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 TitleAuthors / EditorsDate
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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
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EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? Lesage, Suzanne; Condroyer, Christel; Klebe, Stephan; Lohmann, Ebba; ... Brice, Alexis 2012
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Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities Mittag, Florian; Büchel, Finja; Saad, Mohamad; Jahn, Andreas; ... Sharma, Manu 2012
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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population Saad, Mohamad; Lesage, Suzanne; Saint-Pierre, Aude; Corvol, Jean-Christophe; ... Brice, Alexis 2011
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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
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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
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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
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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
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Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis 2009
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Are parkin patients particularly suited for deep-brain stimulation? Lohmann, Ebba; Welter, Marie-Laure; Fraix, Valerie; Krack, Paul; ... Brice, Alexis 2008