Ahad Al Seraihi, PhD
机构: The Saudi Ministry of Health; Barts Cancer Institute, Queen Mary University of London
每年引用次数
引用次数
引用: 673
H-指数: 10
I10-指数 : 10
出版物: 19
Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies
Shirleny R. Cardoso , Alicia C.M. Ellison , Amanda J. Walne , David Cassiman
Haematologica 102 ( 8)
9
2017
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants
Nikolas Pontikos , Jun Wang , Hemanth Tummala , Ahad Fahad H. Al Seraihi
Nature Communications 11 ( 1) 1044
12
2020
Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia
S R Cardoso , G Ryan , A J Walne , A Ellison
Leukemia 30 ( 10) 2083 -2086
67
2016
WHOLE EXOME SEQUENCING REVEALS NOVEL CANDIDATE GENES IN FAMILIAL MDS/AML
A Rio-Machin , S Cardoso , K Tawana , J Wang
HAEMATOLOGICA 101 205 -206
2016
Pattern of self-reported adverse events related to COVID-vaccines in Saudi Arabia: A nationwide study
Farman Ullah Khan , Oana Sandulescu , Maram Al-Otaiby , Joud Mohammed Alkhalifah
The Genetics of Familial Leukaemia and Myelodysplasia
A Al Seraihi
Queen Mary University of London
1
2019
Genome instability is a consequence of transcription deficiency in patients with bone marrow failure harboring biallelic ERCC6L2 variants.
Hemanth Tummala , Arran D. Dokal , Amanda Walne , Alicia Ellison
Proceedings of the National Academy of Sciences of the United States of America 115 ( 30) 7777 -7782
11
2018
Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree.
Kiran Tawana , Jun Wang , Péter A Király , Krisztián Kállay
European Journal of Human Genetics 25 ( 8) 1020 -1024
6
2017
Variable Penetrance Is Linked with Monoallelic Gene Expression in Inherited GATA2-Mutated MDS/AML
Ahad Al Seraihi , Ana Rio-Machin , Kiran Tawana , Csaba Bödör
Blood 128 ( 22) 3916 -3916
1
2016
SARS-CoV-2 reinfection rate and outcomes in Saudi Arabia: A national retrospective study
Maram Al-Otaiby , Ines Krissaane , Ahad Al Seraihi , Jumanah Alshenaifi
International Journal of Infectious Diseases 122 758 -766
21
2022
Germline heterozygous DDX41 variants account for a subset of familial myelodysplasia and acute myeloid leukaemia
Shirleny Cardoso , Gavin Ryan , Amanda Walne , Hemanth Tummala
BRITISH JOURNAL OF HAEMATOLOGY 173 121 -121
2016
Demographic characteristics, comorbidities, and length of stay of COVID-19 patients admitted into intensive care units in Saudi Arabia: a nationwide retrospective study
Maram Al-Otaiby , Khalid M Almutairi , Jason M Vinluan , Ahad Al Seraihi
Frontiers in Medicine 9 893954 -893954
18
2022
Pattern of self-reported adverse events related to COVID-19 vaccines in Saudi Arabia: A nationwide study
Joud Mohammed Alkhalifah , Ahad Al Seraihi , Jaffar A Al-Tawfiq , Badr Fadhel Alshehri
Frontiers in Public Health 11 1043696 -1043696
8
2023
Myelodysplasia and liver disease extend the spectrum of RTEL1
Nikolas Pontikos , Hemanth Tummala , Tom Vulliamy , Inderjeet Rodriguez-Vigil
2017
KDM5 inhibition offers a novel therapeutic strategy for the treatment of KMT2D mutant lymphomas
James Heward , Lola Koniali , Annalisa D’Avola , Karina Close
bioRxiv
20
2020
GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML.
Ahad F Al Seraihi , Ana Rio-Machin , Kiran Tawana , Csaba Bödör
Leukemia 32 ( 11) 2502 -2507
22
2018
Genomics and Diagnostics in Acute Myeloid Leukaemia
Ahad F Al Seraihi , Ana Rio-Machin , Kiran Tawana , Sarah Charrot
2019
Familial emberger syndrome with autoimmunity, hyper-immunoglobulin E and lymphatic impairment caused by a novel GATA2 mutation
Moneerah AlGassim , Ahad F Al Seraihi , AlFadel AlShaibani , Walter Conca
Hematology/Oncology and Stem Cell Therapy 15 ( 2) 63 -65
2022
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma
Jessica Okosun , Rachel L Wolfson , Jun Wang , Shamzah Araf
Nature Genetics 48 ( 2) 183 -188
96
2016