RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing - Wikidata - awgldk - TriplyDB

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

http://www.wikidata.org/entity/Q34863571

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Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population.

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RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

http://www.wikidata.org/entity/Q34863571

description

2011 nî lūn-bûn

@nan

2011 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

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2011年论文

@wuu

name

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@ast

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@en

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

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type

label

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@ast

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@en

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@nl

prefLabel

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@ast

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@en

RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@nl

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P356

J.BIOPSYCH.2010.10.022

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Biological Psychiatry

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RELN rs7341475 and schizophrenia risk: confusing, yet somehow intriguing

@en

P2860

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans

Reelin promoter hypermethylation in schizophrenia

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

Genotype, haplotype and copy-number variation in worldwide human populations

A genome-wide investigation of SNPs and CNVs in schizophrenia.

No effect of a common allelic variant in the reelin gene on intermediate phenotype measures of brain structure, brain function, and gene expression

Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women.

Methylation status of the reelin promoter region in the brain of schizophrenic patients.

Reelin glycoprotein: structure, biology and roles in health and disease.

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e19

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scholarly article

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10.1016/J.BIOPSYCH.2010.10.022

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5

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Daniel R. Weinberger

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2011-03-01T00:00:00Z

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51089115

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21532921

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