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Heidi L Rehm

Showing results (151-160 of 342) with videos related to

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The New England Journal of Medicine|June 30, 2021
Problems with Using Polygenic Scores to Select EmbryosPatrick Turley, Michelle N Meyer, Nancy Wang, et al.
Human Mutation|December 19, 2021
Harmonizing variant classification for return of results in the All of Us Research ProgramSteven M Harrison, Christina A Austin-Tse, Serra Kim, et al.
Nature Communications|October 6, 2025
Improved allele frequencies in gnomAD through local ancestry inferencePragati Kore, Michael W Wilson, Grace Tiao, et al.
Science Translational Medicine|November 11, 2016
Aggregate penetrance of genomic variants for actionable disorders in European and African AmericansPradeep Natarajan, Nina B Gold, Alexander G Bick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 3, 2026
ClinGen Variant Curation Interface Workshops: Training Variant Scientists on an International PlatformDeborah I Ritter, Mark Mandell, Christine Preston, et al.
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
Human Mutation|October 13, 2018
ClinGen advancing genomic data-sharing standards as a GA4GH driver projectLena Dolman, Angela Page, Lawrence Babb, et al.
Human Mutation|September 22, 2018
matchbox: An open-source tool for patient matching via the Matchmaker ExchangeHarindra Arachchi, Monica H Wojcik, Benjamin Weisburd, et al.
Current Protocols in Human Genetics|October 19, 2017
Matchmaker ExchangeNara L M Sobreira, Harindra Arachchi, Orion J Buske, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Discordant results between conventional newborn screening and genomic sequencing in the BabySeq ProjectMonica H Wojcik, Tian Zhang, Ozge Ceyhan-Birsoy, et al.
Pageof 35

Showing results (151-160 of 342) with videos related to

Sort By:
Pageof 35
The New England Journal of Medicine|June 30, 2021
Problems with Using Polygenic Scores to Select EmbryosPatrick Turley, Michelle N Meyer, Nancy Wang, et al.
Human Mutation|December 19, 2021
Harmonizing variant classification for return of results in the All of Us Research ProgramSteven M Harrison, Christina A Austin-Tse, Serra Kim, et al.
Nature Communications|October 6, 2025
Improved allele frequencies in gnomAD through local ancestry inferencePragati Kore, Michael W Wilson, Grace Tiao, et al.
Science Translational Medicine|November 11, 2016
Aggregate penetrance of genomic variants for actionable disorders in European and African AmericansPradeep Natarajan, Nina B Gold, Alexander G Bick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 3, 2026
ClinGen Variant Curation Interface Workshops: Training Variant Scientists on an International PlatformDeborah I Ritter, Mark Mandell, Christine Preston, et al.
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
Human Mutation|October 13, 2018
ClinGen advancing genomic data-sharing standards as a GA4GH driver projectLena Dolman, Angela Page, Lawrence Babb, et al.
Human Mutation|September 22, 2018
matchbox: An open-source tool for patient matching via the Matchmaker ExchangeHarindra Arachchi, Monica H Wojcik, Benjamin Weisburd, et al.
Current Protocols in Human Genetics|October 19, 2017
Matchmaker ExchangeNara L M Sobreira, Harindra Arachchi, Orion J Buske, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Discordant results between conventional newborn screening and genomic sequencing in the BabySeq ProjectMonica H Wojcik, Tian Zhang, Ozge Ceyhan-Birsoy, et al.
Pageof 35