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Showing results (261-270 of 347) with videos related to

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The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Genetic Epidemiology|August 19, 2010
Quality control and quality assurance in genotypic data for genome-wide association studiesCathy C Laurie, Kimberly F Doheny, Daniel B Mirel, et al.
Neurology. Genetics|November 30, 2017
The Alzheimer's Disease Sequencing Project: Study design and sample selectionGary W Beecham, J C Bis, E R Martin, et al.
Nature Genetics|September 9, 2008
Integrated detection and population-genetic analysis of SNPs and copy number variationSteven A McCarroll, Finny G Kuruvilla, Joshua M Korn, et al.
American Journal of Human Genetics|September 11, 2012
Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohortsAlexander G Bick, Jason Flannick, Kaoru Ito, et al.
Cancer Discovery|November 23, 2013
MAP kinase pathway alterations in BRAF-mutant melanoma patients with acquired resistance to combined RAF/MEK inhibitionNikhil Wagle, Eliezer M Van Allen, Daniel J Treacy, et al.
Nature Genetics|August 4, 2014
A framework for the interpretation of de novo mutation in human diseaseKaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.
Plos Genetics|May 22, 2023
Canonical correlation analysis for multi-omics: Application to cross-cohort analysisMin-Zhi Jiang, François Aguet, Kristin Ardlie, et al.
Plos One|May 26, 2012
Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe projectKiran Musunuru, Simon P R Romaine, Guillaume Lettre, et al.
American Journal of Human Genetics|February 18, 2010
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 geneEveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, et al.
Pageof 35

Showing results (261-270 of 347) with videos related to

Sort By:
Pageof 35
The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Genetic Epidemiology|August 19, 2010
Quality control and quality assurance in genotypic data for genome-wide association studiesCathy C Laurie, Kimberly F Doheny, Daniel B Mirel, et al.
Neurology. Genetics|November 30, 2017
The Alzheimer's Disease Sequencing Project: Study design and sample selectionGary W Beecham, J C Bis, E R Martin, et al.
Nature Genetics|September 9, 2008
Integrated detection and population-genetic analysis of SNPs and copy number variationSteven A McCarroll, Finny G Kuruvilla, Joshua M Korn, et al.
American Journal of Human Genetics|September 11, 2012
Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohortsAlexander G Bick, Jason Flannick, Kaoru Ito, et al.
Cancer Discovery|November 23, 2013
MAP kinase pathway alterations in BRAF-mutant melanoma patients with acquired resistance to combined RAF/MEK inhibitionNikhil Wagle, Eliezer M Van Allen, Daniel J Treacy, et al.
Nature Genetics|August 4, 2014
A framework for the interpretation of de novo mutation in human diseaseKaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.
Plos Genetics|May 22, 2023
Canonical correlation analysis for multi-omics: Application to cross-cohort analysisMin-Zhi Jiang, François Aguet, Kristin Ardlie, et al.
Plos One|May 26, 2012
Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe projectKiran Musunuru, Simon P R Romaine, Guillaume Lettre, et al.
American Journal of Human Genetics|February 18, 2010
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 geneEveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, et al.
Pageof 35