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Nature Genetics
|
August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Nature Communications
|
October 27, 2015
Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci
Fredrick R Schumacher, Stephanie L Schmit, Shuo Jiao, et al.
Circulation. Genomic and Precision Medicine
|
May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval
Honghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Human Behaviour
|
August 4, 2022
Rare genetic variants explain missing heritability in smoking
Seon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
Nature Communications
|
July 8, 2015
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Fredrick R Schumacher, Stephanie L Schmit, Shuo Jiao, et al.
Communications Biology
|
July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program
Daniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Blood
|
February 6, 2024
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels
Paul S de Vries, Paula Reventun, Michael R Brown, 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.
Journal of the National Cancer Institute
|
December 13, 2018
Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer
Naomi Walsh, Han Zhang, Paula L Hyland, et al.
Nature Genetics
|
January 26, 2023
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing
Fang Chen, Xingyan Wang, Seon-Kyeong Jang, et al.
Page
of 53
Search research articles
Search
Showing results (431-440 of 530) with videos related to
Sort By:
Page
of 53
Nature Genetics
|
August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Nature Communications
|
October 27, 2015
Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci
Fredrick R Schumacher, Stephanie L Schmit, Shuo Jiao, et al.
Circulation. Genomic and Precision Medicine
|
May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval
Honghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Human Behaviour
|
August 4, 2022
Rare genetic variants explain missing heritability in smoking
Seon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
Nature Communications
|
July 8, 2015
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Fredrick R Schumacher, Stephanie L Schmit, Shuo Jiao, et al.
Communications Biology
|
July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program
Daniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Blood
|
February 6, 2024
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels
Paul S de Vries, Paula Reventun, Michael R Brown, 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.
Journal of the National Cancer Institute
|
December 13, 2018
Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer
Naomi Walsh, Han Zhang, Paula L Hyland, et al.
Nature Genetics
|
January 26, 2023
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing
Fang Chen, Xingyan Wang, Seon-Kyeong Jang, et al.
Page
of 53