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Stacey Gabriel

Showing results (121-130 of 195) with videos related to

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European Journal of Human Genetics : EJHG|January 14, 2016
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing ProjectMengyuan Kan, Paul L Auer, Gao T Wang, et al.
Journal of the American College of Cardiology|April 7, 2016
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe HypercholesterolemiaAmit V Khera, Hong-Hee Won, Gina M Peloso, et al.
Cell Genomics|October 23, 2023
The functional impact of rare variation across the regulatory cascadeTaibo Li, Nicole Ferraro, Benjamin J Strober, et al.
Nature|July 6, 2017
An immunogenic personal neoantigen vaccine for patients with melanomaPatrick A Ott, Zhuting Hu, Derin B Keskin, et al.
Nature Genetics|February 12, 2013
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.
Nature Communications|May 21, 2016
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibitionJan A Burger, Dan A Landau, Amaro Taylor-Weiner, et al.
Nature|March 16, 2018
Corrigendum: An immunogenic personal neoantigen vaccine for patients with melanomaPatrick A Ott, Zhuting Hu, Derin B Keskin, et al.
Nature Genetics|October 28, 2017
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiologyJennifer A Brody, Alanna C Morrison, Joshua C Bis, et al.
Nature Communications|April 26, 2018
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for diseaseConnor A Emdin, Amit V Khera, Mark Chaffin, et al.
Circulation. Cardiovascular Genetics|January 30, 2015
Exome sequencing in suspected monogenic dyslipidemiasNathan O Stitziel, Gina M Peloso, Marianne Abifadel, et al.
Pageof 20

Showing results (121-130 of 195) with videos related to

Sort By:
Pageof 20
European Journal of Human Genetics : EJHG|January 14, 2016
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing ProjectMengyuan Kan, Paul L Auer, Gao T Wang, et al.
Journal of the American College of Cardiology|April 7, 2016
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe HypercholesterolemiaAmit V Khera, Hong-Hee Won, Gina M Peloso, et al.
Cell Genomics|October 23, 2023
The functional impact of rare variation across the regulatory cascadeTaibo Li, Nicole Ferraro, Benjamin J Strober, et al.
Nature|July 6, 2017
An immunogenic personal neoantigen vaccine for patients with melanomaPatrick A Ott, Zhuting Hu, Derin B Keskin, et al.
Nature Genetics|February 12, 2013
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.
Nature Communications|May 21, 2016
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibitionJan A Burger, Dan A Landau, Amaro Taylor-Weiner, et al.
Nature|March 16, 2018
Corrigendum: An immunogenic personal neoantigen vaccine for patients with melanomaPatrick A Ott, Zhuting Hu, Derin B Keskin, et al.
Nature Genetics|October 28, 2017
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiologyJennifer A Brody, Alanna C Morrison, Joshua C Bis, et al.
Nature Communications|April 26, 2018
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for diseaseConnor A Emdin, Amit V Khera, Mark Chaffin, et al.
Circulation. Cardiovascular Genetics|January 30, 2015
Exome sequencing in suspected monogenic dyslipidemiasNathan O Stitziel, Gina M Peloso, Marianne Abifadel, et al.
Pageof 20