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Author Details

Bernie Devlin
1985
220
80
PMIDPaper TitleJournal TitlePublished Year
37100590Direct additive genetics and maternal effect contribute to the risk of Tourette disorder.J Neurol Neurosurg Psychiatry2023
36123423Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review.Mol Psychiatry2023
37595579Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.Am J Hum Genet2023
37986747Comparison of gene expression in living and postmortem human brain.medRxiv2023
37790341Evaluating and Improving Health Equity and Fairness of Polygenic Scores.2023
37773317Heritable Composite Phenotypes Defined by Combinations of Conduct Problem, Depression, and Temperament Features: Contributions to risk for Alcohol Problems.2023
37128669Adapting Patient and Public Involvement processes in response to the Covid-19 pandemic.2023
34789012The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.Am J Psychiatry2022
35987687Schizophrenia-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.Transl Psychiatry2022
36323256Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development.Cell Rep2022
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
34154796Sex Differences in the Human Brain Transcriptome of Cases With Schizophrenia.Biol Psychiatry2022
34615521How rare and common risk variation jointly affect liability for autism spectrum disorder.Mol Autism2021
34112972Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease.Mol Psychiatry2021
33837133Bayesian estimation of cell type-specific gene expression with prior derived from single-cell data.Genome Research2021
33723209Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder.Transl Psychiatry2021
33714545Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum.Biol Psychiatry2021
33372276H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives.Annals of Human Genetics2021
34459489An approach to gene-based testing accounting for dependence of tests among nearby genes.Briefings in Bioinformatics2021
34615535Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.Mol Autism2021
31424081Resting-State Functional Network Organization Is Stable Across Adolescent Development for Typical and Psychosis Spectrum Youth.Schizophrenia Bulletin2020
32268104Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.Cell Rep2020
32199606Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder.Biol Psychiatry2020
31907560Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS).Soc Psychiatry Psychiatr Epidemiol2020
31928911Age dependent association of inbreeding with risk for schizophrenia in Egypt.Schizophrenia Research2020
32652852Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5-years apart.Human Brain Mapping2020
32648044Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD.Journal of Abnormal Child Psychology2020
33032641De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types.Mol Autism2020
32522875A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk.Proceedings of the National Academy of Sciences of the United States of America2020
32894416Correction to: Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD.Journal of Abnormal Child Psychology2020
33157004Not All Autism Genes Are Created Equal: A Response to Myers et al.Am J Hum Genet2020
30862939Correction: Genetic risk for schizophrenia and psychosis in Alzheimer disease.Mol Psychiatry2020
31400192Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression.2020
31086353Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.Nat Genet2019
31551426CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder.Sci Data2019
30587579Semisoft clustering of single-cell data.Proceedings of the National Academy of Sciences of the United States of America2019
29740122Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls.Mol Psychiatry2019
30983407Variations in Genes Related to Sleep Patterns in Children With Autism Spectrum Disorder.Biol Res Nurs2019
29805045Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS.Am J Hum Genet2018
28461698Genetic risk for schizophrenia and psychosis in Alzheimer disease.Mol Psychiatry2018
30174778A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA.Annals of Applied Statistics2018
29892012An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders.Nat Genet2018
30545852Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.Science2018
29100626Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden.Biol Psychiatry2018
29306175Joint evaluation of serum C-Reactive Protein levels and polygenic risk scores as risk factors for schizophrenia.Psychiatry Research2018
29700473An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.Nat Genet2018
28191890Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.Nat Genet2017
28504703Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.Nat Genet2017
28426285The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability.Annual Review of Genomics and Human Genetics2017
28570395Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred.Psychiatr Genet2017
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