A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
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Recent advances in the genetics of schizophreniaLRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaGenome scan meta-analysis of schizophrenia and bipolar disorder, part II: SchizophreniaDisease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorderDirect measure of the de novo mutation rate in autism and schizophrenia cohortsEnhanced polyubiquitination of Shank3 and NMDA receptor in a mouse model of autismDe novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorderThe glial growth factors deficiency and synaptic destabilization hypothesis of schizophreniaSystematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia.Genetic Consideration of Schizotypal Traits: A ReviewAn association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophreniaA frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorderSchizophrenia genes, gene expression, and neuropathology: on the matter of their convergenceRasd2 Modulates Prefronto-Striatal Phenotypes in Humans and 'Schizophrenia-Like Behaviors' in Mice.Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family Study.Deletion of PLCB1 gene in schizophrenia-affected patients.In vitro binding assays using (3)H nisoxetine and (3)H WIN 35,428 reveal selective effects of gonadectomy and hormone replacement in adult male rats on norepinephrine but not dopamine transporter sites in the cerebral cortex.A novel analytical framework for dissecting the genetic architecture of behavioral symptoms in neuropsychiatric disorders.Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS).Data-driven methodology illustrating mechanisms underlying word list recall: applications to clinical research.An automated method to analyze language use in patients with schizophrenia and their first-degree relativesDTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the geneFinding schizophrenia genes.A population genetic approach to mapping neurological disorder genes using deep resequencing.Genome-wide prediction of imprinted murine genesComparative linkage meta-analysis reveals regionally-distinct, disparate genetic architectures: application to bipolar disorder and schizophrenia.Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.Intraesophageal manganese superoxide dismutase-plasmid liposomes ameliorates novel total-body and thoracic radiation sensitivity of NOS1-/- mice.The genetic relationship between handedness and neurodevelopmental disorders.Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIalpha gene (PIP5K2A) with schizophrenia.Where and what is the right shift factor or cerebral dominance gene? A critique of Francks et al. (2007).Association of the Hermansky-Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects.Genetic Association Analysis of NOS1 and Methamphetamine-Induced Psychosis Among Japanese.Psychotic symptoms in Alzheimer disease: evidence for a distinct phenotype.Schizophrenia, cancer and obstetric complications in an evolutionary perspective-an empirically based hypothesisPossible association between interleukin-1β gene and schizophrenia in a Japanese population.
P2860
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P2860
A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
A genome-wide scan for linkage ...... a or schizoaffective disorder.
@en
A genome-wide scan for linkage ...... a or schizoaffective disorder.
@nl
type
label
A genome-wide scan for linkage ...... a or schizoaffective disorder.
@en
A genome-wide scan for linkage ...... a or schizoaffective disorder.
@nl
prefLabel
A genome-wide scan for linkage ...... a or schizoaffective disorder.
@en
A genome-wide scan for linkage ...... a or schizoaffective disorder.
@nl
P2093
P1476
A genome-wide scan for linkage ...... a or schizoaffective disorder.
@en
P2093
Angela B Smith
Antonio Vita
Betsy Nanthakumar
Gail Shields
John Stewart
Josephine Loftus
Kamran Razi
Lynn E DeLisi
Margherita Comazzi
Nigel Wellman
P304
P356
10.1176/APPI.AJP.159.5.803
P407
P577
2002-05-01T00:00:00Z