Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 - Wikidata - wikimedia - TriplyDB

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

http://www.wikidata.org/entity/Q28281769

about

Association study of the vesicular monoamine transporter 1 (VMAT1) gene with schizophrenia in a Japanese population Recent advances in the genetics of schizophrenia Genomewide scans of complex human diseases: true linkage is hard to find Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23 Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios Genomewide 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.Genetic variation in the 22q11 locus and susceptibility to schizophrenia Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease Association of neuregulin 1 with schizophrenia confirmed in a Scottish population Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia Neuregulin 1 and susceptibility to schizophrenia.Methamphetamine-associated psychosis.Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar i disorder Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia G72/G30 genes and schizophrenia: a systematic meta-analysis of association studies Disruption of the neuronal PAS3 gene in a family affected with schizophrenia Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit Genome scans and microarrays: converging on genes for schizophrenia?Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5)The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia.Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22 Genome-wide scan for loci of Asperger syndrome An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia The NPAS3 gene--emerging evidence for a role in psychiatric illness Interacting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorder A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42 The ups and downs of Wnt signaling in prevalent neurological disorders A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms Psychiatric genetics: back to the future Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence Behavioral, Neurophysiological, and Synaptic Impairment in a Transgenic Neuregulin1 (NRG1-IV) Murine Schizophrenia Model.From genomics to proteomics: new directions in molecular neuropsychiatry.Deletion of PLCB1 gene in schizophrenia-affected patients.Evidence of missense mutations on the neuregulin 1 gene affecting function of prepulse inhibition Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes.

P2860

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P2860

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

http://www.wikidata.org/entity/Q28281769

description

1998 nî lūn-bûn

@nan

1998 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

name

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@ast

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@en

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@nl

type

label

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@ast

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@en

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@nl

prefLabel

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@ast

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@en

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

@nl

P1433

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P1433

Nature Genetics

P1476

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

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P2093

A Chakravarti

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A E Pulver

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B A Dombroski

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B Childs

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C Gehrig

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C N Stefanis

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D E Housman

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D G Dikeos

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G N Papadimitriou

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G Nestadt

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P2860

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus.

Path analysis of qualitative data on pairs of relatives: application to schizophrenia.

The case for heterogeneity in the etiology of schizophrenia.

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome.

Risk factors in schizophrenia. Season of birth, gender, and familial risk.

Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families.

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

P2888

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70-3

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10.1038/1734

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P433

1

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20

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Stylianos Antonarakis

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13553307

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P921

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