Human Molecular Genetics, 23, 3, pp. 831-41 Human Molecular Genetics, 23, 831-41 Human molecular genetics, 23(3), 831-841. Oxford University Press Human Molecular Genetics, 23(3), 831-841 Human molecular genetics 23(3), 831-841 (2013). doi:10.1093/hmg/ddt465 Human Molecular Genetics, 23(3), 831-841. Oxford University Press
Human Molecular Genetics, 21, 22, pp. 4996-5009 Keller, M F, Saad, M, Bras, J, Bettella, F, Nicolaou, N, Simon-Sanchez, J, Mittag, F, Buchel, 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, Stefansson, 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 2012, ' Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease ', Human Molecular Genetics, vol. 21, no. 22, pp. 4996-5009 . https://doi.org/10.1093/hmg/dds335 Human molecular genetics, 21(22), 4996-5009. Oxford University Press Human molecular genetics 21(22), 4996-5009 (2012). doi:10.1093/hmg/dds335 Human Molecular Genetics, 21(22), 4996-5009. Oxford University Press Human Molecular Genetics, 21, 4996-5009