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David B Goldstein

Showing results (301-310 of 338) with videos related to

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JAMA Network Open|March 11, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 11, 2015
Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus loadPaul J McLaren, Cedric Coulonges, István Bartha, et al.
American Journal of Human Genetics|September 8, 2018
IRF2BPL Is Associated with Neurological PhenotypesPaul C Marcogliese, Vandana Shashi, Rebecca C Spillmann, et al.
Nature|June 21, 2019
Noncoding deletions reveal a gene that is critical for intestinal functionDanit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
Brain : a Journal of Neurology|June 5, 2010
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association studyDalia Kasperaviciūte, Claudia B Catarino, Erin L Heinzen, et al.
Medrxiv : the Preprint Server for Health Sciences|January 5, 2021
Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
The New England Journal of Medicine|June 18, 2015
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive InfectionsKerry Dobbs, Cecilia Domínguez Conde, Shen-Ying Zhang, et al.
Patterns (New York, N.Y.)|August 29, 2022
The <i>All of Us</i> Research Program: Data quality, utility, and diversityAndrea H Ramirez, Lina Sulieman, David J Schlueter, et al.
Pageof 34

Showing results (301-310 of 338) with videos related to

Sort By:
Pageof 34
JAMA Network Open|March 11, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 11, 2015
Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus loadPaul J McLaren, Cedric Coulonges, István Bartha, et al.
American Journal of Human Genetics|September 8, 2018
IRF2BPL Is Associated with Neurological PhenotypesPaul C Marcogliese, Vandana Shashi, Rebecca C Spillmann, et al.
Nature|June 21, 2019
Noncoding deletions reveal a gene that is critical for intestinal functionDanit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
Brain : a Journal of Neurology|June 5, 2010
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association studyDalia Kasperaviciūte, Claudia B Catarino, Erin L Heinzen, et al.
Medrxiv : the Preprint Server for Health Sciences|January 5, 2021
Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
The New England Journal of Medicine|June 18, 2015
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive InfectionsKerry Dobbs, Cecilia Domínguez Conde, Shen-Ying Zhang, et al.
Patterns (New York, N.Y.)|August 29, 2022
The <i>All of Us</i> Research Program: Data quality, utility, and diversityAndrea H Ramirez, Lina Sulieman, David J Schlueter, et al.
Pageof 34