Scientific article
Meta-analysis
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
ContributorsNalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; Sheerin, Una-Marie; Saad, Mohamad; Simón-Sánchez, J; Schulte, Claudia; Lesage, Suzanne; Sveinbjörnsdóttir, Sigurlaug; Stefánsson, Kári; Martinez, Maria; Hardy, John; Heutink, Peter; Brice, Alexis; Gasser, Thomas; Singleton, Andrew B; Wood, Nicholas W; International Parkinson Disease Genomics Consortium
CollaboratorsPollak, Pierre
Published inLancet, vol. 377, no. 9766, p. 641-649
Publication date2011
Abstract
Keywords
- Adult
- Age of Onset
- Aged
- Alleles
- Female
- Genetic Loci/genetics
- Genetic Predisposition to Disease/genetics
- Genetic Variation/genetics
- Genome-Wide Association Study
- Genotype
- Humans
- Male
- Middle Aged
- Parkinson Disease/genetics
- Polymorphism, Single Nucleotide/genetics
- Risk Assessment
- Sequence Analysis
Affiliation entities
Research groups
Citation (ISO format)
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: Lancet, 2011, vol. 377, n° 9766, p. 641–649. doi: 10.1016/S0140-6736(10)62345-8
Main files (1)
Article (Published version)
Identifiers
- PID : unige:45211
- DOI : 10.1016/S0140-6736(10)62345-8
- PMID : 21292315
Journal ISSN0140-6736
