B. Dawood

发表

Src family kinases are essential for primary aggregation by Gi‐coupled receptors

S. Watson, Y. Senis, A. Mumford, 2010, Journal of thrombosis and haemostasis : JTH.

A novel thromboxane A2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis.

S. Mundell, S. Watson, M. Wheatley, 2010, Blood.

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

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

Phenotypic approaches to gene mapping in platelet function disorders

S. Mundell, S. Watson, Jonathan J. Wilde, 2010, Hämostaseologie.

University of Birmingham Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

S. Watson, M. Lordkipanidzé, A. Mumford, 2012 .

Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study.

S. Mundell, S. Watson, F. Rodeghiero, 2009, Blood.

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.

M. Simpson, S. Watson, M. Lordkipanidzé, 2013, Blood.

MYBL2 haploinsufficiency increases susceptibility to age-related haematopoietic neoplasia

R. Kralovics, J. Frampton, R. Jäger, 2012, Leukemia.

Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy).

D. Chitayat, S. Watson, M. Donowitz, 2010, Gastroenterology.

MCMDM-1VWD study diagnosed with type 1 von Willebrand disease in the European variant in a patient 12 Identification and characterization of a novel P2Y

S. Watson, F. Rodeghiero, A. Mumford, 2012 .

MCMDM-1 VWD study diagnosed with type 1 von Willebrand disease in the European variant in a patient 12 Identification and characterization of a novel P 2 Y

S. Watson, F. Rodeghiero, A. Mumford, 2009 .

Identification and characterization of a novel P 2 Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1 VWD study

S. Mundell, S. Watson, F. Rodeghiero, 2009 .

Endoscopic Findings in Persistent Dyspepsia in Secondary Care Hospital Setting in North Kashmir.

B. Dawood, R. Andrabi, S. Mushtaq, 2019, The Journal of the Association of Physicians of India.

binding in a patient with a bleeding diathesis receptor D304N variant that abrogates ligand 2 A novel thromboxane A

S. Mundell, S. Watson, M. Wheatley, 2010 .

A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8).

Colin A. Johnson, S. Watson, R. Trembath, 2006, American journal of human genetics.

Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders

M. Lordkipanidzé, S. Heptinstall, S. Watson, 2014, Journal of thrombosis and haemostasis : JTH.

Reference curves for aggregation and ATP secretion to aid diagnose of platelet-based bleeding disorders: Effect of inhibition of ADP and thromboxane A2 pathways

S. Watson, J. Wilde, B. Dawood, 2007, Platelets.

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

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

A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction

S. Mundell, S. Watson, M. Lordkipanidzé, 2014, Thrombosis and Haemostasis.

agonist panel disorders including recommendation and validation of a streamlined Evaluation of participants with suspected heritable platelet function

S. Watson, M. Lordkipanidzé, A. Mumford, 2012 .

A Germline Mutation in BLOC 1 S 3 / Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome ( HPS 8 )

Colin A. Johnson, S. Watson, R. Trembath, 2005 .

Prescribing patterns of oral antiplatelets in Wales: evolving trends from 2005 to 2016.

M. Protty, B. Dawood, J. Hayes, 2018, Future cardiology.

Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy).

D. Chitayat, S. Watson, M. Donowitz, 2010, Gastroenterology.

University of Birmingham Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

S. Watson, M. Lordkipanidzé, A. Mumford, 2012 .