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Human Molecular Genetics
|
September 1, 2016
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Daniel S Evans, Christy L Avery, Mike A Nalls, 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 Project
Guillaume Lettre, Cameron D Palmer, Taylor Young, 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) consortium
Christina L Wassel, Claudia Lamina, Vijay Nambi, et al.
Plos One
|
December 14, 2012
Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations
Clara C Elbers, Yiran Guo, Vinicius Tragante, et al.
Nature
|
July 22, 2011
The landscape of recombination in African Americans
Anjali G Hinch, Arti Tandon, Nick Patterson, et al.
Plos Genetics
|
August 8, 2014
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes
Maggie C Y Ng, Daniel Shriner, Brian H Chen, et al.
Nature
|
December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do, Nathan O Stitziel, Hong-Hee Won, et al.
Journal of the American Society of Nephrology : JASN
|
April 1, 2017
<i>NFAT5</i> and <i>SLC4A10</i> Loci Associate with Plasma Osmolality
Carsten A Böger, Mathias Gorski, Gearoid M McMahon, et al.
American Journal of Human Genetics
|
February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
Gina M Peloso, Paul L Auer, Joshua C Bis, et al.
American Journal of Human Genetics
|
February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
Leslie A Lange, Youna Hu, He Zhang, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 198) with videos related to
Sort By:
Page
of 20
Human Molecular Genetics
|
September 1, 2016
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Daniel S Evans, Christy L Avery, Mike A Nalls, 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 Project
Guillaume Lettre, Cameron D Palmer, Taylor Young, 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) consortium
Christina L Wassel, Claudia Lamina, Vijay Nambi, et al.
Plos One
|
December 14, 2012
Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations
Clara C Elbers, Yiran Guo, Vinicius Tragante, et al.
Nature
|
July 22, 2011
The landscape of recombination in African Americans
Anjali G Hinch, Arti Tandon, Nick Patterson, et al.
Plos Genetics
|
August 8, 2014
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes
Maggie C Y Ng, Daniel Shriner, Brian H Chen, et al.
Nature
|
December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do, Nathan O Stitziel, Hong-Hee Won, et al.
Journal of the American Society of Nephrology : JASN
|
April 1, 2017
<i>NFAT5</i> and <i>SLC4A10</i> Loci Associate with Plasma Osmolality
Carsten A Böger, Mathias Gorski, Gearoid M McMahon, et al.
American Journal of Human Genetics
|
February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
Gina M Peloso, Paul L Auer, Joshua C Bis, et al.
American Journal of Human Genetics
|
February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
Leslie A Lange, Youna Hu, He Zhang, et al.
Page
of 20