Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Author(s) -
Margaux F. Keller,
Mohamad Saad,
José Brás,
Francesco Bettella,
Nayia Nicolaou,
Javier SimónSánchez,
Florian Mittag,
Finja Büchel,
Manu Sharma,
J. Raphael Gibbs,
Joshua Shulman,
Valentina Moskvina,
Alexandra Dürr,
Peter Holmans,
Laura L. Kilarski,
Rita Guerreiro,
D. G. Hernandez,
Alexis Brice,
Pauli Ylikotila,
Hreinn Stefánsson,
Kari Majamaa,
Huw R. Morris,
N. Williams,
Thomas Gasser,
Peter Heutink,
Nicholas Wood,
John Hardy,
María Martínez,
Andrew Singleton,
Mike A. Nalls
Publication year - 2013
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/ddt030
Subject(s) - biology , missing heritability problem , heritability , trait , parkinson's disease , genetics , genome wide association study , disease , quantitative trait locus , genome , computational biology , evolutionary biology , gene , single nucleotide polymorphism , genotype , computer science , medicine , programming language
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