Ben Johnson

发表

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

S. Mundell, M. Simpson, S. Watson, 2016, Haematologica.

Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan

Sarah J. Fletcher, N. Morgan, Ben Johnson, 2016, Platelets.

Molecular genetic investigation into inherited thrombocytopenia

Ben Johnson, 2017 .

University of Birmingham Novel mutations in RASGRP2 encoding for CalDAG-GEFI abrogate Rap1 activation causing platelet dysfunction

David S. Paul, S. Watson, J. Sondek, 2016 .

Utilising the zebrafish model organism to study the effect of FLCN in early embryonic development and Genotyping and platelet phenotyping of cases of rare inherited platelet based bleeding disorders

Ben Johnson, 2013 .

A comprehensive targeted next‐generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia

J. Thachil, M. Williams, N. Morgan, 2018, Research and practice in thrombosis and haemostasis.

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

M. Simpson, S. Watson, M. Lordkipanidzé, 2015, The Journal of clinical investigation.

Novel mutations in RASGRP2, which encodes CalDAG-GEFI, abrogate Rap1 activation, causing platelet dysfunction.

David S. Paul, J. Hernández-Rivas, S. Watson, 2016, Blood.

Mutation in GNE is associated with severe congenital thrombocytopenia.

M. Simpson, S. Watson, J. Motwani, 2018, Blood.

1 MUTATION IN GNE IS ASSOCIATED WITH A SEVERE FORM OF CONGENITAL THROMBOCYTOPENIA

M. Simpson, S. Watson, J. Motwani, 2018 .

What is it like being a sibling of a child with cancer?

Ben Johnson, 2002, International journal of palliative nursing.

University of Birmingham Mutation in GNE is associated with a Severe Form of Congenital Thrombocytopenia

M. Simpson, S. Watson, J. Motwani, 2018 .

A comprehensive targeted next‐generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia

J. Thachil, M. Williams, N. Morgan, 2018, Research and practice in thrombosis and haemostasis.

Mutation in GNE is associated with severe congenital thrombocytopenia.

M. Simpson, S. Watson, J. Motwani, 2018, Blood.

A comprehensive targeted next‐generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia

J. Thachil, M. Williams, N. Morgan, 2018, Research and practice in thrombosis and haemostasis.