Effects of cis-regulatory variation differ across regions of the adult human brain (scientific article published on 9 September 2010)

Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction

Q28298082

Identification of loci associated with schizophrenia by genome-wide association and follow-up

Q29417130

Genetics of gene expression and its effect on disease

Q29614591

Common regulatory variation impacts gene expression in a cell type-dependent manner

Q29614882

Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample

Q33554950

Allelic skewing of DNA methylation is widespread across the genome

Q33645884

Allelic variation in gene expression is common in the human genome

Q33682674

Allelic imbalance (AI) identifies novel tissue-specific cis-regulatory variation for human UGT2B15

Q34067581

Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human

Q37343820

Genomic imprinting: employing and avoiding epigenetic processes

Q37362832

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

Q37571848

Widespread monoallelic expression on human autosomes

Q40050793

Context-specific functional effects of IFNGR1 promoter polymorphism

Q40294843

Allele-specific DNA methylation in mouse strains is mainly determined by cis-acting sequences

Q41827630

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

Q42676740

Convergent evidence for impaired AKT1-GSK3beta signaling in schizophrenia

Q44743796

Influence of functional variant of neuronal nitric oxide synthase on impulsive behaviors in humans

Q46174409

Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4.

Q48179338

Cis-acting variation in the expression of a high proportion of genes in human brain

Q48319040

Detection of regulatory variation in mouse genes

Q48456623

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.

Q53621277

Allelic Variation in Human Gene Expression

Q57293497

Low mRNA levels of RGS4 splice variants in Alzheimer's disease: association between a rare haplotype and decreased mRNA expression

Q81633585

P433

issue

P407

language of work or name

English

Q1860

P304

page(s)

4490-4496

P577

publication date

2010-09-09

P1433

published in

Human Molecular Genetics

Q2720965

P1476

title

Effects of cis-regulatory variation differ across regions of the adult human brain

P478

volume

Reverse relations

cites work (P2860)

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