Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
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Open Access
- 2 February 2011
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 377 (9766) , 641-649
- https://doi.org/10.1016/s0140-6736(10)62345-8
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Genome-wide association study confirms extant PD risk loci among the DutchEuropean Journal of Human Genetics, 2011
- Towards a complete resolution of the genetic architecture of diseaseTrends in Genetics, 2010
- Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's diseaseNature Genetics, 2010
- Genome-wide association study reveals genetic risk underlying Parkinson's diseaseNature Genetics, 2009
- Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's DiseaseNew England Journal of Medicine, 2009
- Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibilityProceedings of the National Academy of Sciences, 2009
- Whole-genome association study identifies STK39 as a hypertension susceptibility geneProceedings of the National Academy of Sciences, 2009
- Genomewide association study for susceptibility genes contributing to familial Parkinson diseaseHuman Genetics, 2008
- The NCBI dbGaP database of genotypes and phenotypesNature Genetics, 2007
- Overcoming the Winner’s Curse: Estimating Penetrance Parameters from Case-Control DataAmerican Journal of Human Genetics, 2007