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Robin Z. Hayeems

The Hospital for Sick Children

33H-index
197Paper Count
4.0KCitation Count
Published Papers 87
Publication Date
Clinical Utility of Exome Sequencing: Post-Exome Testing Decision Changes in the Management of Children with Suspected Rare Genetic Disease
err2026-06-11
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errToni Tagimacruz; Trevor Adam Seeger; Koen Degeling; Katharine Fooks; Viji Venkataramanan; Francois P. Bernier; Kym M. Boycott; Roberto Mendoza-Londono; Taila Hartley; Robin Hayeems; Deborah A. Marshall
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Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS)
err2026-05-26
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PREAI
errSalma Shickh; Stephanie Luca; Katharine Fooks; Elise Poole; Bowen Xiao; Joyce Yan; Amanda Pichini; Joanna Ziff; Katrina Stone; Wendy J. Ungar; Pranesh Chakraborty; David Bick; Robin Z. Hayeems
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Correction: The development and usability of ‘The Genetics Navigator’: a digital solution for adult and paediatric clinical genetics services
err2026-04-02
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PREAI
errSaumeh Saeedi; Daena Hirjikaka; Marc Clausen; Stephanie Luca; Emma Reble; Rita Kodida; Daniel Assamad; Lauren Chad; Gregory Costain; Hanna Faghfoury; Josh Silver; Serena Shastri-Estrada; Maureen Smith; Robin Z. Hayeems; Yvonne Bombard
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Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
err2026-03-27
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PREAI
errAssamad, Daniel; Hansen, Abigail; Fooks, Katharine; Luca, Stephanie; Venkataramanan, Viji; Hsue, Erin; Shickh, Salma; Yan, Joyce; Wu, Vercancy; Badalato, Lauren; Balci, Tugce B.; Beausejour Ladouceur, Virginie; Chad, Lauren; Chisholm, Caitlin; Gillespie, Meredith K.; Huang, Lijia; Jarinova, Olga; Lau, Lynette; Lee, Whiwon; Mackley, Michael P.; Marshall, Christian R.; Mendoza-Londono, Roberto; Morel, Chantal F.; Richer, Julie; Sawyer, Sarah; Stavropoulos, Dimitri J.; Szuto, Anna; Tarnopolsky, Mark; Villani, Anita; Zahavich, Laura; Somerville, Martin J.; Boycott, Kym M.; Ungar, Wendy J.; Hayeems, Robin Z.
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The clinical utility of genome sequencing is multi-dimensional: experience from the Hong Kong Genome Project
err2026-02-20
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errAnnie Tsz Wai Chu; Claudia Ching Yan Chung; Ho Ming Luk; Shirley Sze Wing Cheng; Robin Hayeems; Stephanie Luca; Brian Hon Yin Chung
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A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohort
err2026-01-10
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errSalma Shickh; Katharine Fooks; Viji Venkataramanan; Meryl Acker; Karen V. MacDonald; Trevor A. Seeger; Meredith Gillespie; Taila Hartley; Kym M. Boycott; Francois Bernier; Deborah A. Marshall; Robin Z. Hayeems
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Experiencing acute genomic care: perspectives from parents in the neonatal and paediatric intensive care units towards rapid genomic sequencing
err2026-01-10
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PREAI
errMichael P. Mackley; Megan A. Dickson; Anna Szuto; James Anderson; David Chitayat; Robin Z. Hayeems; Roberto Mendoza-Londono; Eugene Ng; Martin Offringa; Yi Wen Wang; Linh G. Ly; Lauren Chad
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Barriers and facilitators to implementing clinical genome-wide sequencing: A scoping review of the global landscape
err2026-01-01
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PREAI
errLee, Whiwon; Yan, Joyce; Fooks, Katharine; Barwick, Melanie; Dobrow, Mark; Friedman, Jan M.; Marshall, Christian R.; Hayeems, Robin Z.
