Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Eric Venner

Showing results (11-20 of 41) with videos related to

Pageof 5
Sort By:
Journal of the American Medical Informatics Association : JAMIA|March 6, 2024
Empowering personalized pharmacogenomics with generative AI solutionsMullai Murugan, Bo Yuan, Eric Venner, et al.
Molecular Genetics & Genomic Medicine|January 24, 2020
Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemiaJidong Liu, Guolian Ding, Kexin Zou, et al.
The Journal of Molecular Diagnostics : JMD|May 9, 2025
Clinical Bioinformatician Body of Knowledge-Clinical Laboratory Regulation and Data Security Core: A Report of the Association for Molecular PathologyRyan J Schmidt, Larissa V Furtado, Amber M Fussell, et al.
Life (Basel, Switzerland)|February 25, 2022
Artificial Intelligence and Cardiovascular GeneticsChayakrit Krittanawong, Kipp W Johnson, Edward Choi, et al.
American Journal of Human Genetics|June 15, 2021
Exome variant discrepancies due to reference-genome differencesHe Li, Moez Dawood, Michael M Khayat, 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.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
<i>Celeste</i>: A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projectsNoora Siddiqui, Breanna Lee, Victoria Yi, et al.
Medrxiv : the Preprint Server for Health Sciences|July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us ParticipantsAndrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology|February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
Communications Biology|June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Journal of the American Medical Informatics Association : JAMIA|March 6, 2024
Empowering personalized pharmacogenomics with generative AI solutionsMullai Murugan, Bo Yuan, Eric Venner, et al.
Molecular Genetics & Genomic Medicine|January 24, 2020
Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemiaJidong Liu, Guolian Ding, Kexin Zou, et al.
The Journal of Molecular Diagnostics : JMD|May 9, 2025
Clinical Bioinformatician Body of Knowledge-Clinical Laboratory Regulation and Data Security Core: A Report of the Association for Molecular PathologyRyan J Schmidt, Larissa V Furtado, Amber M Fussell, et al.
Life (Basel, Switzerland)|February 25, 2022
Artificial Intelligence and Cardiovascular GeneticsChayakrit Krittanawong, Kipp W Johnson, Edward Choi, et al.
American Journal of Human Genetics|June 15, 2021
Exome variant discrepancies due to reference-genome differencesHe Li, Moez Dawood, Michael M Khayat, 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.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
<i>Celeste</i>: A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projectsNoora Siddiqui, Breanna Lee, Victoria Yi, et al.
Medrxiv : the Preprint Server for Health Sciences|July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us ParticipantsAndrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology|February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
Communications Biology|June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
Pageof 5