Nicholas A. Watkins
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 24 publications
Canadian Society of Nephrology Commentary on the 2025 Kidney Disease Improving Global Outcomes Clinical Practice Guidelines for Autosomal Dominant Polycystic Kidney Disease.
Journal: Canadian journal of kidney health and disease
Published: January 21, 2026
Advancing the Landscape of Clinical Actionability in Von Hippel-Lindau Syndrome: An Evidence-Based Framework from the INT2GRATE Oncology Consortium.
Journal: Cancers
Published: May 06, 2025
Framework for standardized genetic testing recommendations for chronic kidney disease in Ontario.
Journal: Genetics in medicine open
Published: April 07, 2025
Genetic counseling referral rates and genetic testing outcomes in women with young breast cancer: a 20-year Canadian review.
Journal: Breast cancer research and treatment
Published: November 08, 2024
Variant classification changes over time in the clinical molecular diagnostic laboratory setting.
Journal: Journal of medical genetics
Published: November 20, 2023
Validation of low-pass genome sequencing for prenatal diagnosis.
Journal: Prenatal diagnosis
Published: August 11, 2023
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 22, 2023
Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies.
Journal: Prenatal diagnosis
Published: September 18, 2021
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository.
Journal: Journal of medical genetics
Published: January 25, 2021
The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 30, 2020
Correction to: Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario.
Journal: Journal of cancer research and clinical oncology
Published: September 25, 2020
Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency.
Journal: Clinical genetics
Published: July 23, 2020
Last Updated: 09/26/2026