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The Canadian Journal of Cardiology
|
April 26, 2022
A Model for the Integration of Genome Sequencing Into a Pediatric Cardiology Clinic
Eriskay J Liston, Kelsey J Kalbfleisch, Kaitlin J Stanley, et al.
Canadian Urological Association Journal = Journal De L'Association Des Urologues Du Canada
|
June 25, 2021
The evolving role of germline genetic testing and management in prostate cancer: Report from the Princess Margaret Cancer Centre international retreat
Roderick Clark, Miran Kenk, Kristen McAlpine, et al.
American Journal of Human Genetics
|
October 6, 2023
Current and new frontiers in hereditary cancer surveillance: Opportunities for liquid biopsy
Kirsten M Farncombe, Derek Wong, Maia L Norman, et al.
BMJ Open
|
November 24, 2024
Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocol
Kirsten M Farncombe, Lauren K Hughes, Elif Tuzlali, et al.
Human Mutation
|
April 27, 2022
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease
Andreea Chiorean, Kirsten M Farncombe, Sean Delong, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 5, 2025
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel Lindau (VHL) Disease
D I Ritter, C Badduke, K Doonanco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 3, 2026
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel-Lindau (VHL) Disease
Deborah I Ritter, Chansonette Badduke, Kurston Doonanco, et al.
European Journal of Human Genetics : EJHG
|
January 29, 2026
Non-invasive screening in hereditary cancer: a randomized controlled trial to test cell-free DNA-based early detection in the CHARM consortium
Kirsten M Farncombe, Julia A Sobotka, Melyssa Aronson, et al.
Cancer Discovery
|
October 24, 2023
Early Cancer Detection in Li-Fraumeni Syndrome with Cell-Free DNA
Derek Wong, Ping Luo, Leslie E Oldfield, et al.
Nature Cancer
|
May 27, 2022
A community approach to the cancer-variant-interpretation bottleneck
Kilannin Krysiak, Arpad M Danos, Susanna Kiwala, et al.
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Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
The Canadian Journal of Cardiology
|
April 26, 2022
A Model for the Integration of Genome Sequencing Into a Pediatric Cardiology Clinic
Eriskay J Liston, Kelsey J Kalbfleisch, Kaitlin J Stanley, et al.
Canadian Urological Association Journal = Journal De L'Association Des Urologues Du Canada
|
June 25, 2021
The evolving role of germline genetic testing and management in prostate cancer: Report from the Princess Margaret Cancer Centre international retreat
Roderick Clark, Miran Kenk, Kristen McAlpine, et al.
American Journal of Human Genetics
|
October 6, 2023
Current and new frontiers in hereditary cancer surveillance: Opportunities for liquid biopsy
Kirsten M Farncombe, Derek Wong, Maia L Norman, et al.
BMJ Open
|
November 24, 2024
Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocol
Kirsten M Farncombe, Lauren K Hughes, Elif Tuzlali, et al.
Human Mutation
|
April 27, 2022
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease
Andreea Chiorean, Kirsten M Farncombe, Sean Delong, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 5, 2025
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel Lindau (VHL) Disease
D I Ritter, C Badduke, K Doonanco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 3, 2026
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel-Lindau (VHL) Disease
Deborah I Ritter, Chansonette Badduke, Kurston Doonanco, et al.
European Journal of Human Genetics : EJHG
|
January 29, 2026
Non-invasive screening in hereditary cancer: a randomized controlled trial to test cell-free DNA-based early detection in the CHARM consortium
Kirsten M Farncombe, Julia A Sobotka, Melyssa Aronson, et al.
Cancer Discovery
|
October 24, 2023
Early Cancer Detection in Li-Fraumeni Syndrome with Cell-Free DNA
Derek Wong, Ping Luo, Leslie E Oldfield, et al.
Nature Cancer
|
May 27, 2022
A community approach to the cancer-variant-interpretation bottleneck
Kilannin Krysiak, Arpad M Danos, Susanna Kiwala, et al.
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of 4