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

Jonathan S Berg

Showing results (111-120 of 168) with videos related to

Pageof 17
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 12, 2017
CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencingRobert C Green, Jonathan S Berg, Wayne W Grody, et al.
The New England Journal of Medicine|May 28, 2015
ClinGen--the Clinical Genome ResourceHeidi L Rehm, Jonathan S Berg, Lisa D Brooks, et al.
Circulation. Cardiovascular Genetics|June 15, 2017
Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular DiseaseGloria T Haskell, Brian C Jensen, Leigh Ann Samsa, et al.
Public Health Genomics|April 21, 2025
Age-Based Genomic Screening: Pediatric Providers' Perspectives on ImplementationMargaret Waltz, Ann Katherine M Foreman, Rebecca A Gibson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2017
Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testingPatricia Himes, Tia L Kauffman, Kristin R Muessig, et al.
Genome Medicine|January 2, 2020
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation frameworkSarah E Brnich, Ahmad N Abou Tayoun, Fergus J Couch, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 15, 2022
Newborn screening for neurodevelopmental diseases: Are we there yet?Wendy K Chung, Jonathan S Berg, Jeffrey R Botkin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2017
Navigating the research-clinical interface in genomic medicine: analysis from the CSER ConsortiumSusan M Wolf, Laura M Amendola, Jonathan S Berg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2017
Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesNeeta L Vora, Bradford Powell, Alicia Brandt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 8, 2013
Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research ConsortiumJonathan S Berg, Laura M Amendola, Christine Eng, et al.
Pageof 17

Showing results (111-120 of 168) with videos related to

Sort By:
Pageof 17
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 12, 2017
CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencingRobert C Green, Jonathan S Berg, Wayne W Grody, et al.
The New England Journal of Medicine|May 28, 2015
ClinGen--the Clinical Genome ResourceHeidi L Rehm, Jonathan S Berg, Lisa D Brooks, et al.
Circulation. Cardiovascular Genetics|June 15, 2017
Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular DiseaseGloria T Haskell, Brian C Jensen, Leigh Ann Samsa, et al.
Public Health Genomics|April 21, 2025
Age-Based Genomic Screening: Pediatric Providers' Perspectives on ImplementationMargaret Waltz, Ann Katherine M Foreman, Rebecca A Gibson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2017
Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testingPatricia Himes, Tia L Kauffman, Kristin R Muessig, et al.
Genome Medicine|January 2, 2020
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation frameworkSarah E Brnich, Ahmad N Abou Tayoun, Fergus J Couch, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 15, 2022
Newborn screening for neurodevelopmental diseases: Are we there yet?Wendy K Chung, Jonathan S Berg, Jeffrey R Botkin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2017
Navigating the research-clinical interface in genomic medicine: analysis from the CSER ConsortiumSusan M Wolf, Laura M Amendola, Jonathan S Berg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2017
Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesNeeta L Vora, Bradford Powell, Alicia Brandt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 8, 2013
Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research ConsortiumJonathan S Berg, Laura M Amendola, Christine Eng, et al.
Pageof 17