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Eric Boerwinkle

Showing results (931-940 of 1,171) with videos related to

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Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Annals of Neurology|June 18, 2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortiumMyriam Fornage, Stephanie Debette, Joshua C Bis, et al.
Plos Genetics|July 9, 2011
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individualsDan E Arking, M Juhani Junttila, Philippe Goyette, et al.
Plos Genetics|June 27, 2009
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE ConsortiumNancy L Heard-Costa, M Carola Zillikens, Keri L Monda, et al.
Plos Genetics|February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe ProjectGuillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Genetics|December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studiesXihao Li, Corbin Quick, Hufeng Zhou, et al.
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.
Circulation|December 7, 2011
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarctionChristopher J O'Donnell, Maryam Kavousi, Albert V Smith, et al.
Plos One|March 8, 2016
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE ConsortiumAbbas Dehghan, Joshua C Bis, Charles C White, 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 118

Showing results (931-940 of 1,171) with videos related to

Sort By:
Pageof 118
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Annals of Neurology|June 18, 2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortiumMyriam Fornage, Stephanie Debette, Joshua C Bis, et al.
Plos Genetics|July 9, 2011
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individualsDan E Arking, M Juhani Junttila, Philippe Goyette, et al.
Plos Genetics|June 27, 2009
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE ConsortiumNancy L Heard-Costa, M Carola Zillikens, Keri L Monda, et al.
Plos Genetics|February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe ProjectGuillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Genetics|December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studiesXihao Li, Corbin Quick, Hufeng Zhou, et al.
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.
Circulation|December 7, 2011
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarctionChristopher J O'Donnell, Maryam Kavousi, Albert V Smith, et al.
Plos One|March 8, 2016
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE ConsortiumAbbas Dehghan, Joshua C Bis, Charles C White, 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 118