Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

M.F. Keller, M. Saad, J. Bras, F. Bettella, N. Nicolaou, J. Simon-Sanchez, F. Mittag, F. Buchel, M. Sharma, J.R. Gibbs, C. Schulte, V. Moskvina, A. Durr, P. Holmans, L.L. Kilarski, R. Guerreiro, D.G. Hernandez, A. Brice, P. Ylikotila, H. StefanssonK. Majamaa, H.R. Morris, N. Williams, T. Gasser, P. Heutink, N.W. Wood, J. Hardy, M. Martinez, A.B. Singleton, M.A. Nalls

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)4996-5009
JournalHuman Molecular Genetics
Volume21
Issue number22
DOIs
Publication statusPublished - 2012

Cite this

Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simon-Sanchez, J., ... Nalls, M. A. (2012). Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics, 21(22), 4996-5009. https://doi.org/10.1093/hmg/dds335