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A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder

artículo científico publicado en 2016

Epigenetic prediction of major depressive disorder

artículo científico publicado en 2020

Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis

artículo científico publicado en 2016

Genetic and environmental contributions to psychological resilience and coping

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

artículo científico publicado en 2018

Genetic and environmental risk for chronic pain and the contribution of risk variants for psychiatric disorders. Results from Generation Scotland: Scottish Family Health Study and UK Biobank

article

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 association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP

article

Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

artículo científico publicado en 2021

Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank

artículo científico publicado en 2017

Identification of novel differentially methylated sites with potential as clinical predictors of impaired respiratory function and COPD

artículo científico publicado en 2019

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

artículo científico publicado en 2020

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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

The Stratification Of Major Depressive Disorder Into Genetic Subgroups

scholarly article published 5 May 2017

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