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Title

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Authors
Nalls, Michael A
Plagnol, Vincent
Hernandez, Dena G
Sharma, Manu
Sheerin, Una-Marie
Saad, Mohamad
Simón-Sánchez, J
Schulte, Claudia
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CollaborationWith : Pollak, Pierre
Published in The Lancet. 2011, vol. 377, no. 9766, p. 641-9
Abstract Genome-wide association studies (GWAS) for Parkinson's disease have linked two loci (MAPT and SNCA) to risk of Parkinson's disease. We aimed to identify novel risk loci for Parkinson's disease.
Keywords AdultAge of OnsetAgedAllelesFemaleGenetic Loci/geneticsGenetic Predisposition to Disease/geneticsGenetic Variation/geneticsGenome-Wide Association StudyGenotypeHumansMaleMiddle AgedParkinson Disease/geneticsPolymorphism, Single Nucleotide/geneticsRisk AssessmentSequence Analysis
Identifiers
PMID: 21292315
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Article (Published version) (743 Kb) - public document Free access
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Research group Maladie de Parkinson (911)
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NALLS, Michael A et al. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. In: The Lancet, 2011, vol. 377, n° 9766, p. 641-9. https://archive-ouverte.unige.ch/unige:45211

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Deposited on : 2015-01-14

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