Lack of association between p.Ser167Asn variant of Parkin and Parkinson's disease: A meta-analysis of 15 studies involving 2,280 cases and 2,459 controls

Association of GWAS loci with PD in China

(2011) Xue-Li Chang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

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

(2011)   LANCET

Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control

(2009) J Brooks et al.   JOURNAL OF MEDICAL GENETICS

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

(2009) Wataru Satake et al.   NATURE GENETICS

Genome-wide association study reveals genetic risk underlying Parkinson's disease

(2009) Javier Simón-Sánchez et al.   NATURE GENETICS

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

(2009) N. Pankratz et al.   NEUROLOGY

PARKIN-coding polymorphisms are not associated with Parkinson's disease in a population from northeastern Mexico

(2009) Héctor R. Martínez et al.   NEUROSCIENCE LETTERS

Low frequency of the PARK2 gene mutations in Polish patients with the early-onset form of Parkinson disease

(2009) Dariusz Koziorowski et al.   PARKINSONISM & RELATED DISORDERS

Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients

(2008) Patricia de Carvalho Aguiar et al.   MOVEMENT DISORDERS

A multidisciplinary study of patients with early-onset PD with and without parkin mutations

(2008) E. Lohmann et al.   NEUROLOGY

Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3

(2008) Njideka Okubadejo et al.   PLoS One