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. 2013 Feb 14;22(8):1696. doi: 10.1093/hmg/ddt030

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

Margaux F Keller, Mohamad Saad, Jose Bras, Francesco Bettella, Nayia Nicolaou, Javier Simón-Sánchez, Florian Mittag, Finja Büchel, Manu Sharma, J Raphael Gibbs, Claudia Schulte, Valentina Moskvina, Alexandra Durr, Peter Holmans, Laura L Kilarski, Rita Guerreiro, Dena G Hernandez, Alexis Brice, Pauli Ylikotila, Hreinn Stefánsson, Kari Majamaa, Huw R Morris, Nigel Williams, Thomas Gasser, Peter Heutink, Nicholas W Wood, John Hardy, Maria Martinez, Andrew B Singleton, Michael A Nalls; for the International Parkinson's Disease Genomics Consortium (IPDGC) and The Wellcome Trust Case Control Consortium 2 (WTCCC2)
PMCID: PMC3605835

Human Molecular Genetics 2012 21:22; pp. 4996–5009; doi: 10.1093/hmg/dds335

This paper is now published as Open Access.

FUNDING

Funding to pay the Open Access publication charges for this article was provided by the NIH Public Access Policy, Division G, Title II, Section 218 of PL 110-161.

Articles from Human Molecular Genetics are provided here courtesy of Oxford University Press

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