Andrew M Will
Overview
Explore the profile of Andrew M Will including associated specialties, affiliations and a list of published articles.
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17
Citations
195
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Recent Articles
1.
Ellingford J, Telford N, Urquhart J, Will A, Bonney D, Adams B, et al.
Cancer Genet
. 2021 May;
256-257:77-80.
PMID: 33957466
Pathogenic germ-line variants in GATA2 (GATA2-deficiency) can cause childhood myelodysplastic syndrome (MDS) and acute myeloid leukaemia (AML), and can be associated with distinct clinical syndromic features. However, penetrance and genotype-phenotype...
2.
Grainger J, Thachil J, Will A
Br J Haematol
. 2018 Aug;
182(5):621-632.
PMID: 30117143
The inherited platelet glycoprotein deficiencies, Glanzmann thrombasthenia (GT) and Bernard Soulier syndrome (BSS) are rare but important long-term bleeding disorders. Once diagnosed, affected patients should be referred to a specialist...
3.
Stivaros S, Alston R, Wright N, Chandler K, Bonney D, Wynn R, et al.
Br J Radiol
. 2015 Sep;
88(1056):20150088.
PMID: 26369989
Objective: Fanconi anaemia (FA) is an inherited disease associated with congenital and developmental abnormalities resulting from the disruption of a multigenic DNA damage response pathway. This study aimed to define...
4.
Smetsers S, Muter J, Bristow C, Patel L, Chandler K, Bonney D, et al.
Fam Cancer
. 2012 Jul;
11(4):661-5.
PMID: 22829014
Fanconi anaemia (FA) is an inherited disease with congenital and developmental abnormalities characterised by cellular cross linker hypersensitivity. FA is caused by mutations in any of so far 15 identified...
5.
Sutherland M, Cumming A, Bowman M, Bolton-Maggs P, Bowen D, Collins P, et al.
Blood
. 2009 Apr;
114(5):1091-8.
PMID: 19372260
Direct sequencing of VWF genomic DNA in 21 patients with type 3 von Willebrand disease (VWD) failed to reveal a causative homozygous or compound heterozygous VWF genotype in 5 cases....
6.
Meyer S, Fergusson W, Whetton A, Moreira-Leite F, Pepper S, Miller C, et al.
Genes Chromosomes Cancer
. 2007 Jan;
46(4):359-72.
PMID: 17243162
Fanconi anemia (FA) is an inherited disease with congenital abnormalities and an extreme risk of acute myeloid leukemia (AML). Genetic events occurring during malignant transformation in FA and the biology...
7.
Meyer S, Eden T, Brennan B, Stevens R, Makin G, Wynn R, et al.
Br J Haematol
. 2006 Jul;
134(2):244-5.
PMID: 16846487
No abstract available.
8.
Meyer S, Barber L, White D, Will A, Birch J, Kohler J, et al.
Br J Haematol
. 2006 Apr;
133(3):284-92.
PMID: 16643430
Childhood acute myeloid leukaemia (AML) is uncommon. Children with Fanconi anaemia (FA), however, have a very high risk of developing AML. FA is a rare inherited disease caused by mutations...
9.
Greenfield H, Gharib M, Turner A, Guiver M, Carr T, Will A, et al.
Pediatr Blood Cancer
. 2005 Oct;
47(2):200-5.
PMID: 16206207
Background: Epstein-Barr virus (EBV) associated lymphoproliferative disease is a complication of haemopoietic stem cell transplantation (HSCT). In certain groups (unrelated and mismatched donor transplants, T-cell depleted) the risk may be...
10.
Barber L, Barlow R, Meyer S, White D, Will A, Eden T, et al.
Br J Haematol
. 2005 Aug;
130(5):796-7.
PMID: 16115142
No abstract available.