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Nature Genetics
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March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Cell
|
September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Circulation. Cardiovascular Genetics
|
November 23, 2016
Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis
Pradeep Natarajan, Joshua C Bis, Lawrence F Bielak, et al.
Nature Communications
|
May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Rebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Genome Biology
|
June 30, 2021
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Daniel L McCartney, Josine L Min, Rebecca C Richmond, et al.
American Journal of Human Genetics
|
June 28, 2016
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits
Nathalie Chami, Ming-Huei Chen, Andrew J Slater, et al.
Nature
|
April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
Joshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.
American Journal of Human Genetics
|
June 28, 2016
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals
John D Eicher, Nathalie Chami, Tim Kacprowski, et al.
Science Advances
|
April 6, 2022
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Tetsushi Nakao, Alexander G Bick, Margaret A Taub, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2026
<i>Trans</i> -eQTLs reveal the architecture of human gene regulatory networks
C A Robert Warmerdam, Harm-Jan Westra, Adriaan van der Graaf, et al.
Page
of 27
Search research articles
Search
Showing results (231-240 of 269) with videos related to
Sort By:
Page
of 27
Nature Genetics
|
March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Cell
|
September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Circulation. Cardiovascular Genetics
|
November 23, 2016
Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis
Pradeep Natarajan, Joshua C Bis, Lawrence F Bielak, et al.
Nature Communications
|
May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Rebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Genome Biology
|
June 30, 2021
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Daniel L McCartney, Josine L Min, Rebecca C Richmond, et al.
American Journal of Human Genetics
|
June 28, 2016
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits
Nathalie Chami, Ming-Huei Chen, Andrew J Slater, et al.
Nature
|
April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
Joshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.
American Journal of Human Genetics
|
June 28, 2016
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals
John D Eicher, Nathalie Chami, Tim Kacprowski, et al.
Science Advances
|
April 6, 2022
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Tetsushi Nakao, Alexander G Bick, Margaret A Taub, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2026
<i>Trans</i> -eQTLs reveal the architecture of human gene regulatory networks
C A Robert Warmerdam, Harm-Jan Westra, Adriaan van der Graaf, et al.
Page
of 27