The phenotypic manifestations of rare CNVs in schizophrenia

[1]  Oar,et al.  Cary, North Carolina , 2015 .

[2]  N. Andreasen.  Scale for the Assessment of Negative Symptoms , 2014 .

[3]  P. Mortensen,et al.  Population impact of familial and environmental risk factors for schizophrenia: A nationwide study , 2014, Schizophrenia Research.

[4]  E. Rees,et al.  Analysis of copy number variations at 15 schizophrenia-associated loci , 2014, The British journal of psychiatry : the journal of mental science.

[5]  K. Quinn,et al.  The NIMH Research Domain Criteria (RDoC) Project: implications for genetics research , 2014, Mammalian Genome.

[6]  Bradley P. Coe,et al.  An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis , 2014, Human molecular genetics.

[7]  P. Visscher,et al.  A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability , 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[8]  G. Kirov,et al.  CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 , 2013, Human molecular genetics.

[9]  C. Hultman,et al.  Autism risk across generations: a population-based study of advancing grandpaternal and paternal age. , 2013, JAMA psychiatry.

[10]  K. Lampi,et al.  Parental Age and Risk of Autism Spectrum Disorders in a Finnish National Birth Cohort , 2013, Journal of Autism and Developmental Disorders.

[11]  P. Donnelly,et al.  Schizophrenia genetic variants are not associated with intelligence , 2013, Psychological Medicine.

[12]  J. Buizer-Voskamp,et al.  Increased paternal age and the influence on burden of genomic copy number variation in the general population , 2013, Human Genetics.

[13]  Lorna M. Lopez,et al.  Genetic Copy Number Variation and General Cognitive Ability , 2012, PloS one.

[14]  Michael John Owen,et al.  Genome-Wide Association Study Implicates HLA-C*01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia , 2012, Biological Psychiatry.

[15]  S. Steinberg,et al.  Rate of de novo mutations and the importance of father’s age to disease risk , 2012, Nature.

[16]  G. Kirov,et al.  De novo mutation in schizophrenia. , 2012, Schizophrenia bulletin.

[17]  J. Doherty,et al.  Recent genomic advances in schizophrenia , 2012, Clinical genetics.

[18]  B. O’Donoghue,et al.  Can we combine symptom scales for collaborative research projects? , 2012, Journal of psychiatric research.

[19]  J. Sebat,et al.  High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia , 2011, Neuron.

[20]  J. Suvisaari,et al.  Advanced paternal age and parental history of schizophrenia , 2011, Schizophrenia Research.

[21]  C. Hultman,et al.  Advanced paternal and grandpaternal age and schizophrenia: A three-generation perspective , 2011, Schizophrenia Research.

[22]  S Purcell,et al.  De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia , 2011, Molecular Psychiatry.

[23]  M. Järvelin,et al.  Meta-analysis of paternal age and schizophrenia risk in male versus female offspring. , 2011, Schizophrenia bulletin.

[24]  J. Sebat,et al.  Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia , 2011, Nature.

[25]  Jianxin Shi,et al.  Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. , 2011, The American journal of psychiatry.

[26]  J. Sebat,et al.  Duplications of the Neuropeptide Receptor VIPR2 Confer Significant Risk for Schizophrenia , 2011, Nature.

[27]  D. Rujescu,et al.  A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809 , 2011, Schizophrenia Research.

[28]  Alan S. Brown.  The environment and susceptibility to schizophrenia , 2011, Progress in Neurobiology.

[29]  Stephan J Sanders,et al.  Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. , 2010, American journal of human genetics.

[30]  A. Minelli,et al.  New Copy Number Variations in Schizophrenia , 2010, PloS one.

[31]  Joshua M. Korn,et al.  Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function , 2010, PLoS genetics.

[32]  D. Cutler,et al.  Microdeletions of 3q29 confer high risk for schizophrenia. , 2010, American journal of human genetics.

[33]  Gary D Bader,et al.  Functional impact of global rare copy number variation in autism spectrum disorders , 2010, Nature.

