Jennifer L Moran

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Jennifer L



Publications in SciGraph latest 50 shown

  • 2019-01 Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder in NATURE GENETICS
  • 2017-10 Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia in MOLECULAR PSYCHIATRY
  • 2017-10 Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia in MOLECULAR PSYCHIATRY
  • 2017-08 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder 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
  • 2017-03-21 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
  • 2016-09 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder in MOLECULAR PSYCHIATRY
  • 2016-08 Common alleles contribute to schizophrenia in CNV carriers in MOLECULAR PSYCHIATRY
  • 2016-08 Common alleles contribute to schizophrenia in CNV carriers in MOLECULAR PSYCHIATRY
  • 2016-01 Copy number variation in bipolar disorder in MOLECULAR PSYCHIATRY
  • 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
  • 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
  • 2014-01 Evidence that duplications of 22q11.2 protect against schizophrenia in MOLECULAR PSYCHIATRY
  • 2013-12 Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case–control sample in MOLECULAR PSYCHIATRY
  • 2013-11 Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample in MOLECULAR PSYCHIATRY
  • 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
  • 2013-05 Association at SYNE1 in both bipolar disorder and recurrent major depression 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
  • 2012-06 Exome sequencing and the genetic basis of complex traits in NATURE GENETICS
  • 2012-06 ENU mutagenesis in mice identifies candidate genes for hypogonadism in MAMMALIAN GENOME
  • 2012-06 Extremely low-coverage sequencing and imputation increases power for genome-wide association studies in NATURE GENETICS
  • 2012-02 De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia in MOLECULAR PSYCHIATRY
  • 2011-12 A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype in NEURAL DEVELOPMENT
  • 2011-10 Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 in NATURE GENETICS
  • 2011-09 A family-based study of common polygenic variation and risk of schizophrenia in MOLECULAR PSYCHIATRY
  • 2011-05 Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-12 High resolution mapping and positional cloning of ENU-induced mutations in the Rw region of mouse chromosome 5 in BMC GENETICS
  • 2009-07 Agouti C57BL/6N embryonic stem cells for mouse genetic resources in NATURE METHODS
  • 2009-07-01 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder in NATURE
  • 2009-05 An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15 in MAMMALIAN GENOME
  • 2008-04 Genome-wide SNP analysis of Tg.AC transgenic mice reveals an oncogenic collaboration between v-Ha-ras and Ink4a, which is absent in p53 deficiency in ONCOGENE
  • 2007-08 A Mouse Mutation in the 12R-Lipoxygenase, Alox12b, Disrupts Formation of the Epidermal Permeability Barrier in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2006-09 Description and genetic mapping of Polypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations in MAMMALIAN GENOME
  • 1999-06 Limbs move beyond the Radical fringe in NATURE
  • 1999-06 Genomic structure, mapping, and expression analysis of the mammalian Lunatic, Manic, and Radical fringe genes in MAMMALIAN GENOME
  • 1997-02 The Mouse Spam1 maps to proximal Chromosome 6 and is a candidate for the sperm dysfunction in Rb(6.16)24Lub and Rb(6.15)lAld heterozygotes in MAMMALIAN GENOME
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