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Determining the value of genomics in healthcare
err2025-11-27
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PREAI
errIlias Goranitis; Robin Z. Hayeems; Hadley Stevens Smith; James Buchanan; Deirdre Weymann; Dean A. Regier; Michael P. Mackley; Richard H. Scott; Sue L. Hill; Brian H. Y. Chung; Claudia C. Y. Chung; Stephanie Best; Emma L. Baple; Zornitza Stark
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Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial
err2025-10-10
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PREAI
errRobin Z. Hayeems; Wendy J. Ungar; Christian R. Marshall; Meredith K. Gillespie; Anna Szuto; Lijia Huang; Viji Venkataramanan; Bowen Xiao; Caitlin Chisholm; D.James Stavropoulos; Mélanie Beaulieu Bergeron; Whiwon Lee; Gregory Costain; Rebekah Jobling; Sarah Sawyer; E.Magda Price; Lynette Lau; Roberto Mendoza; Martin J. Somerville; Kym M. Boycott
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A Microcosting and Cost Consequence Analysis from a Randomized Controlled Trial Comparing Genome Sequencing to Exome Sequencing for Genetic Diagnosis
err2025-08-21
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errWendy J. Ungar; Vercancy Wu; Christian R. Marshall; Jackie Hwang; Robin Z. Hayeems; Kate Tsiplova; Meredith K. Gillespie; Anna Szuto; Caitlin Chisholm; Dimitri J. Stavropoulos; Viji Venkataramanan; Bowen Xiao; Gregory Costain; Mélanie Beaulieu Bergeron; Sarah Sawyer; Lynette Lau; Lijia Huang; Roberto Mendoza-Londono; Martin J. Somerville; Kym M. Boycott
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Multiple domains of efficacy define the utility of genetic testing
err2025-07-23
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PREAI
errCatherine Marx; Amy Y. Pan; Robin Z. Hayeems; Gregory Costain
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The Clinician-reported Genetic Testing Utility InDEx for Neonatal Intensive Care (C-GUIDE NICU): Quantifying genome-wide sequencing utility in the NICU
err2025-06-18
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PREAI
errLena I. Dolman; Joyce Yan; Stephanie Luca; Bowen Xiao; Salma Shickh; Elise Poole; Lauren Chad; Wendy J. Ungar; Martin Offringa; Robin Z. Hayeems
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Mainstreaming of clinical genetic testing: A conceptual framework
err2025-05-22
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errMichael P. Mackley; Julie Richer; Andrea Guerin; Oana Caluseriu; Linlea Armstrong; Katherine A. Blood; Francois Bernier; Christie Boswell-Patterson; Marisa Chard; Gregory Costain; David Dyment; Alison Eaton; Hanna Faghfoury; Patrick Frosk; Meredith K. Gillespie; Elaine S. Goh; Robin Z. Hayeems; Bita Hashemi; A. Micheil Innes; Molly Jackson; Kym M. Boycott
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Non-geneticist champions are essential to the mainstreaming of genomic medicine
err2025-01-03
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errMackley, Michael P.; Weisz, Emma; Hayeems, Robin Z.; Gaff, Clara; Dawson-McClaren, Belinda
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The Clinician-reported Genetic Testing Utility Index (C-GUIDE) for Prenatal Care: Initial evidence of content and construct validity
err2025-01-01
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PREAI
errHayeems, Robin Z.; Luca, Stephanie; Xiao, Bowen; Boswell-Patterson, Christie; Venegas, Carolina Lavin; Semaan, Clarissa R. Abi; Kolar, Tessa; Myles-Reid, Diane; Chad, Lauren; Dyment, David; Boycott, Kym M.; Lazier, Joanna; Ungar, Wendy J.; Armour, Christine M.
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Exome Sequencing in the Diagnostic Pathway for Suspected Rare Genetic Diseases: Does the Order of Testing Affect its Cost-Effectiveness?
err2024-12-30
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PREAI
errDegeling, Koen; Tagimacruz, Toni; MacDonald, Karen, V; Seeger, Trevor A.; Fooks, Katharine; Venkataramanan, Viji; Boycott, Kym M.; Bernier, Francois P.; Mendoza-Londono, Roberto; Hartley, Taila; Hayeems, Robin Z.; Marshall, Deborah A.
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Development of a Value Assessment Framework for Pediatric Health Technologies Using Multicriteria Decision Analysis: Expanding the Value Lens for Funding Decision Making
err2024-07-01
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PREAI
errGauvreau, Cindy L.; Schreyer, Leighton; Gibson, Paul J.; Koo, Alicia; Ungar, Wendy J.; Regier, Dean; Chan, Kelvin; Hayeems, Robin; Gibson, Jennifer; Palmer, Antonia; Peacock, Stuart; Denburg, Avram E.
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Genetics providers ' perspectives on the use of digital tools in clinical practice
err2024-06-01
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PREAI
errLee, Whiwon; Hirjikaka, Daena; Grewal, Sonya; Shaw, Angela; Luca, Stephanie; Clausen, Marc; Bombard, Yvonne; Hayeems, Robin Z.
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Co-developing longitudinal patient registries for phenylketonuria and mucopolysaccharidoses in Canada
err2024-04-01
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PREAI
errAdams, John; Angel, Kim; Mitchell, John J.; Chakraborty, Pranesh; Potter, Beth K.; Inbar-Feigenberg, Michal; Stockler, Sylvia; Lamoureux, Monica; Howie, Alison; Pace, Alex; Butcher, Nancy J.; Rockman-Greenberg, Cheryl; Hayeems, Robin; Laberge, Anne-Marie; Lacaze-Masmonteil, Thierry; Round, Jeff; Offringa, Martin; Oksoui, Maryam; Schulze, Andreas; Speechley, Kathy; Thavorn, Kednapa; Trakadis, Yannis; Wilson, Kumanan
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