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- W3048018188 endingPage "R50" @default.
- W3048018188 startingPage "R42" @default.
- W3048018188 abstract "Abstract Disruption of chromatin structure due to epimutations is a leading genetic etiology of neurodevelopmental disorders, collectively known as chromatinopathies. We show that there is an increasing level of convergence from the high diversity of genes that are affected by mutations to the molecular networks and pathways involving the respective proteins, the disrupted cellular and subcellular processes, and their consequence for higher order cellular network function. This convergence is ultimately reflected by specific phenotypic features shared across the various chromatinopathies. Based on these observations, we propose that the commonly disrupted molecular and cellular anomalies might provide a rational target for the development of symptomatic interventions for defined groups of genetically distinct neurodevelopmental disorders." @default.
- W3048018188 created "2020-08-13" @default.
- W3048018188 creator A5004763200 @default.
- W3048018188 creator A5013649683 @default.
- W3048018188 date "2020-08-07" @default.
- W3048018188 modified "2023-10-01" @default.
- W3048018188 title "The phenomenal epigenome in neurodevelopmental disorders" @default.
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- W3048018188 doi "https://doi.org/10.1093/hmg/ddaa175" @default.
- W3048018188 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7530535" @default.
- W3048018188 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32766754" @default.
- W3048018188 hasPublicationYear "2020" @default.
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