M. Makris

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.

Guideline on the management of bleeding in patients on antithrombotic agents

M. Laffan, A. Mumford, C. Tait, 2013, British journal of haematology.

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

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

Whole genome sequencing of a sporadic primary immunodeficiency cohort

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2018, Nature.

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 .

Enzymatically catalyzed disulfide exchange is required for platelet adhesion to collagen via integrin α2β1

D. Essex, R. Farndale, J. Lahav, 2003 .

Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes

P. Heath, B. Wagner, N. Morgan, 2022, Haematologica.

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.

Clinical Features of Vaccine-Induced Immune Thrombocytopenia and Thrombosis

G. Ambler, S. Pavord, B. Hunt, 2021, The New England journal of medicine.

A ploidy-agnostic method for estimating telomere length from whole genome sequencing data.

Ania, Eleanor, Dewhurst, 2018 .

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 .

Emicizumab is a recombinant, humanised bispecific monoclonal antibody that binds factor IXa and factor X. Although emicizumab mimics factor VIII, in that it enhances factor IXa- mediated factor X activation, its mechanism of action

M. Makris, A. Iorio, PJ Lenting, 2020 .

Phase 1-2 Trial of AAVS3 Gene Therapy in Patients with Hemophilia B.

E. Tuddenham, G. Dolan, A. Dane, 2022, The New England journal of medicine.

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Henning Gall, Fengyuan Hu, Kevin Rue-Albrecht, 2018, American journal of human genetics.

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.

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2020, Nature.

Enzymatically catalyzed disulfide exchange is required for platelet adhesion to collagen via integrin alpha2beta1.

D. Essex, R. Farndale, J. Lahav, 2003, Blood.

Vaccine‐induced immune thrombotic thrombocytopenia (VITT): Update on diagnosis and management considering different resources

A. Greinacher, S. Pavord, M. Pai, 2021, Journal of Thrombosis and Haemostasis.

Lack of association between polymorphisms in the interleukin-1 gene cluster and familial thrombophilia.

A. Cox, M. Daly, M. Makris, 2012, Thrombosis research.

Natural history of PF4 antibodies in vaccine-induced immune thrombocytopenia and thrombosis

S. Pavord, W. Thomas, W. Lester, 2022, Blood.

Vaccine‐induced immune thrombotic thrombocytopenia (VITT) ‐ update on diagnosis and management considering different resources: Response to Comment from Yamada et al

A. Greinacher, S. Pavord, M. Pai, 2022, Journal of thrombosis and haemostasis : JTH.

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 .

Major Structural Defects in the Antithrombin Gene in Four Families with Type I Antithrombin Deficiency

M. Makris, F. Preston, I. Peake, 2000, Thrombosis and Haemostasis.

Null Alleles Are not a Common Cause of Type 1 von Willebrand Disease in the British Population

A. Goodeve, I. Peake, M. Daly, 1999, Thrombosis and Haemostasis.

Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: A EHA Consensus Report

P. Noris, A. Tosetto, F. Leebeek, 2019 .

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Andy G Lynch, Sri V. V. Deevi, Eleanor F. Dewhurst, 2017, Scientific Reports.

Impact of thromboprophylaxis on hospital acquired thrombosis following discharge in patients admitted with COVID‐19: Multicentre observational study in the UK

M. Laffan, D. Arachchillage, M. Makris, 2023, British Journal of Haematology.

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.

Guideline on the management of bleeding in patients on antithrombotic agents

M. Laffan, A. Mumford, C. Tait, 2013, British journal of haematology.

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.

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Sri V. V. Deevi, Eleanor F. Dewhurst, Courtney E. French, 2017, Scientific Reports.

Autoimmune disease and COVID-19: a multicentre observational study in the United Kingdom

Hakeem O. Yusuff, M. Laffan, J. Kilner, 2022, Rheumatology.

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 .