[34]  R. Heinssen,et al.  Research domain criteria (RDoC): toward a new classification framework for research on mental disorders. , 2010, The American journal of psychiatry.

[35]  Richard Redon,et al.  Confirmed rare copy number variants implicate novel genes in schizophrenia. , 2010, Biochemical Society transactions.

[36]  E. Baca-García,et al.  Differences in maternal and paternal age between Schizophrenia and other psychiatric disorders , 2010, Schizophrenia Research.

[37]  M. Gill,et al.  Replicated genetic evidence supports a role for HOMER2 in schizophrenia , 2010, Neuroscience Letters.

[38]  A. Barnett,et al.  Maternal age and paternal age are associated with distinct childhood behavioural outcomes in a general population birth cohort , 2009, Schizophrenia Research.

[39]  Michael Gill,et al.  Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects. , 2009, Archives of general psychiatry.

[40]  Laurence Faivre,et al.  Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation. , 2009, Archives of general psychiatry.

[41]  G. Kirov,et al.  Phenotypic variations on the theme of CNVs , 2008, Nature Genetics.

[42]  Jennifer Couzin,et al.  Interest Rises in DNA Copy Number Variations--Along With Questions , 2008, Science.

[43]  J. Buizer-Voskamp,et al.  Recurrent CNVs disrupt three candidate genes in schizophrenia patients. , 2008, American journal of human genetics.

[44]  Joshua M. Korn,et al.  Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs , 2008, Nature Genetics.

[45]  Thomas W. Mühleisen,et al.  Large recurrent microdeletions associated with schizophrenia , 2008, Nature.

[46]  P. Visscher,et al.  Rare chromosomal deletions and duplications increase risk of schizophrenia , 2008, Nature.

[47]  Joseph A. Gogos,et al.  Strong association of de novo copy number mutations with sporadic schizophrenia , 2008, Nature Genetics.

[48]  D. Malaspina,et al.  Growth and schizophrenia: aetiology, epidemiology and epigenetics. , 2008, Novartis Foundation symposium.

[49]  W. Honer,et al.  DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling. , 2006, Human molecular genetics.

[50]  C. Frith,et al.  Theory of mind , 2005, Current Biology.

[51]  L. Heffner.  Advanced maternal age--how old is too old? , 2004, The New England journal of medicine.

[52]  G. McVean,et al.  Evidence for Selective Advantage of Pathogenic FGFR2 Mutations in the Male Germ Line , 2003, Science.

[53]  I. Gottesman,et al.  The endophenotype concept in psychiatry: etymology and strategic intentions. , 2003, The American journal of psychiatry.

[54]  S. Baron-Cohen,et al.  The "Reading the Mind in the Eyes" Test revised version: a study with normal adults, and adults with Asperger syndrome or high-functioning autism. , 2001, Journal of child psychology and psychiatry, and allied disciplines.

[55]  R. Bentall,et al.  A new measure of causal locus: the internal, personal and situational attributions questionnaire , 1996 .

[56]  C. Frith,et al.  Schizophrenia, symptomatology and social inference: Investigating “theory of mind” in people with schizophrenia , 1995, Schizophrenia Research.

[57]  I. Gottesman.  Schizophrenia Genesis: The Origins of Madness , 1990 .

[58]  Aiden Corvin,et al.  Genome-Wide Association Study Implicates HLA-C*01: 02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia Irish Schizophrenia Genomics Consortium and the Wellcome Trust Case Control Consortium 2 , 2012 .

[59]  D. St. Clair,et al.  Copy number variation and schizophrenia. , 2009, Schizophrenia bulletin.

[60]  Alex E. Lash,et al.  Gene Expression Omnibus: NCBI gene expression and hybridization array data repository , 2002, Nucleic Acids Res..

[61]  S. Kay,et al.  The positive and negative syndrome scale (PANSS) for schizophrenia. , 1987, Schizophrenia bulletin.