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Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson’s disease on chromosome 7p15.3

  • Published:2017-04-08 Issue:3 Volume:18 Page:121-133
  • ISSN:1364-6745
  • Container-title:neurogenetics
  • language:en
  • Short-container-title:Neurogenetics

Author:

Murthy Megha N., ,Blauwendraat Cornelis,Guelfi Sebastian,Hardy John,Lewis Patrick A.,Trabzuni Daniah,

Funder

Medical Research Council

Michael J. Fox Foundation for Parkinson’s Research

King Faisal Specialist Hospital and Research Centre

Department of Science and Technology, Ministry of Science and Technology

Newton Fund

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Reference36 articles.

1. Lees AJ, Hardy J, Revesz T (2009) Parkinson’s disease. Lancet 373(9680):2055–2066. doi: 10.1016/S0140-6736(09)60492-X

2. Westra HJ, Franke L (2014) From genome to function by studying eQTLs. Biochim Biophys Acta 1842(10):1896–1902. doi: 10.1016/j.bbadis.2014.04.024

3. Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, Stefansson H, Liu X, Pliner H, Lee JH, Cheng R, International Parkinson’s Disease Genomics C, Parkinson’s Study Group Parkinson’s Research: The Organized GI, andMe, GenePd, NeuroGenetics Research C, Hussman Institute of Human G, Ashkenazi Jewish Dataset I, Cohorts for H, Aging Research in Genetic E, North American Brain Expression C, United Kingdom Brain Expression C, Greek Parkinson’s Disease C, Alzheimer Genetic Analysis G, Ikram MA, Ioannidis JP, Hadjigeorgiou GM, Bis JC, Martinez M, Perlmutter JS, Goate A, Marder K, Fiske B, Sutherland M, Xiromerisiou G, Myers RH, Clark LN, Stefansson K, Hardy JA, Heutink P, Chen H, Wood NW, Houlden H, Payami H, Brice A, Scott WK, Gasser T, Bertram L, Eriksson N, Foroud T, Singleton AB (2014) Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease. Nat Genet 46(9):989–993. doi: 10.1038/ng.3043

4. Trabzuni D, Ryten M, Emmett W, Ramasamy A, Lackner KJ, Zeller T, Walker R, Smith C, Lewis PA, Mamais A, de Silva R, Vandrovcova J, International Parkinson Disease Genomics C, Hernandez D, Nalls MA, Sharma M, Garnier S, Lesage S, Simon-Sanchez J, Gasser T, Heutink P, Brice A, Singleton A, Cai H, Schadt E, Wood NW, Bandopadhyay R, Weale ME, Hardy J, Plagnol V (2013) Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. PLoS One 8(8):e70724. doi: 10.1371/journal.pone.0070724

5. Yu CH, Pal LR, Moult J (2016) Consensus genome-wide expression quantitative trait loci and their relationship with human complex trait disease. OMICS 20(7):400–414. doi: 10.1089/omi.2016.0063
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