KELLER, M.F, SAAD, M, BRAS, J, BETTELLA, F, NICOLAOU, N, SIMÓN-SÁNCHEZ, J, MITTAG, F, BÜCHEL, F, SHARMA, M, GIBBS, J.R, SCHULTE, C, MOSKVINA, V, DURR, A, HOLMANS, P, KILARSKI, L.L, GUERREIRO, R, HERNANDEZ, D.G, BRICE, A, YLIKOTILA, P, STEFÁNSSON, H, MAJAMAA, K, MORRIS, H.R, WILLIAMS, N, GASSER, T, HEUTINK, P, WOOD, N.W, HARDY, J, MARTINEZ, M, SINGLETON, A.B, NALLS, M.A, the INTERNATIONAL PARKINSON'S DISEASE GENOMICS CONSORTIUM (IPDGC) and the WELLCOME TRUST CASE CONTROL CONSORTIUM.
(2012)
Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.
Human Molecular Genetics, 21(22), 4996-5009.