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Robin Hayeems

Senior Scientist

Hospital for Sick Children

Canada

Research Interests

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Professors in Canada

Articles (20)

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2026

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Collaborators (17)

Ian D Graham

Distinguished Professor

University of Ottawa

CANADA

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Raymond H. Kim

University Health Network

CANADA

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Cheryl Rockman-Greenberg

Medical/Metabolic Geneticist

Shared Health Manitoba

CANADA

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Emma Baple

Professor of Genomic Medicine, Consultant Clinical Genetics

University of Exeter

UNITED KINGDOM

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Linlea Armstrong

Clinical Associate Professor

The University of British Columbia

CANADA

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Roberto Mendoza‐Londono

CANADA

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Christian Marshall

Clinical Laboratory Director

Hospital for Sick Children

CANADA

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Michael Wilson

Associate Professor

McMaster University

CANADA

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Toni Tagimacruz

Assistant Professor

Trinity Western University

CANADA

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James Buchanan

Senior Lecturer

Queen Mary University of London

UNITED KINGDOM

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Francois Bernier

Professor

University of Calgary

CANADA

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Deborah Marshall

University of Calgary

CANADA

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Alison Elliott

Associate Professor

The University of British Columbia

CANADA

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Wendy Ungar

Senior Scientist

Hospital for Sick Children

CANADA

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Gregory Costain

Hospital for Sick Children

CANADA

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Audrey L'Espérance

Assistant Professor in Health and Social Services Management

École nationale d'administration publique

CANADA

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Avram Denburg

Associate Professor (Status-Only)

University of Toronto

CANADA

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Robin Hayeems

Research Interests

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Articles (20)

Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS)

Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial

Patients' and parents' views on how digital tools enable personalized and partnered care in genetics: a qualitative study.

The Patient-reported Genetic testing Utility InDEx: A novel measure of personal utility.

Clinical utility of exome sequencing: Post-exome testing decision changes in the management of children with suspected rare genetic disease.

The impacts of caring for children with inherited metabolic diseases for families: a cross-sectional study.

Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing.

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study.

The clinical utility of genome sequencing is multi-dimensional: experience from the Hong Kong Genome Project.

Experiencing acute genomic care: perspectives from parents in the neonatal and paediatric intensive care units towards rapid genomic sequencing.

A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohort.

Protocol for the development of a core outcome set for type 1 diabetes risk screening

TRIAGE-GS: protocol for a randomised controlled trial of a genomics-first approach to rare disease diagnosis for patients awaiting assessment by a clinical geneticist

Barriers and facilitators to implementing clinical genome-wide sequencing: A scoping review of the global landscape.

Determining the value of genomics in healthcare.

General Population Screening for Type 1 Diabetes in Canada---CanScreenT1D.

Integrating paediatric subspecialists into the delivery of genomic medicine: A qualitative study

How does personal utility depend on clinical setting? Evidence from 3 cohorts

Multiple domains of efficacy define the utility of genetic testing.

The Clinician-reported Genetic Testing Utility InDEx for Neonatal Intensive Care (C-GUIDE NICU): Quantifying genome-wide sequencing utility in the NICU.

Collaborators (17)

Ian D Graham

Raymond H. Kim

Cheryl Rockman-Greenberg

Emma Baple

Linlea Armstrong

Roberto Mendoza‐Londono

Christian Marshall

Michael Wilson

Toni Tagimacruz

James Buchanan

Francois Bernier

Deborah Marshall

Alison Elliott

Wendy Ungar

Gregory Costain

Audrey L'Espérance

Avram Denburg

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