Upal Hossain
Overview
Explore the profile of Upal Hossain including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
259
Followers
0
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Recent Articles
1.
Tummala H, Walne A, Badat M, Patel M, Walne A, Alnajar J, et al.
EMBO Mol Med
. 2024 Aug;
16(10):2560-2582.
PMID: 39198715
Dyskeratosis congenita (DC) is a rare inherited bone marrow failure syndrome, caused by genetic mutations that principally affect telomere biology. Approximately 35% of cases remain uncharacterised at the genetic level....
2.
Rio-Machin A, Vulliamy T, Hug N, Walne A, Tawana K, Cardoso S, et al.
Nat Commun
. 2020 Feb;
11(1):1044.
PMID: 32098966
The inclusion of familial myeloid malignancies as a separate disease entity in the revised WHO classification has renewed efforts to improve the recognition and management of this group of at...
3.
Chanchlani N, Rack D, Hossain U, Leigh A
Arch Dis Child Educ Pract Ed
. 2019 Jun;
106(1):35-37.
PMID: 31167853
No abstract available.
4.
Tahmasebi F, Hussain K, Smart G, Gupta M, Hossain U
Obstet Med
. 2017 Dec;
10(4):189-191.
PMID: 29225681
An asymptomatic 36-year-old woman presented with significantly elevated white blood cells (165.9 × 10/L) at antenatal booking, in her first pregnancy. Further investigations revealed the diagnosis of chronic lymphocytic leukaemia...
5.
Chanchlani N, Harewood C, Hossain U, Leigh A
J Pediatr Hematol Oncol
. 2015 Jul;
37(7):574-5.
PMID: 26207774
No abstract available.
6.
Tummala H, Kirwan M, Walne A, Hossain U, Jackson N, Pondarre C, et al.
Am J Hum Genet
. 2014 Feb;
94(2):246-56.
PMID: 24507776
Exome sequencing was performed in three index cases with bone marrow failure and neurological dysfunction and whose parents are first-degree cousins. Homozygous truncating mutations were identified in ERCC6L2 in two...
7.
Kirwan M, Walne A, Plagnol V, Velangi M, Ho A, Hossain U, et al.
Am J Hum Genet
. 2012 May;
90(5):888-92.
PMID: 22541560
Aplastic anemia (AA) and myelodysplasia (MDS) are forms of bone marrow failure that are often part of the same progressive underlying disorder. While most cases are simplex and idiopathic, some...
8.
Holme H, Hossain U, Kirwan M, Walne A, Vulliamy T, Dokal I
Br J Haematol
. 2012 Apr;
158(2):242-248.
PMID: 22533337
The myelodysplastic syndromes (MDS) are heterogeneous and can evolve into acute myeloid leukaemia (AML). Rare familial cases are reported in which five disease genes have been identified to date (RUNX1,...
9.
Vulliamy T, Kirwan M, Beswick R, Hossain U, Baqai C, Ratcliffe A, et al.
PLoS One
. 2011 Sep;
6(9):e24383.
PMID: 21931702
The bone marrow failure syndrome dyskeratosis congenita (DC) has been considered to be a disorder of telomere maintenance in which disease features arise due to accelerated shortening of telomeres. By...
10.
Kirwan M, Beswick R, Walne A, Hossain U, Casimir C, Vulliamy T, et al.
Br J Haematol
. 2011 Apr;
153(5):634-43.
PMID: 21477209
Dyskeratosis congenita (DC) is a heterogeneous bone marrow failure disorder with known mutations in components of telomerase and telomere shelterin. Recent work in a mouse model with a dyskerin mutation...