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Lisa R Yanek

Showing results (141-150 of 245) with videos related to

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Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
Communications Biology|August 10, 2019
A genome-wide association study identifies genetic loci associated with specific lobar brain volumesSven J van der Lee, Maria J Knol, Ganesh Chauhan, et al.
Atherosclerosis|February 25, 2012
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortiumChristina L Wassel, Claudia Lamina, Vijay Nambi, et al.
Nature Communications|October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with heightGareth Hawkes, Robin N Beaumont, Zilin Li, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Plos One|May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart diseaseCavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, 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.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Circulation. Genomic and Precision Medicine|November 28, 2023
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical AtherosclerosisNatalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Pageof 25

Showing results (141-150 of 245) with videos related to

Sort By:
Pageof 25
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
Communications Biology|August 10, 2019
A genome-wide association study identifies genetic loci associated with specific lobar brain volumesSven J van der Lee, Maria J Knol, Ganesh Chauhan, et al.
Atherosclerosis|February 25, 2012
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortiumChristina L Wassel, Claudia Lamina, Vijay Nambi, et al.
Nature Communications|October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with heightGareth Hawkes, Robin N Beaumont, Zilin Li, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Plos One|May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart diseaseCavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, 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.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Circulation. Genomic and Precision Medicine|November 28, 2023
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical AtherosclerosisNatalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Pageof 25