Parkinson hastalığı genetiğinin genişletilmesi: yeni risk lokusu, genomik bağlam, nedensel içgörüler ve kalıtsal risk

Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk

Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D, Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Pihlstrom L, Siitonen A, Iwaki H, Leonard H, Faghri F, Raphael Gibbs J, Hernandez DG, Scholz SW, Botia JA, Martinez M, Corvol J, Lesage S, Jankovic J, Shulman LM, The 23andMe Research Team, System Genomics of Parkinson’s Disease (SGPD) Consortium, Sutherland M, Tienari P, Majamaa K, Toft M, Andreassen OA, Bangale T, Brice A, Yang J, Gan-Or Z, Gasser T, Heutink P, Shulman JM, Wood N, Hinds DA, Hardy JA, Morris HR, Gratten J, Visscher PM, Graham RR, Singleton AB, for the International Parkinson’s Disease Genomics Consortium.

· 2018-08-09

DOI: 10.1101/388165