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Nature Human Behaviour
|
August 4, 2022
Rare genetic variants explain missing heritability in smoking
Seon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
Clinical Epigenetics
|
September 11, 2023
Analysis of DNA methylation at birth and in childhood reveals changes associated with season of birth and latitude
Latha Kadalayil, Md Zahangir Alam, Cory Haley White, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 5, 2026
Idiopathic Pulmonary Fibrosis Risk Loci in East Asian Populations Mirror those of European Populations
Anna L Peljto, Haruhiko Furusawa, Deepa Puthenvedu, 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.
American Journal of Respiratory and Critical Care Medicine
|
January 5, 2023
Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants
Anna L Peljto, Rachel Z Blumhagen, Avram D Walts, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 30, 2019
Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis
Camille Moore, Rachel Z Blumhagen, Ivana V Yang, et al.
Nature Communications
|
April 25, 2019
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight
Leanne K Küpers, Claire Monnereau, Gemma C Sharp, et al.
International Journal of Epidemiology
|
October 13, 2017
Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium
Janine F Felix, Bonnie R Joubert, Andrea A Baccarelli, et al.
Nature
|
October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Nature
|
March 12, 2021
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
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of 35
Search research articles
Search
Showing results (331-340 of 342) with videos related to
Sort By:
Page
of 35
Nature Human Behaviour
|
August 4, 2022
Rare genetic variants explain missing heritability in smoking
Seon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
Clinical Epigenetics
|
September 11, 2023
Analysis of DNA methylation at birth and in childhood reveals changes associated with season of birth and latitude
Latha Kadalayil, Md Zahangir Alam, Cory Haley White, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 5, 2026
Idiopathic Pulmonary Fibrosis Risk Loci in East Asian Populations Mirror those of European Populations
Anna L Peljto, Haruhiko Furusawa, Deepa Puthenvedu, 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.
American Journal of Respiratory and Critical Care Medicine
|
January 5, 2023
Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants
Anna L Peljto, Rachel Z Blumhagen, Avram D Walts, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 30, 2019
Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis
Camille Moore, Rachel Z Blumhagen, Ivana V Yang, et al.
Nature Communications
|
April 25, 2019
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight
Leanne K Küpers, Claire Monnereau, Gemma C Sharp, et al.
International Journal of Epidemiology
|
October 13, 2017
Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium
Janine F Felix, Bonnie R Joubert, Andrea A Baccarelli, et al.
Nature
|
October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Nature
|
March 12, 2021
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Alexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Page
of 35