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Genomic views of distant-acting enhancers
Open accessAbstract
In contrast to protein-coding sequences, the significance of variation in non-coding DNA in human disease has been minimally explored. A great number of recent genome-wide association studies suggest that non-coding variation is a significant risk factor for common disorders, but the mechanisms by which this variation contributes to disease remain largely obscure. Distant-acting transcriptional enhancers--a major category of functional non-coding DNA--are involved in many developmental and disease-relevant processes. Genome-wide approaches to their discovery and functional characterization are now available and provide a growing knowledge base for the systematic exploration of their role in human biology and disease susceptibility.
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“most genetic variation that contributes to common psychiatric disorders is not in protein-coding regions”
From Defining the genetic, genomic, cellular, and diagnostic architectures of psychiatric disorders (2019) · cites this paper as Visel et al., 2009
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“The majority of disease-associated genetic variation lies in non-coding regions (7) enriched for non-coding RNAs and cis regulatory elements that regulate gene expression and splicing of their cognate coding gene targets (8, 9).”
From Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder (2018) · cites this paper as [9]
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Metadata
- Authors
- Visel, A., Rubin, E. M., & Pennacchio, L. A.
- Affiliations
- Lawrence Berkeley National Laboratory (US)
- Venue
- Nature
- Published
- 2009-09
- Volume
- 461
- Issue
- 7261
- Pages
- 199-205
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2923221
- OpenAlex
- W2048263136
- Cited by
- 610
- References
- 123
- Citations by year
- 2026: 8 · 2025: 18 · 2024: 16 · 2023: 26 · 2022: 37 · 2021: 30 · 2020: 36 · 2019: 39 · 2018: 30 · 2017: 34 · 2016: 39 · 2015: 49 · 2014: 48 · 2013: 49 · 2012: 55
- FWCI
- 3.85
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Heart, Lung, and Blood Institute (R21HL098940, U01HL066681)
- National Human Genome Research Institute (R01HG003988)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Keywords
- enhancers, enhancer function, genome-wide association study, disease susceptibility, human disease genetics
- MeSH terms
- Animals, Enhancer Elements, Genetic, Gene Expression Regulation, Humans, Genome, Human, Evolution, Molecular, Genetic Predisposition to Disease, Genomics
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