List of works - Bernie Devlin

A framework for the interpretation of de novo mutation in human disease

scientific article (publication date: 3 August 2014)

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

scientific article published on 10 June 2020

Alcohol Use Disorder Comorbidity in Eating Disorders

scholarly article by Cynthia Bulik et al published 15 July 2004 in The Journal of Clinical Psychiatry

Alcohol use disorder comorbidity in eating disorders: a multicenter study

scientific article

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

scientific article

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

scientific article

Common risk variants identified in autism spectrum disorder

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

scientific article

Correction to: Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD

scientific article published on 07 September 2020

De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

scientific article published on 08 October 2020

Evaluation of HLA polymorphisms in relation to schizophrenia risk and infectious exposure

scientific article

Functional impact of global rare copy number variation in autism spectrum disorders

scientific article published on 15 July 2010

Genetic analysis of bulimia nervosa: methods and sample description

scientific article published in May 2004

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

scientific article published on 16 June 2015

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

scientific article

Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD

scientific article published on 09 July 2020

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

scientific article

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates

scientific article published on November 2005

Linkage analysis of anorexia nervosa incorporating behavioral covariates

scientific article published in March 2002

Most genetic risk for autism resides with common variation ⬇️

scientific article

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Patterns and rates of exonic de novo mutations in autism spectrum disorders

scientific article

Personality characteristics of women before and after recovery from an eating disorder

scientific article published in November 2004

Personality in men with eating disorders

scientific article published in September 2004

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects ⬇️

scientific article published on January 10, 2012

Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients

scientific article

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

scientific article published on January 2013

Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk

scientific article published in 2022

Selection of eating-disorder phenotypes for linkage analysis

scientific article published on November 2005

Testing for an unusual distribution of rare variants

scientific article

The genetics of anorexia nervosa collaborative study: methods and sample description

scientific article published on May 2008

List of works by Bernie Devlin

A framework for the interpretation of de novo mutation in human disease

A genome-wide scan for common alleles affecting risk for autism

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

Alcohol Use Disorder Comorbidity in Eating Disorders

Alcohol use disorder comorbidity in eating disorders: a multicenter study

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Common risk variants identified in autism spectrum disorder

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

Correction to: Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD

De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

Evaluation of HLA polymorphisms in relation to schizophrenia risk and infectious exposure

Functional impact of global rare copy number variation in autism spectrum disorders

Genetic analysis of bulimia nervosa: methods and sample description

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

Individual common variants exert weak effects on the risk for autism spectrum disorders

Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates

Linkage analysis of anorexia nervosa incorporating behavioral covariates

Most genetic risk for autism resides with common variation ⬇️

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Personality characteristics of women before and after recovery from an eating disorder

Personality in men with eating disorders

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects ⬇️

Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk

Selection of eating-disorder phenotypes for linkage analysis

Testing for an unusual distribution of rare variants

The genetics of anorexia nervosa collaborative study: methods and sample description