Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.
about
Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigreesGenome scan meta-analysis of schizophrenia and bipolar disorder, part II: SchizophreniaGenomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.Association of neuregulin 1 with schizophrenia confirmed in a Scottish populationGenetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophreniaInteraction between interleukin 3 and dystrobrevin-binding protein 1 in schizophreniaEvidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunitCognitive heterogeneity in schizophrenia.Association study of polymorphisms in the neutral amino acid transporter genes SLC1A4, SLC1A5 and the glycine transporter genes SLC6A5, SLC6A9 with schizophrenia.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).A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestryAssociation study of SNAP25 and schizophrenia in Irish family and case-control samples.FBXL21 association with schizophrenia in Irish family and case-control samples.DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the geneLinkage analysis of schizophrenia controlling for population substructure.Analysis of protocadherin alpha gene enhancer polymorphism in bipolar disorder and schizophrenia.Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate.Comparative linkage meta-analysis reveals regionally-distinct, disparate genetic architectures: application to bipolar disorder and schizophrenia.Influence of the NR3A subunit on NMDA receptor functions.Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1Identification of novel schizophrenia loci by homozygosity mapping using DNA microarray analysisAssociation study of DTNBP1 with schizophrenia in a US sample.Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit.Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness.Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.Reduced dysbindin expression mediates N-methyl-D-aspartate receptor hypofunction and impaired working memory performance.Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophreniaContribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients.Genetic association of single nucleotide polymorphisms in dystrobrevin binding protein 1 gene with schizophrenia in a Malaysian population.Genome scans and gene expression microarrays converge to identify gene regulatory loci relevant in schizophreniaConvergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.Meta-analysis of 32 genome-wide linkage studies of schizophrenia.Is the histidine triad nucleotide-binding protein 1 (HINT1) gene a candidate for schizophrenia?Abnormal expression of myelination genes and alterations in white matter fractional anisotropy following prenatal viral influenza infection at E16 in mice.Regulation of neural circuit formation by protocadherins.Analysis of opo cis-regulatory landscape uncovers Vsx2 requirement in early eye morphogenesis.Shared and specific susceptibility loci for schizophrenia and bipolar disorder: a dense genome scan in Eastern Quebec families.Identification of blood biomarkers for psychosis using convergent functional genomics.
P2860
Q21198693-949E4853-373B-45F1-A954-8B8A500FC481Q24532517-6C483AE8-7742-4AF3-AEAE-C649709AED1BQ24540539-34956B49-A30A-437B-B91B-B4F07A924837Q24561773-AE2131EE-C518-4FD3-9F5C-FE0CECE0EDE9Q24612644-305F7B7C-1A87-4F85-ADC4-93A1B016B9C1Q24651143-1C221FCD-1BE8-4A3A-8A9A-5223CA9AF6B3Q24678549-3215D21F-24C3-430A-8829-555754DF37F1Q31108406-B300C3F5-0001-44E6-96CD-0E386EE82EE8Q33353046-2CF7B7D2-520D-48ED-9814-E74CEAC9C2BCQ33570929-093B3681-A57C-4FC2-B238-DD9E0CEE40A7Q33798551-20573374-27EC-41E4-8744-CD21D9DA4AC2Q33809007-ACCDF97B-638C-4FE1-BA85-D7B681641679Q33809021-B5D766E2-4A12-43BA-8E56-1997CA7FCF9EQ33818087-188EF76C-4200-46CC-BC1D-9D0BCEF40408Q33819408-10A8BDD1-25A9-4FBA-8263-5D099826FCF0Q33821683-D3461FCA-2309-45B4-922E-81A7F12CA58EQ33846861-50A9CF2F-86B7-47DA-AF91-02F271B1F353Q33895253-ECD72E9E-1573-4681-A1D6-CD7D275464F6Q33906149-42E2754F-6743-4E7B-8931-2DC2ECE2F6EBQ33910975-FA0432B9-167D-4135-A04D-139A48EDF422Q33927060-97B3A04B-05BA-464F-A938-C12DEF9A5A02Q34019925-F72608C6-6B2A-4637-B4EB-45D76AE021ABQ34021154-FC52EAF0-5DA4-475A-BCAD-BBD0C0947028Q34119018-FFE93DEA-B048-41A8-8853-21713B0BC4A0Q34137538-6193AC09-4AB1-4134-95C3-AC79853CF0C5Q34379851-2B49EBCE-B324-4D54-8BA1-D63C49BA5EC1Q34452249-BD6347C4-3E15-450E-8FFF-CECB1513DAD8Q34856932-77980291-D6F0-4B7F-A220-7E32B63090A4Q35221473-11888555-BD2D-4B26-A5C8-5365C017E978Q35544796-7076B984-ECB5-4D6C-9EA0-1BA4F92BE711Q35933583-E32E3F3E-E7BB-4A29-88D4-BBA12AE04BB4Q36140929-8C757954-E921-4898-BC4A-60C9311BB666Q36189837-2C46F639-0003-42AD-8922-3273944CF1D7Q37274086-A2E5596B-F647-47F7-9D72-CF88FA1E37E6Q37312173-B1D2C311-4521-46B7-8C6A-07260E23BF35Q37327075-82155F3D-73C0-41C8-85C4-52FBFA2ADD04Q38718127-57563DE6-01E3-442B-B0D5-353000CB3D31Q40951115-F61D20B0-0FFB-4C7E-A3B9-6AEB43E69084Q42640185-D73FAC08-96BD-48A1-B7D4-B5DBB94405D6Q43616392-B26EDAD5-4FEE-4CA8-B2A0-20936357E874
P2860
Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh
2002年學術文章
@zh-hant
name
Genome-wide scans of three ind ...... multiple susceptibility genes.
@en
Genome-wide scans of three ind ...... multiple susceptibility genes.
@nl
type
label
Genome-wide scans of three ind ...... multiple susceptibility genes.
@en
Genome-wide scans of three ind ...... multiple susceptibility genes.
@nl
prefLabel
Genome-wide scans of three ind ...... multiple susceptibility genes.
@en
Genome-wide scans of three ind ...... multiple susceptibility genes.
@nl
P2093
P2860
P356
P1433
P1476
Genome-wide scans of three ind ...... multiple susceptibility genes.
@en
P2093
Harris-Kerr C
MacLean CJ
Myakishev MV
O'Neill FA
P2860
P2888
P304
P356
10.1038/SJ.MP.4001051
P407
P577
2002-01-01T00:00:00Z
P5875
P6179
1012301787