Catherine Hayward

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McMaster University

Canada

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About

Professor Catherine Hayward is a faculty member at McMaster University in Canada. Her research focuses on coagulopathies, including congenital and acquired disorders, and she has published recent articles on topics such as vitamin K deficiency, platelet aggregation, and the management of rare bleeding disorders. Through her work, she aims to enhance the diagnosis and treatment of complex hematological conditions.

Recent Grants

Grant: Close

Characterization of common inherited platelet function disorders

Open Date: 2014-04-01

Close Date: 2016-03-01

Grant: Close

Multimerin 1 functions in platelet adhesion and thrombus formation

Open Date: 2014-04-01

Close Date: 2019-03-31

Grant: Close

Multimerin 1 functions as a binding protein for multiple components of prothrombinase

Open Date: 2011-07-01

Close Date: 2013-06-01

Grant: Close

Specialized care of patients with bleeding disorders

Open Date: 2010-07-01

Close Date: 2011-03-01

Grant: Close

Molecular Basis of Profibrinolytic Platelets and White Blood Cells in Quebec Platelet Disorder.

Open Date: 2009-10-01

Close Date: 2014-09-30

Articles (19)

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2025

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2021

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2021

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2020

Collaborators (4)

Donald Arnold

Professor

McMaster University

CANADA

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Stephanie Smith

Research Assistant Professor

University of Michigan

UNITED STATES

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Marie-christine ALESSI

Professor / Director

Aix-Marseille University

FRANCE

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Stella Thomassen

Chief Marketing Officer

NETHERLANDS

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Catherine Hayward

Research Interests

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About

Recent Grants

Articles (19)

Laboratory diagnosis of congenital and acquired coagulopathies, including challenging-to-diagnose rare bleeding disorders

Case Report: Tranexamic Acid Therapy Corrects the Impaired Epinephrine Aggregation Responses of Quebec Platelet Disorder

Vitamin K Deficiency: Diagnosis and Management

How Trustworthy is Light Transmittance Platelet Aggregometry With Low Platelet Count Samples? Insights From Test Replicates and Retrospective Analysis of Several Decades of Diagnostic Samples

“Discrepant low von Willebrand factor activity results on the ACL TOP analyzer are frequent in unselected patients with myeloproliferative neoplasms and show no correlation with high-molecular-weight multimer loss or bleeding phenotype”: comment from Al Sharif et al.

Measurement of factor XIII for the diagnosis and management of deficiencies: insights from a retrospective review of 10 years of data on consecutive samples and patients

Evaluation of a diagnostic platelet aggregation test strategy for platelet rich plasma samples with low platelet counts

Rapid diagnosis of coagulopathies from vitamin K deficiency in a consecutive case cohort evaluated by comparative assessment of factor II by 1-stage assays with prothrombin time vs Ecarin reagents

Rare bleeding disorders: Advances in management

Rare inherited coagulation and fibrinolytic defects that challenge diagnostic laboratories

Memorial notice: William L. Nichols, MD

Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for ultra-rare inherited bleeding disorders

Update on platelet procoagulant mechanisms in health and in bleeding disorders

Screening and diagnosis of inherited platelet disorders

Severe thrombophilia in a factor V‐deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)

Thrombin generation abnormalities in commonly encountered platelet function disorders

Memorial notice: Elizabeth M. Van Cott MD

Unraveling von Willebrand factor deficiency

Improved platelet counts during prolonged tranexamic therapy for Quebec platelet disorder implicate the underlying fibrinolytic defect as the cause of lower platelet counts

Collaborators (4)

Donald Arnold

Stephanie Smith

Marie-christine ALESSI

Stella Thomassen

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