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Lista de obras de Thibaud S Boutin

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

scientific article published on 29 July 2019

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

artículo científico publicado en 2020

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

artículo científico publicado en 2018

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

artículo científico publicado en 2017

Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants

scientific article published on 11 December 2020

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genome-Wide Meta-Analyses Of Stratified Depression In Generation Scotland And UK Biobank

article

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder

artículo científico publicado en 2016

Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.

artículo científico publicado en 2018

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

artículo científico publicado en 2017

Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level.

artículo científico publicado en 2018

Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

artículo científico publicado en 2016

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

artículo científico publicado en 2017

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

artículo científico publicado en 2020

How does selfing affect the dynamics of selfish transposable elements?

artículo científico publicado en 2012

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

artículo científico publicado en 2020

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

Multi-trait genome-wide association study identifies new loci associated with optic disc parameters

scientific article published on 27 November 2019

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

artículo científico publicado en 2017

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

The Stratification Of Major Depressive Disorder Into Genetic Subgroups

scholarly article published 5 May 2017

The struggle for life of the genome's selfish architects

artículo científico publicado en 2011

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

scientific article published on 21 December 2018

Variants associated with expression have sex-differential effects on lung function

artículo científico publicado en 2020

When do myopia genes have their effect? Comparison of genetic risks between children and adults

artículo científico publicado en 2016

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