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HGG Advances
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May 24, 2025
Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variants
Samantha J Klasfeld, Katherine A Knutson, Melissa R Miller, et al.
Nucleic Acids Research
|
September 22, 2018
ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci
David Stacey, Eric B Fauman, Daniel Ziemek, et al.
Genome Biology
|
February 3, 2025
Multi-INTACT: integrative analysis of the genome, transcriptome, and proteome identifies causal mechanisms of complex traits
Jeffrey Okamoto, Xianyong Yin, Brady Ryan, et al.
Human Molecular Genetics
|
February 16, 2017
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci
Amy V Jones, Mera Tilley, Alex Gutteridge, et al.
Nature Genetics
|
October 29, 2021
An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci
Edward Mountjoy, Ellen M Schmidt, Miguel Carmona, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 10, 2023
Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health
Xianyong Yin, Jack Li, Debraj Bose, et al.
Elife
|
March 18, 2022
Effector membrane translocation biosensors reveal G protein and βarrestin coupling profiles of 100 therapeutically relevant GPCRs
Charlotte Avet, Arturo Mancini, Billy Breton, et al.
Research Square
|
January 16, 2026
Ratio-Driven Lipoprotein Mapping Refines Genetic Pathways of Cardiometabolic Risk
S Hani Najafi-Shoushtari, Karsten Suhre, Murugan Subramanian, et al.
Nature Communications
|
March 29, 2025
Assessing the potential causal effects of 1099 plasma metabolites on 2099 binary disease endpoints
Xianyong Yin, Jack Li, Debraj Bose, et al.
Elife
|
March 25, 2020
Characterising a healthy adult with a rare HAO1 knockout to support a therapeutic strategy for primary hyperoxaluria
Tracy L McGregor, Karen A Hunt, Elaine Yee, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
HGG Advances
|
May 24, 2025
Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variants
Samantha J Klasfeld, Katherine A Knutson, Melissa R Miller, et al.
Nucleic Acids Research
|
September 22, 2018
ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci
David Stacey, Eric B Fauman, Daniel Ziemek, et al.
Genome Biology
|
February 3, 2025
Multi-INTACT: integrative analysis of the genome, transcriptome, and proteome identifies causal mechanisms of complex traits
Jeffrey Okamoto, Xianyong Yin, Brady Ryan, et al.
Human Molecular Genetics
|
February 16, 2017
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci
Amy V Jones, Mera Tilley, Alex Gutteridge, et al.
Nature Genetics
|
October 29, 2021
An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci
Edward Mountjoy, Ellen M Schmidt, Miguel Carmona, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 10, 2023
Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health
Xianyong Yin, Jack Li, Debraj Bose, et al.
Elife
|
March 18, 2022
Effector membrane translocation biosensors reveal G protein and βarrestin coupling profiles of 100 therapeutically relevant GPCRs
Charlotte Avet, Arturo Mancini, Billy Breton, et al.
Research Square
|
January 16, 2026
Ratio-Driven Lipoprotein Mapping Refines Genetic Pathways of Cardiometabolic Risk
S Hani Najafi-Shoushtari, Karsten Suhre, Murugan Subramanian, et al.
Nature Communications
|
March 29, 2025
Assessing the potential causal effects of 1099 plasma metabolites on 2099 binary disease endpoints
Xianyong Yin, Jack Li, Debraj Bose, et al.
Elife
|
March 25, 2020
Characterising a healthy adult with a rare HAO1 knockout to support a therapeutic strategy for primary hyperoxaluria
Tracy L McGregor, Karen A Hunt, Elaine Yee, et al.
Page
of 4