Bernie Devlin

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Publications in SciGraph latest 50 shown

  • 2018-07 An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders in NATURE GENETICS
  • 2018-05-08 Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls in MOLECULAR PSYCHIATRY
  • 2018-05 An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder in NATURE GENETICS
  • 2018-04 Genetic risk for schizophrenia and psychosis in Alzheimer disease in MOLECULAR PSYCHIATRY
  • 2017-07 Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders in NATURE GENETICS
  • 2017-04 Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples in NATURE GENETICS
  • 2016-11 Gene expression elucidates functional impact of polygenic risk for schizophrenia in NATURE NEUROSCIENCE
  • 2015-12 The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment in NATURE COMMUNICATIONS
  • 2015-12 Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy in NATURE COMMUNICATIONS
  • 2015-02 Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways in NATURE NEUROSCIENCE
  • 2014-12 The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism in NATURE COMMUNICATIONS
  • 2014-12 DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics in MOLECULAR AUTISM
  • 2014-11 Synaptic, transcriptional and chromatin genes disrupted in autism in NATURE
  • 2014-09 A framework for the interpretation of de novo mutation in human disease in NATURE GENETICS
  • 2014-08 Most genetic risk for autism resides with common variation in NATURE GENETICS
  • 2014-08 Response to ‘Predicting the diagnosis of autism spectrum disorder using gene pathway analysis’ in MOLECULAR PSYCHIATRY
  • 2013-12 The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer’s disease in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2012-12 Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis in NATURE GENETICS
  • 2012-12 Common genetic variants, acting additively, are a major source of risk for autism in MOLECULAR AUTISM
  • 2012-12 Genome-wide association study of Alzheimer's disease with psychotic symptoms in MOLECULAR PSYCHIATRY
  • 2012-04-04 De novo mutations revealed by whole-exome sequencing are strongly associated with autism in NATURE
  • 2012-04-04 Patterns and rates of exonic de novo mutations in autism spectrum disorders in NATURE
  • 2012-04 Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis in GENES & IMMUNITY
  • 2011-07 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy in NATURE GENETICS
  • 2010-12 Genetics in psychiatry: common variant association studies in MOLECULAR AUTISM
  • 2010-10 Shedding new light on genetic dark matter in GENOME MEDICINE
  • 2010-07 Functional impact of global rare copy number variation in autism spectrum disorders in NATURE
  • 2009-05 Autism genome-wide copy number variation reveals ubiquitin and neuronal genes in NATURE
  • 2007-07 Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation in HUMAN GENETICS
  • 2007-03 Mapping autism risk loci using genetic linkage and chromosomal rearrangements in NATURE GENETICS
  • 2005-12 Autism and the serotonin transporter: the long and short of it in MOLECULAR PSYCHIATRY
  • 2005-11 Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease in MOLECULAR PSYCHIATRY
  • 2005-09 Association of Multiple DRD2 Polymorphisms with Anorexia Nervosa in NEUROPSYCHOPHARMACOLOGY
  • 2005-09 Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample in MOLECULAR PSYCHIATRY
  • 2005-08 Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia in HUMAN GENETICS
  • 2004-11 Genomic Control to the extreme in NATURE GENETICS
  • 2003-12 Statistical Genetics: False discovery or missed discovery? in HEREDITY
  • 2003-12 Integration of association statistics over genomic regions using Bayesian adaptive regression splines in HUMAN GENOMICS
  • 2003-04 Psychotic symptoms in Alzheimer disease: evidence for a distinct phenotype in MOLECULAR PSYCHIATRY
  • 2002-08 Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau in MOLECULAR PSYCHIATRY
  • 2001-06 Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania in HUMAN GENETICS
  • 2001-02 A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-04 Repositioning the hereditary paraganglioma critical region on chromosome band 11q23 in HUMAN GENETICS
  • 1997-07 The heritability of IQ in NATURE
  • 1988-09 Fractional paternity assignment: theoretical development and comparison to other methods in THEORETICAL AND APPLIED GENETICS
  • 1988-03 Biochemical and morphological evidence for host race evolution in desert mistletoe,Phoradendron californicum (Viscaceae) in PLANT SYSTEMATICS AND EVOLUTION
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