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Ron Do

Showing results (121-130 of 172) with videos related to

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The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
JAMA|October 27, 2014
Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosisJ Gustav Smith, Kevin Luk, Christina-Alexandra Schulz, et al.
Genome Biology|January 27, 2021
Exploiting the GTEx resources to decipher the mechanisms at GWAS lociAlvaro N Barbeira, Rodrigo Bonazzola, Eric R Gamazon, et al.
Journal of the American College of Cardiology|June 6, 2020
Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery DiseaseKrishna G Aragam, Amanda Dobbyn, Renae Judy, et al.
JAMA|December 11, 2019
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino AncestryScott M Damrauer, Kumardeep Chaudhary, Judy H Cho, et al.
American Journal of Human Genetics|October 3, 2015
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk ScoresBjarni J Vilhjálmsson, Jian Yang, Hilary K Finucane, et al.
Science (New York, N.Y.)|September 1, 2012
A high-coverage genome sequence from an archaic Denisovan individualMatthias Meyer, Martin Kircher, Marie-Theres Gansauge, et al.
Nature Medicine|May 29, 2023
Polygenic prediction of preeclampsia and gestational hypertensionMichael C Honigberg, Buu Truong, Raiyan R Khan, et al.
Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Pageof 18

Showing results (121-130 of 172) with videos related to

Sort By:
Pageof 18
The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
JAMA|October 27, 2014
Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosisJ Gustav Smith, Kevin Luk, Christina-Alexandra Schulz, et al.
Genome Biology|January 27, 2021
Exploiting the GTEx resources to decipher the mechanisms at GWAS lociAlvaro N Barbeira, Rodrigo Bonazzola, Eric R Gamazon, et al.
Journal of the American College of Cardiology|June 6, 2020
Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery DiseaseKrishna G Aragam, Amanda Dobbyn, Renae Judy, et al.
JAMA|December 11, 2019
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino AncestryScott M Damrauer, Kumardeep Chaudhary, Judy H Cho, et al.
American Journal of Human Genetics|October 3, 2015
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk ScoresBjarni J Vilhjálmsson, Jian Yang, Hilary K Finucane, et al.
Science (New York, N.Y.)|September 1, 2012
A high-coverage genome sequence from an archaic Denisovan individualMatthias Meyer, Martin Kircher, Marie-Theres Gansauge, et al.
Nature Medicine|May 29, 2023
Polygenic prediction of preeclampsia and gestational hypertensionMichael C Honigberg, Buu Truong, Raiyan R Khan, et al.
Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Pageof 18