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Article type: Article Commentary
Authors: Coetzee, Gerhard A.; * | Pierce, Steven
Affiliations: Van Andel Research Institute, Grand Rapids, MI, USA
Correspondence: [*] Correspondence to: Dr. G.A. Coetzee, Van Andel Research Institute, 333 Bostwick Ave., N.E., Grand Rapids, MI 49503, USA. E-mail: [email protected].
Abstract: Genome-wide association studies of Parkinson’s disease have revealed polymorphic variants associated with closely mapped genes of interest. We propose here that those genes may only represent the tip of an iceberg of regulatory effects and do not necessary reflect disease relevance. To usefully interpret a risk locus, one needs to consider 5 dimensions of information, which represent the three-dimensional structure of chromatin (dimensions #1– 3), which is locally variable across time (dimension #4), and, most importantly, dependent on cell type and context (dimension #5).
Keywords: GWAS, enhancer, non-coding DNA, chromatin
DOI: 10.3233/JPD-171256
Journal: Journal of Parkinson's Disease, vol. 8, no. 1, pp. 13-15, 2018
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