Search

Parkinson disease/genetics
 
Advanced search
Browse by...
Refine your research by the most used items
Deposit
Highlights
More informations
Show items per page
Elements: 11
Page 1 on 1
 TitleAuthors / EditorsDate
add to browser selection
 Low disease risk in relatives of north african lrrk2 Parkinson disease patients Troiano, A R; Elbaz, A; Lohmann, E; Belarbi, S; ... Brice, A 2010
add to browser selection
 Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; ... Brice, Alexis 2010
add to browser selection
 Follow-up study of the GIGYF2 gene in French families with Parkinson's disease Lesage, Suzanne; Condroyer, Christel; Lohman, Ebba; Troiano, André; ... Brice, Alexis 2010
add to browser selection
 Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease Lesage, Suzanne; Anheim, Mathieu; Condroyer, Christel; Pollak, Pierre; ... Brice, Alexis 2011
add to browser selection
 VPS35 mutations in Parkinson disease Vilariño-Güell, Carles; Wider, Christian; Ross, Owen A; Dachsel, Justus C; ... Farrer, Matthew J 2011
add to browser selection
 A two-stage meta-analysis identifies several new loci for Parkinson's disease French Parkinson's Disease Genetics Study Group 2011
add to browser selection
 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Nalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; ... Wood, Nicholas W 2011
add to browser selection
 Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 2011
add to browser selection
 Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers Anheim, M; Elbaz, A; Lesage, S; Durr, A; ... Brice, A 2012
add to browser selection
 Large-scale replication and heterogeneity in Parkinson disease genetic loci Sharma, Manu 2012
add to browser selection
 The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe 2013