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Robin Z. Hayeems

Observed names: Hayeems Robin Z, Hayeems, Robin Zoe, R Z Hayeems, R. Z. Hayeems, R.Z. Hayeems, R.Z., Hayeems, ROBIN Z. HAYEEMS, RZ Hayeems, Robin Hayeems, Robin Z Hayeems, Robin Zoe Hayeems, Robyn Hayeems
Observed institutions: St. Michael's Hospital, University Health Network, University of Arizona, University of Ottawa, University of Toronto, Children's Hospital of Eastern Ontario, Great Ormond Street Hospital, Hospital for Sick Children, Toronto General Hospital, Ted Rogers Centre for Heart Research, SickKids Foundation, Unity Health Toronto, University of Arizona College of Medicine- Phoenix, Sickkids Research Institute, Arizona State University
ORCID: 0000-0003-3269-8004
Observed ORCID: 0000-0003-3269-8004
OpenAlex ID: A5044819903
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
2017 · Anath C. Lionel, Gregory Costain, et al. · Genetics in Medicine · 557
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Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine
2016 · Dimitri J Stavropoulos, Daniele Merico, et al. · npj Genomic Medicine · 366
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Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care
2013 · Fiona A Miller, Robin Z Hayeems, et al. · European Journal of Human Genetics · 117
Health system strategies supporting transition to adult care
2015 · Charlotte Moore Hepburn, Eyal Cohen, et al. · Archives of Disease in Childhood · 103
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Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity
2020 · Gregory Costain, Susan Walker, et al. · JAMA Network Open · 91
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The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease
2020 · Miriam S. Reuter, Rajiv R. Chaturvedi, et al. · Genetics in Medicine · 90
Clinical utility of genomic sequencing: a measurement toolkit
2020 · Robin Z. Hayeems, David Dimmock, et al. · npj Genomic Medicine · 84
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Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
2016 · J A Anderson, M S Meyn, et al. · Journal of Medical Ethics · 83
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
2023 · Alissa M D'Gama, Sarah Mulhern, et al. · The Lancet Neurology · 78
Experiences of caregivers of children with inherited metabolic diseases: a qualitative study
2016 · Shabnaz Siddiq, Brenda J. Wilson, et al. · Orphanet Journal of Rare Diseases · 75
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Data-driven consideration of genetic disorders for global genomic newborn screening programs
2025 · Thomas Minten, Sarah Bick, et al. · Genetics in Medicine · 73
Public views on participating in newborn screening using genome sequencing
2014 · Yvonne Bombard, Fiona A Miller, et al. · European Journal of Human Genetics · 68
How patients experience progressive loss of visual function: a model of adjustment using qualitative methods
2005 · R Z Hayeems · British Journal of Ophthalmology · 68
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Patient-facing digital tools for delivering genetic services: a systematic review
2022 · Whiwon Lee, Salma Shickh, et al. · Journal of Medical Genetics · 61
What is a meaningful result? Disclosing the results of genomic research in autism to research participants
2010 · Fiona Alice Miller, Robin Zoe Hayeems, et al. · European Journal of Human Genetics · 58
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How digital tools can advance quality and equity in genomic medicine
2020 · Yvonne Bombard, Robin Z. Hayeems · Nature Reviews Genetics · 55
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Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening
2010 · Yvonne Bombard, Fiona A Miller, et al. · European Journal of Human Genetics · 53
Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study
2017 · Iris Cohn, Tara A. Paton, et al. · npj Genomic Medicine · 52
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The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine
2015 · S.C. Bowdin, R.Z. Hayeems, et al. · Clinical Genetics · 49
Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting
2021 · Iris Cohn, Roozbeh Manshaei, et al. · JAMA Network Open · 48
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Predictive genetic testing for adult‐onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines
2014 · J.A. Anderson, R.Z. Hayeems, et al. · Clinical Genetics · 47
A Systematic Review of the Effects of Disclosing Carrier Results Generated Through Newborn Screening
2008 · R. Z. Hayeems, J. P. Bytautas, et al. · Journal of Genetic Counseling · 47
Citizens’ Values Regarding Research With Stored Samples From Newborn Screening in Canada
2012 · Yvonne Bombard, Fiona A. Miller, et al. · PEDIATRICS · 46
Utility of Genetic Testing from the Perspective of Parents/Caregivers: A Scoping Review
2021 · Robin Z. Hayeems, Stephanie Luca, et al. · Children · 45
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Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis
2017 · Robin Z. Hayeems, Fiona A. Miller, et al. · The Journal of Pediatrics · 45
Works count: 204
Citation count: 4,123
H-index: 36
I10-index: 92
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