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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2011-4-8
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pubmed:abstractText |
Rare copy number variants have been implicated in different neurodevelopmental disorders, with the same copy number variants often increasing risk of more than one of these phenotypes. In a discovery sample of 22 schizophrenia patients with an early onset of illness (10-15 years of age), the authors observed in one patient a maternally derived 15q11-q13 duplication overlapping the Prader-Willi/Angelman syndrome critical region. This prompted investigation of the role of 15q11-q13 duplications in psychotic illness.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1535-7228
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pubmed:author |
pubmed-author:AndreassenOle AOA,
pubmed-author:BonettoChiaraC,
pubmed-author:CichonSvenS,
pubmed-author:CollierDavid ADA,
pubmed-author:CraddockNickN,
pubmed-author:DempsterEmmaE,
pubmed-author:DjurovicSrdjanS,
pubmed-author:FrankeBarbaraB,
pubmed-author:GROUP Investigators,
pubmed-author:GieglingInaI,
pubmed-author:GlenthøjBirte YBY,
pubmed-author:GurlingHughH,
pubmed-author:GustafssonOmarO,
pubmed-author:HansenThomasT,
pubmed-author:HreidarssonStefán JSJ,
pubmed-author:IngasonAndrésA,
pubmed-author:IslesAnthony RAR,
pubmed-author:JakobsenKlaus DKD,
pubmed-author:KiemeneyLambertus ALA,
pubmed-author:KirovGeorgeG,
pubmed-author:KristinssonKari TKT,
pubmed-author:MöllerHans-JürgenHJ,
pubmed-author:McQuillinAndrewA,
pubmed-author:MugliaPierandreaP,
pubmed-author:NöthenMarkus MMM,
pubmed-author:O'DonovanMichael CMC,
pubmed-author:OphoffRoel ARA,
pubmed-author:OwenMichael JMJ,
pubmed-author:PeltonenLeenaL,
pubmed-author:PeturssonHannesH,
pubmed-author:PietiläinenOlli P HOP,
pubmed-author:RasmussenHenrik BHB,
pubmed-author:RietschelMarcellaM,
pubmed-author:RujescuDanD,
pubmed-author:SaemundsenEvaldE,
pubmed-author:SigurdssonEngilbertE,
pubmed-author:St ClairDavidD,
pubmed-author:StefanssonHreinnH,
pubmed-author:StefanssonKariK,
pubmed-author:TosatoSarahS,
pubmed-author:WergeThomasT,
pubmed-author:le RouxLouiseL
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pubmed:issnType |
Electronic
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pubmed:volume |
168
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
408-17
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pubmed:meshHeading |
pubmed-meshheading:21324950-Adolescent,
pubmed-meshheading:21324950-Adult,
pubmed-meshheading:21324950-Age of Onset,
pubmed-meshheading:21324950-Blotting, Southern,
pubmed-meshheading:21324950-Child,
pubmed-meshheading:21324950-Chromosomes, Human, Pair 15,
pubmed-meshheading:21324950-DNA Copy Number Variations,
pubmed-meshheading:21324950-Denmark,
pubmed-meshheading:21324950-Female,
pubmed-meshheading:21324950-Genetic Association Studies,
pubmed-meshheading:21324950-Genotype,
pubmed-meshheading:21324950-Great Britain,
pubmed-meshheading:21324950-Humans,
pubmed-meshheading:21324950-Male,
pubmed-meshheading:21324950-Mothers,
pubmed-meshheading:21324950-Prader-Willi Syndrome,
pubmed-meshheading:21324950-Psychotic Disorders,
pubmed-meshheading:21324950-Schizophrenia,
pubmed-meshheading:21324950-Uniparental Disomy,
pubmed-meshheading:21324950-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.
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pubmed:affiliation |
Research Institute of Biological Psychiatry, Mental Health Center Sct. Hans, Copenhagen University Hospital, Roskilde, Denmark.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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