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Matthew S Lebo

Showing results (51-60 of 69) with videos related to

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American Journal of Human Genetics|November 3, 2023
The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary careJason L Vassy, Charles A Brunette, Matthew S Lebo, et al.
The Lancet. Haematology|May 22, 2018
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing studyWilliam J Lane, Connie M Westhoff, Nicholas S Gleadall, et al.
Nature Communications|November 26, 2025
Genetics and context for precision health in Greater BostonSatoshi Koyama, Ying Wang, Kaavya Paruchuri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)Matthew S Lebo, Kathleen-Rose Zakoor, Kathy Chun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2023
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working GroupRyan J Schmidt, Marcie Steeves, Pinar Bayrak-Toydemir, et al.
American Journal of Human Genetics|August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research CohortMarci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2017
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centersRashesh V Sanghvi, Christian J Buhay, Bradford C Powell, et al.
Journal of Medical Genetics|April 20, 2021
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics RepositoryChloe Mighton, Amanda C Smith, Justin Mayers, et al.
American Journal of Human Genetics|May 17, 2016
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research ConsortiumLaura M Amendola, Gail P Jarvik, Michael C Leo, et al.
American Journal of Human Genetics|July 9, 2016
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research ConsortiumLaura M Amendola, Gail P Jarvik, Michael C Leo, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|November 3, 2023
The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary careJason L Vassy, Charles A Brunette, Matthew S Lebo, et al.
The Lancet. Haematology|May 22, 2018
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing studyWilliam J Lane, Connie M Westhoff, Nicholas S Gleadall, et al.
Nature Communications|November 26, 2025
Genetics and context for precision health in Greater BostonSatoshi Koyama, Ying Wang, Kaavya Paruchuri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)Matthew S Lebo, Kathleen-Rose Zakoor, Kathy Chun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2023
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working GroupRyan J Schmidt, Marcie Steeves, Pinar Bayrak-Toydemir, et al.
American Journal of Human Genetics|August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research CohortMarci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2017
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centersRashesh V Sanghvi, Christian J Buhay, Bradford C Powell, et al.
Journal of Medical Genetics|April 20, 2021
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics RepositoryChloe Mighton, Amanda C Smith, Justin Mayers, et al.
American Journal of Human Genetics|May 17, 2016
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research ConsortiumLaura M Amendola, Gail P Jarvik, Michael C Leo, et al.
American Journal of Human Genetics|July 9, 2016
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research ConsortiumLaura M Amendola, Gail P Jarvik, Michael C Leo, et al.
Pageof 7