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American Journal of Human Genetics
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June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases
Salman M Tajuddin, Ursula M Schick, John D Eicher, 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 Genetics
|
December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Aeron M Small, Ta-Yu Yang, Shinsuke Itoh, et al.
Nature Communications
|
October 1, 2017
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits
Aurélien Macé, Marcus A Tuke, Patrick Deelen, 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.
Nature Communications
|
April 2, 2020
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Jingyuan Xie, Lili Liu, Nikol Mladkova, 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.
Diabetes
|
March 15, 2012
No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels
Robert A Scott, Audrey Y Chu, Niels Grarup, et al.
American Journal of Human Genetics
|
June 11, 2019
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Cassandra N Spracklen, Tugce Karaderi, Hanieh Yaghootkar, et al.
Nature Genetics
|
December 9, 2008
Variants in MTNR1B influence fasting glucose levels
Inga Prokopenko, Claudia Langenberg, Jose C Florez, et al.
Page
of 59
Search research articles
Search
Showing results (431-440 of 590) with videos related to
Sort By:
Page
of 59
American Journal of Human Genetics
|
June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases
Salman M Tajuddin, Ursula M Schick, John D Eicher, 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 Genetics
|
December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Aeron M Small, Ta-Yu Yang, Shinsuke Itoh, et al.
Nature Communications
|
October 1, 2017
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits
Aurélien Macé, Marcus A Tuke, Patrick Deelen, 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.
Nature Communications
|
April 2, 2020
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Jingyuan Xie, Lili Liu, Nikol Mladkova, 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.
Diabetes
|
March 15, 2012
No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels
Robert A Scott, Audrey Y Chu, Niels Grarup, et al.
American Journal of Human Genetics
|
June 11, 2019
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Cassandra N Spracklen, Tugce Karaderi, Hanieh Yaghootkar, et al.
Nature Genetics
|
December 9, 2008
Variants in MTNR1B influence fasting glucose levels
Inga Prokopenko, Claudia Langenberg, Jose C Florez, et al.
Page
of 59