A
André R. Troiano
Researcher at French Institute of Health and Medical Research
Publications - 8
Citations - 1856
André R. Troiano is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Gene & Penetrance. The author has an hindex of 7, co-authored 8 publications receiving 1578 citations. Previous affiliations of André R. Troiano include Pierre-and-Marie-Curie University & University of Paris.
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Journal ArticleDOI
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Ellen Sidransky,Mike A. Nalls,Jan O. Aasly,Judith Aharon-Peretz,Grazia Annesi,Egberto Reis Barbosa,Anat Bar-Shira,Daniela Berg,Jose Bras,Jose Bras,Alexis Brice,Alexis Brice,Chiung-Mei Chen,Lorraine N. Clark,Christel Condroyer,Elvira Valeria De Marco,Alexandra Durr,Alexandra Durr,Michael J. Eblan,Stanley Fahn,Matthew J. Farrer,Hon-Chung Fung,Ziv Gan-Or,Thomas Gasser,Ruth Gershoni-Baruch,Ruth Gershoni-Baruch,Nir Giladi,Nir Giladi,Alida Griffith,Tanya Gurevich,Tanya Gurevich,Cristina Januário,Peter Kropp,Anthony E. Lang,Guey Jen Lee-Chen,Suzanne Lesage,Karen Marder,Ignacio F. Mata,Anat Mirelman,Jun Mitsui,Ikuko Mizuta,Giuseppe Nicoletti,Giuseppe Nicoletti,Catarina R. Oliveira,Ruth Ottman,Avi Orr-Urtreger,Lygia da Veiga Pereira,Aldo Quattrone,Aldo Quattrone,Ekaterina Rogaeva,Arndt Rolfs,Hanna Rosenbaum,Roberto Rozenberg,Ali Samii,Ali Samii,Ali Samii,Ted Samaddar,Claudia Schulte,Manu Sharma,Manu Sharma,Andrew B. Singleton,Andrew B. Singleton,Mariana Spitz,Mariana Spitz,Eng-King Tan,Eng-King Tan,Nahid Tayebi,Tatsushi Toda,André R. Troiano,Shoji Tsuji,Matthias Wittstock,Tyra G. Wolfsberg,Yih-Ru Wu,Cyrus P. Zabetian,Yi Zhao,Shira G. Ziegler +75 more
TL;DR: Data collected demonstrate that there is a strong association between GBA mutations and Parkinson's disease, and those with a GBA mutation presented earlier with the disease, were more likely to have affected relatives, and were morelikely to have atypical clinical manifestations.
Journal ArticleDOI
Molecular analyses of the LRRK2 gene in European and North-African autosomal dominant Parkinson’s disease
Suzanne Lesage,Christel Condroyer,Annie Lannuzel,Ebba Lohmann,André R. Troiano,François Tison,P. Damier,Stéphane Thobois,Anne-Marie Ouvrard-Hernandez,Sophie Rivaud-Péchoux,Christine Brefel-Courbon,Alain Destée,Christine Tranchant,Marc Romana,Laurence Leclere,Alexandra Durr,Alexis Brice +16 more
TL;DR: It is concluded that LRRK2 mutations are a common cause of autosomal dominant Parkinson’s disease in Europe and North Africa.
Journal ArticleDOI
Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease
Suzanne Lesage,Soreya Belarbi,André R. Troiano,Christel Condroyer,Nassima Hecham,Pierre Pollak,Ebba Lohman,Traki Benhassine,F. Ysmail-Dahlouk,Alexandra Durr,Meriem Tazir,Alexis Brice +11 more
TL;DR: It was found that dyskinesias were significantly more frequent in patients with the G2019S mutation than in noncarriers, and in ethnically matched healthy controls.
Journal Article
A-SYNUCLEIN GENE DUPLICATION IS PRESENT IN SPORADIC PARKINSON DISEASE. Authors' reply
N. Brueggemann,P. Odin,A. Gruenewald,Vera Tadic,J. Hagenah,Günter Seidel,Katja Lohmann,Cliff S. Klein,Ana Djarmati,Beam S. Jeon,Tele-Beom Ahn,Sung S. Park,André R. Troiano,Cécile Cazeneuve,I. Le Ber,A. M. Bonnet,Suzanne Lesage,Alexis Brice,Beom S. Jeon,Tae B. Ahn +19 more