2), 183-188, 2016
2362016
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants
A Rio-Machin, T Vulliamy, N Hug, A Walne, K Tawana, S Cardoso, ...
Nature communications 11 (1), 1044, 2020
932020
Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia
SR Cardoso, G Ryan, AJ Walne, A Ellison, R Lowe, H Tummala, ...
Leukemia 30 (10), 2083-2086, 2016
712016
GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML
AF Al Seraihi, A Rio-Machin, K Tawana, C Bödör, J Wang, A Nagano, ...
Leukemia 32 (11), 2502-2507, 2018
682018
Genome instability is a consequence of transcription deficiency in patients with bone marrow failure harboring biallelic ERCC6L2 variants
H Tummala, AD Dokal, A Walne, A Ellison, S Cardoso, ...
Proceedings of the National Academy of Sciences 115 (30), 7777-7782, 2018
412018
KDM5 inhibition offers a novel therapeutic strategy for the treatment of KMT2D mutant lymphomas
J Heward, L Koniali, A D’Avola, K Close, A Yeomans, M Philpott, ...
Blood, The Journal of the American Society of Hematology 138 (5), 370-381, 2021
392021
SARS-CoV-2 Reinfection Rate and Outcomes in Saudi Arabia: A National Retrospective Study
M Al-Otaiby, I Krissaane, A Al Seraihi, J Alshenaifi, MH Qahtani, T Aljeri, ...
International Journal of Infectious Diseases, 2022
212022
Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree
K Tawana, J Wang, PA Király, K Kállay, G Benyó, M Zombori, J Csomor, ...
European Journal of Human Genetics 25 (8), 1020-1024, 2017
202017
Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies
SR Cardoso, ACM Ellison, AJ Walne, D Cassiman, M Raghavan, ...
Haematologica 102 (8), e293, 2017
202017
Demographic Characteristics, Comorbidities, and Length Of Stay of COVID-19 Patients Admitted into Intensive Care Units in Saudi Arabia: A Nationwide Retrospective Study
M Al-Otaiby, K Almutairi, J Vinluan, A Al Seraihi, WB Alonazi, MH Qahtani, ...
Frontiers in Medicine, 1992, 2022
182022
Pattern of self-reported adverse events related to COVID-19 vaccines in Saudi Arabia: A nationwide study
JM Alkhalifah, A Al Seraihi, JA Al-Tawfiq, BF Alshehri, AH Alhaluli, ...
Frontiers in public health 11, 1043696, 2023
62023
The Genetics of Familial Leukaemia and Myelodysplasia
A Al Seraihi
Queen Mary University of London, 2019
12019
Variable Penetrance Is Linked with Monoallelic Gene Expression in Inherited GATA2-Mutated MDS/AML
A Al Seraihi, A Rio-Machin, K Tawana, C Bödör, S Araf, JA Heward, ...
Blood 128 (22), 3916, 2016
12016
Familial emberger syndrome with autoimmunity, hyper-immunoglobulin E and lymphatic impairment caused by a novel GATA2 mutation
M AlGassim, AF Al Seraihi, AF AlShaibani, W Conca, S AlShehri, ...
Hematology/Oncology and Stem Cell Therapy 15 (2), 10, 2022
2022
Genomics and Diagnostics in Acute Myeloid Leukaemia
AF Al Seraihi, A Rio-Machin, K Tawana, S Charrot, D Di Bella, C Bödör, ...
2019
Myelodysplasia and liver disease extend the spectrum of RTEL1
N Pontikos, H Tummala, T Vulliamy, I Rodriguez-Vigil, B Dobbels, ...
2017
WHOLE EXOME SEQUENCING REVEALS NOVEL CANDIDATE GENES IN FAMILIAL MDS/AML
A Rio-Machin, S Cardoso, K Tawana, J Wang, C Chelala, V Plagnol, ...
HAEMATOLOGICA 101, 205-206, 2016
2016
Germline heterozygous DDX41 variants account for a subset of familial myelodysplasia and acute myeloid leukaemia
S Cardoso, G Ryan, A Walne, H Tummala, A Rio-Machin, A Ellison, ...
BRITISH JOURNAL OF HAEMATOLOGY 173, 121-121, 2016
2016
Pattern of self-reported adverse events related to COVID-vaccines in Saudi Arabia: A nationwide study
FU Khan, O Sandulescu, M Al-Otaiby, JM Alkhalifah, JM Alkhalifah, ...
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