Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control studyOwen A. Ross, Hiroyuki Tomiyama, Alexandra I. Soto‐Ortolaza et al.|The Lancet Neurology|2011Cited by 344
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European populationMohamad Saad, Peter A. Silburn, Christophe Tzourio et al.|Human Molecular Genetics|2010Cited by 161
Large-scale replication and heterogeneity in Parkinson disease genetic lociManu Sharma, Kuo-Chu Yueh, John P. A. Ioannidis et al.|Neurology|2012Cited by 132
A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variantsManu Sharma, Eng King Tan, John P. A. Ioannidis et al.|Journal of Medical Genetics|2012Cited by 107
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's diseaseRejko Krüger, Demetrius M. Maraganore, Manu Sharma et al.|Neurobiology of Aging|2009Cited by 73