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• W2886367104 abstract "Abstract Schizophrenia genome-wide association studies have identified >150 regions of the genome associated with disease risk, yet there is little evidence that coding mutations contribute to this disorder. To explore the mechanism of non-coding regulatory elements in schizophrenia, we performed ATAC-seq on adult prefrontal cortex brain samples from 135 individuals with schizophrenia and 137 controls, and identified 118,152 ATAC-seq peaks. These accessible chromatin regions in the brain are highly enriched for schizophrenia SNP heritability. Accessible chromatin regions that overlap evolutionarily conserved regions exhibit an even higher heritability enrichment, indicating that sequence conservation can further refine functional risk variants. We identify few differences in chromatin accessibility between cases and controls, in contrast to thousands of age-related differential accessible chromatin regions. Altogether, we characterize chromatin accessibility in the human prefrontal cortex, the effect of schizophrenia and age on chromatin accessibility, and provide evidence that our dataset will allow for fine mapping of risk variants." @default.
• W2886367104 created "2018-08-22" @default.
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• W2886367104 date "2018-08-07" @default.
• W2886367104 modified "2023-10-17" @default.
• W2886367104 title "Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia" @default.
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• W2886367104 doi "https://doi.org/10.1038/s41467-018-05379-y" @default.
• W2886367104 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6081462" @default.
• W2886367104 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30087329" @default.
• W2886367104 hasPublicationYear "2018" @default.

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