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Jonathan S Berg

Showing results (41-50 of 168) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2012
An informatics approach to analyzing the incidentalomeJonathan S Berg, Michael Adams, Nassib Nassar, et al.
Genome Medicine|December 1, 2019
Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert PanelsDona M Kanavy, Shannon M McNulty, Meera K Jairath, et al.
The Journal of Pediatrics|March 27, 2007
Ethical and legal implications of genetic testing in androgen insensitivity syndromeJonathan S Berg, Shannon L French, Laurence B McCullough, et al.
Nature Cell Biology|May 25, 2004
Myosin-X provides a motor-based link between integrins and the cytoskeletonHongquan Zhang, Jonathan S Berg, Zhilun Li, et al.
Personalized Medicine|March 4, 2020
Assessing the implications of positive genomic screening resultsMargaret Waltz, Karen M Meagher, Gail E Henderson, et al.
American Journal of Human Genetics|September 6, 2024
Implementation of a dyadic nomenclature for monogenic diseasesCourtney Thaxton, Leslie G Biesecker, Marina DiStefano, et al.
Cell Genomics|June 27, 2022
Lumping versus splitting: How to approach defining a disease to enable accurate genomic curationCourtney Thaxton, Jennifer Goldstein, Marina DiStefano, et al.
MDM Policy & Practice|June 22, 2018
Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision Making Research in Genomic SequencingMichelle M Langer, Myra I Roche, Noel T Brewer, et al.
Prenatal Diagnosis|July 15, 2021
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fractionDayne L Filer, Piotr A Mieczkowski, Alicia Brandt, et al.
Pediatrics|January 6, 2016
Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision AidMegan A Lewis, Ryan S Paquin, Myra I Roche, et al.
Pageof 17

Showing results (41-50 of 168) with videos related to

Sort By:
Pageof 17
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2012
An informatics approach to analyzing the incidentalomeJonathan S Berg, Michael Adams, Nassib Nassar, et al.
Genome Medicine|December 1, 2019
Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert PanelsDona M Kanavy, Shannon M McNulty, Meera K Jairath, et al.
The Journal of Pediatrics|March 27, 2007
Ethical and legal implications of genetic testing in androgen insensitivity syndromeJonathan S Berg, Shannon L French, Laurence B McCullough, et al.
Nature Cell Biology|May 25, 2004
Myosin-X provides a motor-based link between integrins and the cytoskeletonHongquan Zhang, Jonathan S Berg, Zhilun Li, et al.
Personalized Medicine|March 4, 2020
Assessing the implications of positive genomic screening resultsMargaret Waltz, Karen M Meagher, Gail E Henderson, et al.
American Journal of Human Genetics|September 6, 2024
Implementation of a dyadic nomenclature for monogenic diseasesCourtney Thaxton, Leslie G Biesecker, Marina DiStefano, et al.
Cell Genomics|June 27, 2022
Lumping versus splitting: How to approach defining a disease to enable accurate genomic curationCourtney Thaxton, Jennifer Goldstein, Marina DiStefano, et al.
MDM Policy & Practice|June 22, 2018
Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision Making Research in Genomic SequencingMichelle M Langer, Myra I Roche, Noel T Brewer, et al.
Prenatal Diagnosis|July 15, 2021
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fractionDayne L Filer, Piotr A Mieczkowski, Alicia Brandt, et al.
Pediatrics|January 6, 2016
Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision AidMegan A Lewis, Ryan S Paquin, Myra I Roche, et al.
Pageof 17