S
Simone Van De Loo
Researcher at Goethe University Frankfurt
Publications - 3
Citations - 415
Simone Van De Loo is an academic researcher from Goethe University Frankfurt. The author has contributed to research in topics: Genome-wide association study & Genetic epidemiology. The author has an hindex of 3, co-authored 3 publications receiving 376 citations.
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Journal ArticleDOI
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.
Owen A. Ross,Alexandra I. Soto-Ortolaza,Michael G. Heckman,Jan O. Aasly,Nadine Abahuni,Grazia Annesi,Justin A. Bacon,Soraya Bardien,Maria Bozi,Alexis Brice,Laura Brighina,Christine Van Broeckhoven,Christine Van Broeckhoven,Jonathan Carr,Marie-Christine Chartier-Harlin,Marie-Christine Chartier-Harlin,Efthimios Dardiotis,Efthimios Dardiotis,Dennis W. Dickson,Nancy N. Diehl,Alexis Elbaz,Alexis Elbaz,Carlo Ferrarese,Alessandro Ferraris,Brian K. Fiske,J. Mark Gibson,Rachel A. Gibson,Georgios M. Hadjigeorgiou,Georgios M. Hadjigeorgiou,Nobutaka Hattori,John P. A. Ioannidis,John P. A. Ioannidis,Barbara Jasinska-Myga,Beom S. Jeon,Yun Joong Kim,Christine Klein,Rejko Krüger,Elli Kyratzi,Suzanne Lesage,Suzanne Lesage,Suzanne Lesage,Chin-Hsien Lin,Timothy Lynch,Demetrius M. Maraganore,George D. Mellick,Eugénie Mutez,Eugénie Mutez,Christer Nilsson,Grzegorz Opala,Sung Sup Park,Andreas Puschmann,Aldo Quattrone,Manu Sharma,Peter A. Silburn,Young H. Sohn,Leonidas Stefanis,Vera Tadic,Jessie Theuns,Jessie Theuns,Hiroyuki Tomiyama,Ryan J. Uitti,Enza Maria Valente,Simone Van De Loo,Demetrios K. Vassilatis,Carles Vilariño-Güell,Linda R. White,Karin Wirdefeldt,Zbigniew K. Wszolek,Ruey-Meei Wu,Matthew J. Farrer,Matthew J. Farrer +70 more
TL;DR: The results for LRRK2 show that several rare and common genetic variants in the same gene can have independent effects on disease risk, and are important in the cause and pathogenesis of PD in a greater proportion of patients with this disease than previously believed.
Journal ArticleDOI
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
Alexis Elbaz,Owen A. Ross,John P. A. Ioannidis,John P. A. Ioannidis,Alexandra I. Soto-Ortolaza,Frédéric Moisan,Jan O. Aasly,Grazia Annesi,Maria Bozi,Laura Brighina,Marie-Christine Chartier-Harlin,Marie-Christine Chartier-Harlin,Alain Destée,Alain Destée,Carlo Ferrarese,Alessandro Ferraris,J. Mark Gibson,Suzana Gispert,Georgios M. Hadjigeorgiou,Georgios M. Hadjigeorgiou,Barbara Jasinska-Myga,Christine Klein,Rejko Krüger,Jean-Charles Lambert,Katja Lohmann,Simone Van De Loo,Marie-Anne Loriot,Marie-Anne Loriot,Marie-Anne Loriot,Timothy Lynch,George D. Mellick,George D. Mellick,George D. Mellick,Eugénie Mutez,Eugénie Mutez,Christer Nilsson,Grzegorz Opala,Andreas Puschmann,Aldo Quattrone,Manu Sharma,Peter A. Silburn,Leonidas Stefanis,Ryan J. Uitti,Enza Maria Valente,Carles Vilariño-Güell,Carles Vilariño-Güell,Karin Wirdefeldt,Zbigniew K. Wszolek,Georgia Xiromerisiou,Georgia Xiromerisiou,Demetrius M. Maraganore,Matthew J. Farrer,Matthew J. Farrer +52 more
TL;DR: The independent and joint effects of the genes encoding alpha‐synuclein and microtubule‐associated protein tau in Parkinson disease (PD) are studied as part of a large meta‐analysis of individual data from case–control studies participating in the Genetic Epidemiology of Parkinson's Disease (GEO‐PD) consortium.
Journal ArticleDOI
Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.
Michael G. Heckman,Alexandra I. Soto-Ortolaza,Jan O. Aasly,Nadine Abahuni,Grazia Annesi,Justin A. Bacon,Soraya Bardien,Maria Bozi,Alexis Brice,Laura Brighina,Jonathan Carr,Marie-Christine Chartier-Harlin,Efthimios Dardiotis,Dennis W. Dickson,Nancy N. Diehl,Alexis Elbaz,Carlo Ferrarese,Brian K. Fiske,J. Mark Gibson,Rachel A. Gibson,Georgios M. Hadjigeorgiou,Nobutaka Hattori,John P. A. Ioannidis,Magdalena Boczarska-Jedynak,Barbara Jasinska-Myga,Beom S. Jeon,Yun Joong Kim,Christine Klein,Rejko Krüger,Elli Kyratzi,Suzanne Lesage,Suzanne Lesage,Chin-Hsien Lin,Timothy Lynch,Demetrius M. Maraganore,George D. Mellick,Eugénie Mutez,Christer Nilsson,Grzegorz Opala,Sung Sup Park,Simona Petrucci,Andreas Puschmann,Aldo Quattrone,Manu Sharma,Peter A. Silburn,Young H. Sohn,Leonidas Stefanis,Vera Tadic,Jessie Theuns,Hiroyuki Tomiyama,Ryan J. Uitti,Enza Maria Valente,Christine Van Broeckhoven,Simone Van De Loo,Demetrios K. Vassilatis,Carles Vilariño-Güell,Linda R. White,Karin Wirdefeldt,Zbigniew K. Wszolek,Ruey-Meei Wu,Fayçal Hentati,Matthew J. Farrer,Owen A. Ross +62 more
TL;DR: Leucine‐rich repeat kinase 2 variation related to disease susceptibility displays many features that reflect the nature of complex, late‐onset sporadic disorders like Parkinson's disease.