About: Phenotypic variations on the theme of CNVs

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Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2008 (uk) im Dezember 2008 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57419525-2D4EFB5E-23C1-403E-A9E2-C8D8C9FEC3A2
publication date	2008-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57419525-55593538-FD96-4571-BAD0-65E6A16A22C9
language of work or name	English
exact match	wds:Q57419525-3234C7D0-F99E-443C-9E5F-071F6B15E868
exact match	https://scigraph.springernature.com/pub.10.1038/ng1208-1392
cites work	wds:Q57419525-02597DE2-BF5A-4749-A22F-8EB0E79DA43F wds:Q57419525-0E1859AB-D100-4ADD-AD97-65F6EB6013F3 wds:Q57419525-1738D7AC-7831-4A69-A115-13A1B19B9B8B wds:Q57419525-1EBFB648-4898-47CF-8775-CF8EB7420242 wds:Q57419525-48C1F201-3142-4D96-A528-84E14EC592D1 wds:Q57419525-6217881F-5B18-46E0-89B6-514B7122E3D6 wds:Q57419525-8E4C55B3-0431-453F-8D2C-FB2E95F9F44A wds:Q57419525-A2B151CF-5B48-477F-8444-E077A1FAF98A wds:Q57419525-BB85F20B-D99E-4712-8ED9-13C4A80278D5 wds:Q57419525-D3605FCA-1DB4-4588-9178-616002F766F7 wds:Q57419525-DE6700E5-6AAF-4853-A2EF-8295963AD38D wds:Q57419525-E7610CF3-6B56-4461-BE14-EB299BCC24FD wds:Q57419525-EB156CF1-33B0-4427-B135-4027CC5439D0
cites work	Integrated detection and population-genetic analysis of SNPs and copy number variation Copy-number variations associated with neuropsychiatric conditions Global variation in copy number in the human genome Large-scale copy number polymorphism in the human genome Rare chromosomal deletions and duplications increase risk of schizophrenia Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities Large recurrent microdeletions associated with schizophrenia Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes Obstetric complications and schizophrenia: historical and meta-analytic review Premorbid IQ in schizophrenia: a meta-analytic review Intermediate phenotypes and genetic mechanisms of psychiatric disorders Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia Endophenotypes in psychiatric genetics.
author name string	wds:Q57419525-3CAE32D3-9F9C-4444-ABDA-D7E391AE1539
author name string	Michael J Owen
rdfs:label	Phenotypic variations on the theme of CNVs (en) Phenotypic variations on the theme of CNVs (nl)
skos:prefLabel	Phenotypic variations on the theme of CNVs (en) Phenotypic variations on the theme of CNVs (nl)
name	Phenotypic variations on the theme of CNVs (en) Phenotypic variations on the theme of CNVs (nl)
author	wds:Q57419525-3844576C-1EF6-4A5C-AFAD-C54A1E1EA92B wds:Q57419525-C55698C6-B13A-42DB-B015-E10C5694045A
author	George Kirov Michael C O'Donovan
title	wds:Q57419525-B011097B-6D37-4C81-91F8-43CD2D81B9C2
title	Phenotypic variations on the theme of CNVs (en)
page(s)	wds:Q57419525-BBC24571-ABC1-49D6-8F51-0634CF77FBB9
page(s)	1392-1393
instance of	wds:Q57419525-FD66C4C6-DCFC-452E-A156-DB74BC311875
instance of	scholarly article
PubMed ID	wds:Q57419525-0682BAFD-69DB-47C3-9E31-A3E23874C8DB
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19029974
PubMed ID	19029974
published in	wds:Q57419525-29A241B1-CC72-4B05-83FE-1F2ADCE2F9A3
published in	Nature Genetics
issue	wds:Q57419525-0CE0E766-9373-4954-BF78-BA7AD688D1F4
volume	wds:Q57419525-01E785EC-5419-42BA-AED6-61A0FE8D1ABD
issue	12
volume	40
DOI	wds:Q57419525-B0DA3B0B-A1D0-4131-88D3-C55ED8C992B4
DOI	http://dx.doi.org/10.1038/NG1208-1392
DOI	10.1038/NG1208-1392
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57419525
is cites work of	Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics? Schizophrenia The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders Copy number variations of chromosome 16p13.1 region associated with schizophrenia A genome-wide investigation of SNPs and CNVs in schizophrenia Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders. The clinical context of copy number variation in the human genome The phenotypic manifestations of rare genic CNVs in autism spectrum disorder Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychoses Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia SnoopCGH: software for visualizing comparative genomic hybridization data High rate of disease-related copy number variations in childhood onset schizophrenia. Neurexin 1 (NRXN1) deletions in schizophrenia Annual research review: impact of advances in genetics in understanding developmental psychopathology. Penetrance for copy number variants associated with schizophrenia. Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders. Integrative genetical genomics in Arabidopsis Autism risk across generations: a population-based study of advancing grandpaternal and paternal age. Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia Increased de novo copy number variants in the offspring of older males Psychopathology and cognition in children with 22q11.2 deletion syndrome Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants Understanding variable expressivity in microdeletion syndromes. Genetic insights into the neurodevelopmental origins of schizophrenia. Reduced burden of very large and rare CNVs in bipolar affective disorder. Psychiatric disorders in children with 16p11.2 deletion and duplication A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk Etiologies and molecular mechanisms of communication disorders Genes and Small RNA Transcripts Exhibit Dosage-Dependent Expression Pattern in Maize Copy-Number Alterations. VCS: Tool for Visualizing Copy Number Variation and Single Nucleotide Polymorphism Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.

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