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	Title	Authors / Editors	Date
unige:19175	Are parkin patients particularly suited for deep-brain stimulation?	Lohmann, Ebba; Welter, Marie-Laure; Fraix, Valerie; Krack, Paul; ... Brice, Alexis	2008
unige:19747	Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia	Clot, Fabienne; Grabli, David; Cazeneuve, Cecile; Roze, Emmanuel; ... Brice, Alexis	2009
unige:45179	Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms	Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis	2009
unige:32884	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
unige:45246	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
unige:37956	SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia	Marelli, Cecilia; van de Leemput, Joyce; Johnson, Janel O; Tison, Francois; ... Brice, Alexis	2011
unige:32871	Screening of the THAP1 gene in patients with early-onset dystonia: myoclonic jerks are part of the dystonia 6 phenotype	Clot, Fabienne; Grabli, David; Burbaud, Pierre; Aya, Magali; ... Brice, Alexis	2011
unige:32873	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
unige:32874	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
unige:45211	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
unige:32814	PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population	Méneret, Aurélie; Grabli, David; Depienne, Christel; Gaudebout, Cécile; ... Roze, Emmanuel	2012
unige:33238	FXTAS: new insights and the need for revised diagnostic criteria	Apartis, Emmanuelle; Blancher, Anne; Meissner, Wassilios G; Guyant-Maréchal, Lucie; ... Anheim, Mathieu	2012
unige:45192	EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?	Lesage, Suzanne; Condroyer, Christel; Klebe, Stephan; Lohmann, Ebba; ... Brice, Alexis	2012
unige:45200	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
unige:33603	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
unige:45249	A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease	Holmans, Peter; Moskvina, Valentina; Jones, Lesley; Sharma, Manu; ... Morris, Huw R	2013
unige:130016	Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms	Huin, Vincent; Barbier, Mathieu; Bottani, Armand; Lobrinus, Johannes Alexander; ... Le Ber, Isabelle	2020

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