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Stacey B Gabriel

Showing results (111-120 of 133) with videos related to

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Plos One|November 1, 2008
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studiesBrendan J Keating, Sam Tischfield, Sarah S Murray, et al.
Nature|November 6, 2007
Characterizing the cancer genome in lung adenocarcinomaBarbara A Weir, Michele S Woo, Gad Getz, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencingAlba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
Medrxiv : the Preprint Server for Health Sciences|October 27, 2021
Evidence of transmission from fully vaccinated individuals in a large outbreak of the SARS-CoV-2 Delta variant in Provincetown, MassachusettsKatherine J Siddle, Lydia A Krasilnikova, Gage K Moreno, et al.
Cell|January 20, 2022
Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreakKatherine J Siddle, Lydia A Krasilnikova, Gage K Moreno, et al.
Nature|October 25, 2008
Somatic mutations affect key pathways in lung adenocarcinomaLi Ding, Gad Getz, David A Wheeler, et al.
Nature|September 3, 2010
Integrating common and rare genetic variation in diverse human populations, David M Altshuler, Richard A Gibbs, et al.
Pageof 14

Showing results (111-120 of 133) with videos related to

Sort By:
Pageof 14
Plos One|November 1, 2008
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studiesBrendan J Keating, Sam Tischfield, Sarah S Murray, et al.
Nature|November 6, 2007
Characterizing the cancer genome in lung adenocarcinomaBarbara A Weir, Michele S Woo, Gad Getz, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencingAlba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
Medrxiv : the Preprint Server for Health Sciences|October 27, 2021
Evidence of transmission from fully vaccinated individuals in a large outbreak of the SARS-CoV-2 Delta variant in Provincetown, MassachusettsKatherine J Siddle, Lydia A Krasilnikova, Gage K Moreno, et al.
Cell|January 20, 2022
Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreakKatherine J Siddle, Lydia A Krasilnikova, Gage K Moreno, et al.
Nature|October 25, 2008
Somatic mutations affect key pathways in lung adenocarcinomaLi Ding, Gad Getz, David A Wheeler, et al.
Nature|September 3, 2010
Integrating common and rare genetic variation in diverse human populations, David M Altshuler, Richard A Gibbs, et al.
Pageof 14