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The Parkinson's Disease Genome‐Wide Association Study Locus Browser
25 auth. F. P. Grenn, J. Kim, Mary B Makarious, H. Iwaki, A. Illarionova, K. Brolin, Jillian H. Kluss, A. Schumacher-Schuh, H. Leonard, F. Faghri, Kimberley J. Billingsley, L. Krohn, Ashley Hall, M. Diez-Fairen, M. T. Periñán, ... J. Foo, C. Sandor, C. Webber, B. Fiske, J. R. Gibbs, M. Nalls, A. Singleton, S. Bandres-Ciga, X. Reed, C. Blauwendraat
Parkinson's disease (PD) is a neurodegenerative disease with an often complex component identifiable by genome‐wide association studies. The most recent large‐scale PD genome‐wide association studies have identified more than 90 independent risk var…
Parkinson's disease (PD) is a neurodegenerative disease with an often complex component identifiable by genome‐wide association studies. The most recent large‐scale PD genome‐wide association studies have identified more than 90 independent risk variants for PD risk and progression across more than 80 genomic regions. One major challenge in current genomics is the identification of the causal gene(s) and variant(s) at each genome‐wide association study locus. The objective of the current study was to create a tool that would display data for relevant PD risk loci and provide guidance with the prioritization of causal genes and potential mechanisms at each locus.
Published in Movement Disorders
18
6 2020