Mark Skinner

Assistant Professor (part-time)

McMaster University

Canada

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Mark Skinner is an Assistant Professor (part-time) at McMaster University in Canada. His research primarily focuses on hemophilia and bleeding disorders, with recent articles exploring patient-reported outcomes, quality of life, and treatment methodologies. He is actively engaged in advancing knowledge and practices in gene-targeted therapies within the field of rare diseases.

Articles (17)

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2025

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2025

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2024

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2024

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2024

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2024

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2024

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2022

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2022

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2022

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2022

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2022

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2021

Collaborators (10)

Alfonso Iorio

Professor

McMaster University

CANADA

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AMY DUNN

Assistant Professor of Pediatrics

Emory University School of Medicine

UNITED STATES

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Aaron J. Goldenberg

UNITED STATES

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Erik Berntorp

Lund University

SWEDEN

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Tyler Buckner

Assistant Professor

University of Colorado School of Medicine

UNITED STATES

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Craig M. Kessler

UNITED STATES

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Barbara Konkle

Professor of Medicine

University of Washington

UNITED STATES

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Miguel Escobar

Professor (Tenure)

The University of Texas MD Anderson Cancer Center

UNITED STATES

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Erika Augustine

Kennedy Krieger Institute

UNITED STATES

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Federico Germini

Assistant Professor

McMaster University

ITALY

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Mark Skinner

Research Interests

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Articles (17)

Feasibility of Administering the Patient Reported Outcomes, Burdens and Experiences (PROBE) Questionnaire Through the Canadian Bleeding Disorders Registry (CBDR) and Comparison of Data From the Two Sources

Pain‐Related Quality of Life Outcomes in People With Haemophilia A Receiving Emicizumab: A Post Hoc Analysis of the HAVEN 1, 3 and 4 and STASEY Studies

Association of patient, treatment and disease characteristics with patient‐reported outcomes: Results of the ECHO Registry

Contrasting Approaches in the Implementation of GRADE Methodology in Guidelines for Haemophilia and Von Willebrand Disease

International Society on Thrombosis and Haemostasis Clinical Practice Guideline for Treatment of Congenital Haemophilia—A Critical Appraisal

Development of the World Federation of Hemophilia Shared Decision‐Making Tool

Development of the coreHEM mental health patient‐reported outcome measure – A novel mental health outlook measure for people with haemophilia

Prophylaxis use of clotting factor replacement products in people with non‐severe haemophilia: A review of the literature

Data sharing to advance gene‐targeted therapies in rare diseases

Hemophilia gene therapy: first, do no harm

Gene‐targeted therapies: Towards equitable development, diagnosis, and access

Achieving access to haemophilia care in low-income and lower-middle-income countries: expanded Humanitarian Aid Program of the World Federation of Hemophilia after 5 years

User-Centered Development and Testing of the Online Patient-Reported Outcomes, Burdens, and Experiences (PROBE) Survey and the myPROBE App and Integration With the Canadian Bleeding Disorder Registry: Mixed Methods Study

Association of factor expression levels with health-related quality of life and direct medical costs for people with haemophilia B

The Hemophilia Gene Therapy Patient Journey: Questions and Answers for Shared Decision-Making

A preliminary application of a haemophilia value framework to emerging therapies in haemophilia

Patient preferences and priorities for haemophilia gene therapy in the US: A discrete choice experiment

Collaborators (10)

Alfonso Iorio

AMY DUNN

Aaron J. Goldenberg

Erik Berntorp

Tyler Buckner

Craig M. Kessler

Barbara Konkle

Miguel Escobar

Erika Augustine

Federico Germini

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