Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Author(s) -
M. F. Keller,
M. Saad,
J. Bras,
F. Bettella,
N. Nicolaou,
Javier SimónSánchez,
Florian Mittag,
F. B. chel,
Manoj B. Sharma,
J. Raphael Gibbs,
Claudia Schulte,
V. Moskvina,
A. Durr,
P. Holmans,
Laura L. Kilarski,
R. Guerreiro,
D. G. Hernandez,
Alexis Brice,
P. Ylikotila,
H. Stefánsson,
Kari Majamaa,
Huw R. Morris,
N. Williams,
T. Gasser,
P. Heutink,
Nicholas Wood,
John Hardy,
Madison J Martinez,
Andrew Singleton,
M. 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/ddt199
Subject(s) - biology , heritability , missing heritability problem , trait , genetics , genome wide association study , quantitative trait locus , disease , genome , computational biology , evolutionary biology , gene , single nucleotide polymorphism , genotype , computer science , medicine , programming language
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