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Nathan O Stitziel

Showing results (71-80 of 92) with videos related to

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Human Molecular Genetics|September 5, 2014
Association of exome sequences with plasma C-reactive protein levels in >9000 participantsUrsula M Schick, Paul L Auer, Joshua C Bis, et al.
JAMA|March 8, 2017
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery DiseaseAmit V Khera, Hong-Hee Won, Gina M Peloso, et al.
Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.
Science (New York, N.Y.)|March 12, 2016
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart diseasePaolo Zanoni, Sumeet A Khetarpal, Daniel B Larach, et al.
Biorxiv : the Preprint Server for Biology|December 31, 2025
Complete genomes of a multi-generational pedigree to expand studies of genetic and epigenetic inheritanceMonika Cechova, Tamara A Potapova, Andreas Rechtsteiner, et al.
Plos Genetics|August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder populationElaine T Lim, Peter Würtz, Aki S Havulinna, et al.
European Journal of Preventive Cardiology|December 13, 2016
Genetic invalidation of Lp-PLA<sub>2</sub> as a therapeutic target: Large-scale study of five functional Lp-PLA<sub>2</sub>-lowering allelesJohn M Gregson, Daniel F Freitag, Praveen Surendran, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|September 5, 2014
Association of exome sequences with plasma C-reactive protein levels in >9000 participantsUrsula M Schick, Paul L Auer, Joshua C Bis, et al.
JAMA|March 8, 2017
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery DiseaseAmit V Khera, Hong-Hee Won, Gina M Peloso, et al.
Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.
Science (New York, N.Y.)|March 12, 2016
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart diseasePaolo Zanoni, Sumeet A Khetarpal, Daniel B Larach, et al.
Biorxiv : the Preprint Server for Biology|December 31, 2025
Complete genomes of a multi-generational pedigree to expand studies of genetic and epigenetic inheritanceMonika Cechova, Tamara A Potapova, Andreas Rechtsteiner, et al.
Plos Genetics|August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder populationElaine T Lim, Peter Würtz, Aki S Havulinna, et al.
European Journal of Preventive Cardiology|December 13, 2016
Genetic invalidation of Lp-PLA<sub>2</sub> as a therapeutic target: Large-scale study of five functional Lp-PLA<sub>2</sub>-lowering allelesJohn M Gregson, Daniel F Freitag, Praveen Surendran, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Pageof 10