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Functional investigation of SLFN14 in megakaryocyte and platelet biology
Morgan, Neil
(Principal Investigator)
Gough, Richard
(Co-Investigator)
Cardiovascular Sciences
Overview
Fingerprint
Research output
(5)
Project Details
Short title
Functional investigation of SLFN14 in megakaryocyte and platelet biology
Status
Finished
Effective start/end date
22/08/17
→
20/02/20
Funding
British Heart Foundation
View all
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Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.
Blood Platelets
Medicine & Life Sciences
100%
Hemorrhage
Medicine & Life Sciences
82%
Genes
Medicine & Life Sciences
57%
Tropomyosin
Medicine & Life Sciences
55%
Exome
Medicine & Life Sciences
51%
Computational Biology
Medicine & Life Sciences
49%
Natural History
Medicine & Life Sciences
42%
Thrombocytopenia
Medicine & Life Sciences
40%
Research output
Research output per year
2020
2020
2021
2022
2022
5
Article
Research output per year
Research output per year
Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases
Vyas, H.
,
Alcheikh, A.
,
Lowe, G.
,
Stevenson, W. S.
,
Morgan, N.
&
Rabbolini, D. J.
,
19 May 2022
, (E-pub ahead of print)
In:
Platelets.
p. 1-6
6 p.
Research output
:
Contribution to journal
›
Article
›
peer-review
Open Access
File
Natural History
100%
Thrombocytopenia
93%
Megakaryocytes
59%
Point Mutation
48%
Thrombocytopenia chromosome breakage
43%
36
Downloads (Pure)
Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression data
UK GAPP Study Group
,
Jan 2021
,
In:
Journal of Thrombosis and Haemostasis.
19
,
1
,
p. 262-268
7 p.
Research output
:
Contribution to journal
›
Article
›
peer-review
Open Access
File
Exome
100%
Blood Platelets
65%
Hemorrhage
53%
Whole Exome Sequencing
43%
Genes
33%
2
Citations (Scopus)
156
Downloads (Pure)
Rare missense variants in Tropomyosin-4 (TPM4) are associated with platelet dysfunction, cytoskeletal defects and excessive bleeding
The UK GAPP Study Group
,
Stapley, R.
,
Poulter, N.
,
Khan, A.
,
Smith, C.
,
Bignell, P.
,
Fratter, C.
,
Lester, W.
,
Lowe, G.
&
Morgan, N.
,
10 Nov 2021
,
In:
Journal of Thrombosis and Haemostasis.
8 p.
Research output
:
Contribution to journal
›
Article
›
peer-review
Open Access
File
Tropomyosin
100%
Blood Platelets
59%
Hemorrhage
49%
Platelet Count
12%
Genes
10%
4
Downloads (Pure)