Search research articles
Contact Us
Filters
Showing results (351-360 of 590) with videos related to
Page
of 59
Sort By:
Plos One
|
June 1, 2011
A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample
Ma'en Obeidat, Louise V Wain, Nick Shrine, et al.
Plos Genetics
|
December 17, 2009
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
J Brent Richards, Dawn Waterworth, Stephen O'Rahilly, et al.
Nature Methods
|
December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
Eric Van Buren, Yi Zhang, Xihao Li, et al.
Nature Genetics
|
July 18, 2017
Association analyses based on false discovery rate implicate new loci for coronary artery disease
Christopher P Nelson, Anuj Goel, Adam S Butterworth, et al.
Circulation. Genomic and Precision Medicine
|
May 28, 2024
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias
Lu-Chen Weng, Shaan Khurshid, Amelia Weber Hall, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 12, 2025
A Biological-Systems-Based Analyses Using Proteomic and Metabolic Network Inference Reveals Mechanistic Insights into Hepatic Lipid Accumulation: An IMI-DIRECT Study
Natalie N Atabaki, Daniel E Coral, Hugo Pomares-Millan, et al.
International Journal of Epidemiology
|
May 23, 2018
Genetic and environmental factors affecting birth size variation: a pooled individual-based analysis of secular trends and global geographical differences using 26 twin cohorts
Yoshie Yokoyama, Aline Jelenkovic, Yoon-Mi Hur, et al.
Diabetologia
|
May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes
Alicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature Communications
|
October 9, 2024
Rare variant contribution to the heritability of coronary artery disease
Ghislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Human Molecular Genetics
|
September 23, 2021
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Amarise Little, Yao Hu, Quan Sun, et al.
Page
of 59
Search research articles
Search
Showing results (351-360 of 590) with videos related to
Sort By:
Page
of 59
Plos One
|
June 1, 2011
A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample
Ma'en Obeidat, Louise V Wain, Nick Shrine, et al.
Plos Genetics
|
December 17, 2009
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
J Brent Richards, Dawn Waterworth, Stephen O'Rahilly, et al.
Nature Methods
|
December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
Eric Van Buren, Yi Zhang, Xihao Li, et al.
Nature Genetics
|
July 18, 2017
Association analyses based on false discovery rate implicate new loci for coronary artery disease
Christopher P Nelson, Anuj Goel, Adam S Butterworth, et al.
Circulation. Genomic and Precision Medicine
|
May 28, 2024
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias
Lu-Chen Weng, Shaan Khurshid, Amelia Weber Hall, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 12, 2025
A Biological-Systems-Based Analyses Using Proteomic and Metabolic Network Inference Reveals Mechanistic Insights into Hepatic Lipid Accumulation: An IMI-DIRECT Study
Natalie N Atabaki, Daniel E Coral, Hugo Pomares-Millan, et al.
International Journal of Epidemiology
|
May 23, 2018
Genetic and environmental factors affecting birth size variation: a pooled individual-based analysis of secular trends and global geographical differences using 26 twin cohorts
Yoshie Yokoyama, Aline Jelenkovic, Yoon-Mi Hur, et al.
Diabetologia
|
May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes
Alicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature Communications
|
October 9, 2024
Rare variant contribution to the heritability of coronary artery disease
Ghislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Human Molecular Genetics
|
September 23, 2021
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Amarise Little, Yao Hu, Quan Sun, et al.
Page
of 59