| Title | Authors / Editors | Date |
unige:160766 |
A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33 |
Baulac, Stéphane; Gourfinkel-An, Isabelle; Picard, Fabienne; Rosenberg-Bourgin, Myriam; ... LeGuern, Eric |
1999 |
unige:160756 |
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31 |
Baulac, Stéphanie; Picard, Fabienne; Herman, Alexandra; Feingold, Josué; ... LeGuern, Eric |
2001 |
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: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: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: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: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: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: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 |