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Dan-Yu Lin

Showing results (81-90 of 93) with videos related to

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Frontiers in Genetics|June 11, 2019
Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE StudyBridget M Lin, Girish N Nadkarni, Ran Tao, et al.
American Journal of Human Genetics|October 1, 2019
Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic TraitsChelsea K Raulerson, Arthur Ko, John C Kidd, et al.
Plos One|December 27, 2014
Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE studyNora Franceschini, Yijuan Hu, Alex P Reiner, et al.
Heart Rhythm|December 19, 2016
Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populationsChristy L Avery, Christina L Wassel, Melissa A Richard, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature|June 21, 2019
Genetic analyses of diverse populations improves discovery for complex traitsGenevieve L Wojcik, Mariaelisa Graff, Katherine K Nishimura, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Frontiers in Genetics|June 11, 2019
Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE StudyBridget M Lin, Girish N Nadkarni, Ran Tao, et al.
American Journal of Human Genetics|October 1, 2019
Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic TraitsChelsea K Raulerson, Arthur Ko, John C Kidd, et al.
Plos One|December 27, 2014
Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE studyNora Franceschini, Yijuan Hu, Alex P Reiner, et al.
Heart Rhythm|December 19, 2016
Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populationsChristy L Avery, Christina L Wassel, Melissa A Richard, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature|June 21, 2019
Genetic analyses of diverse populations improves discovery for complex traitsGenevieve L Wojcik, Mariaelisa Graff, Katherine K Nishimura, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Pageof 10