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Lista de obras de Hugues Aschard

A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context

artículo científico publicado en 2019

A test for gene-environment interaction in the presence of measurement error in the environmental variable.

artículo científico publicado en 2018

Adjusting for Principal Components of Molecular Phenotypes Induces Replicating False Positives

scientific article published on 28 January 2019

An ancestry-based approach for detecting interactions

artículo científico publicado en 2017

Covariate selection for association screening in multiphenotype genetic studies

artículo científico publicado en 2017

Estimating the effective sample size in association studies of quantitative traits

artículo científico publicado en 2021

Exploring the Genetic Basis of Human Population Differences in DNA Methylation and their Causal Impact on Immune Gene Regulation

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

Genetic effects on the commensal microbiota in inflammatory bowel disease patients

artículo científico publicado en 2019

JASS: command line and web interface for the joint analysis of GWAS results

artículo científico publicado en 2020

Joint Analysis of Multiple Interaction Parameters in Genetic Association Studies

artículo científico publicado en 2018

Making the Most of Clumping and Thresholding for Polygenic Scores

scientific article published on 21 November 2019

Mixed-model admixture mapping identifies smoking-dependent loci of lung function in African Americans

scientific article published on 13 December 2019

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

artículo científico publicado en 2019

Multitrait GWAS to connect disease variants and biological mechanisms

artículo científico publicado en 2021

Screening for interaction effects in gene expression data

artículo científico publicado en 2017

Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis

scientific article published on 23 November 2020