Douglas M Ruderfer

Ontology type: schema:Person     

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Douglas M



Publications in SciGraph latest 50 shown

  • 2019-01-04 Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide in MOLECULAR PSYCHIATRY
  • 2018-12 Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records in TRANSLATIONAL PSYCHIATRY
  • 2018-12 Unperturbed expression bias of imprinted genes in schizophrenia in NATURE COMMUNICATIONS
  • 2018-12 Improving genetic prediction by leveraging genetic correlations among human diseases and traits in NATURE COMMUNICATIONS
  • 2018-03 Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection in NATURE GENETICS
  • 2017-12 Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders in GENOME MEDICINE
  • 2017-12 Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains in NATURE COMMUNICATIONS
  • 2017-12 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function in SCIENTIFIC REPORTS
  • 2017-08 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder in MOLECULAR PSYCHIATRY
  • 2017-03-21 Genetic correlation between amyotrophic lateral sclerosis and schizophrenia in NATURE COMMUNICATIONS
  • 2017-01 Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder in TRANSLATIONAL PSYCHIATRY
  • 2017-01 Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects in NATURE GENETICS
  • 2016-11 Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia in NATURE NEUROSCIENCE
  • 2016-11 Gene expression elucidates functional impact of polygenic risk for schizophrenia in NATURE NEUROSCIENCE
  • 2016-10 Patterns of genic intolerance of rare copy number variation in 59,898 human exomes in NATURE GENETICS
  • 2016-09 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder in MOLECULAR PSYCHIATRY
  • 2016-08 Deep phenotyping predicts Huntington's genotype in NATURE BIOTECHNOLOGY
  • 2016-08 Analysis of protein-coding genetic variation in 60,706 humans in NATURE
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-07 Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia in TRANSLATIONAL PSYCHIATRY
  • 2015-04 No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-02 Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways in NATURE NEUROSCIENCE
  • 2014-09 Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia in MOLECULAR PSYCHIATRY
  • 2014-07 Copy number variation in schizophrenia in Sweden in MOLECULAR PSYCHIATRY
  • 2014-07 Biological insights from 108 schizophrenia-associated genetic loci in NATURE
  • 2014-02 A polygenic burden of rare disruptive mutations in schizophrenia in NATURE
  • 2014-02 De novo mutations in schizophrenia implicate synaptic networks in NATURE
  • 2013-10 Genome-wide association analysis identifies 13 new risk loci for schizophrenia in NATURE GENETICS
  • 2013-09 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs in NATURE GENETICS
  • 2013-09 Mosaic copy number variation in schizophrenia in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-08 Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder in MOLECULAR PSYCHIATRY
  • 2012-09 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder in MOLECULAR PSYCHIATRY
  • 2012-02 De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia in MOLECULAR PSYCHIATRY
  • 2011-10 Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 in NATURE GENETICS
  • 2011-10 Genome-wide association study identifies five new schizophrenia loci in NATURE GENETICS
  • 2011-09 A family-based study of common polygenic variation and risk of schizophrenia in MOLECULAR PSYCHIATRY
  • 2010-01 Family-based genetic risk prediction of multifactorial disease in GENOME MEDICINE
  • 2009-03 Comprehensive polymorphism survey elucidates population structure of Saccharomyces cerevisiae in NATURE
  • 2008-09 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder in NATURE GENETICS
  • 2007-11 Genetic basis of proteome variation in yeast in NATURE GENETICS
  • 2007-04 Genetic basis of individual differences in the response to small-molecule drugs in yeast in NATURE GENETICS
  • 2006-09 Population genomic analysis of outcrossing and recombination in yeast in NATURE GENETICS
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