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V Khera

Showing results (121-130 of 140) with videos related to

Pageof 14
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Nature|March 11, 2021
Improving reporting standards for polygenic scores in risk prediction studiesHannah Wand, Samuel A Lambert, Cecelia Tamburro, et al.
Nature Communications|August 25, 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individualsPradeep Natarajan, Gina M Peloso, Seyedeh Maryam Zekavat, et al.
Obesity (Silver Spring, Md.)|November 13, 2022
Quantifying the phenome-wide disease burden of obesity using electronic health records and genomicsJamie R Robinson, Robert J Carroll, Lisa Bastarache, et al.
JAMA Cardiology|January 31, 2024
Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated CholesterolYiyi Zhang, Jacqueline S Dron, Brandon K Bellows, 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.
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 Genetics|October 3, 2018
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran ProgramDerek Klarin, Scott M Damrauer, Kelly Cho, et al.
Nature|May 29, 2020
A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Circulation Research|May 17, 2017
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart DiseaseAkihiro Nomura, Hong-Hee Won, Amit V Khera, et al.
Nature Communications|June 8, 2023
South Asian medical cohorts reveal strong founder effects and high rates of homozygosityJeffrey D Wall, J Fah Sathirapongsasuti, Ravi Gupta, et al.
Pageof 14

Showing results (121-130 of 140) with videos related to

Sort By:
Pageof 14
Nature|March 11, 2021
Improving reporting standards for polygenic scores in risk prediction studiesHannah Wand, Samuel A Lambert, Cecelia Tamburro, et al.
Nature Communications|August 25, 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individualsPradeep Natarajan, Gina M Peloso, Seyedeh Maryam Zekavat, et al.
Obesity (Silver Spring, Md.)|November 13, 2022
Quantifying the phenome-wide disease burden of obesity using electronic health records and genomicsJamie R Robinson, Robert J Carroll, Lisa Bastarache, et al.
JAMA Cardiology|January 31, 2024
Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated CholesterolYiyi Zhang, Jacqueline S Dron, Brandon K Bellows, 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.
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 Genetics|October 3, 2018
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran ProgramDerek Klarin, Scott M Damrauer, Kelly Cho, et al.
Nature|May 29, 2020
A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Circulation Research|May 17, 2017
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart DiseaseAkihiro Nomura, Hong-Hee Won, Amit V Khera, et al.
Nature Communications|June 8, 2023
South Asian medical cohorts reveal strong founder effects and high rates of homozygosityJeffrey D Wall, J Fah Sathirapongsasuti, Ravi Gupta, et al.
Pageof 14