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2015
Mark Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.
Ogaki, Kotaro ; Koga, Shunsuke ; Heckman, Michael G ; Fiesel, Fabienne C ; Ando, Maya ; Labbé, Catherine ; Lorenzo-Betancor, Oswaldo ; Moussaud-Lamodière, Elisabeth L ; Soto-Ortolaza, Alexandra I and Walton, Ronald L , et al. (2015) In Neurology
- Contribution to journal › Article
Mark Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.
Labbé, Catherine ; Ogaki, Kotaro ; Lorenzo-Betancor, Oswaldo ; Soto-Ortolaza, Alexandra I ; Walton, Ronald L ; Rayaprolu, Sruti ; Fujioka, Shinsuke ; Murray, Melissa E ; Heckman, Michael G and Puschmann, Andreas ^LU , et al. (2015) In Neurology 85(19). p.1680-1686
- Contribution to journal › Article
2014
Mark Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
Heckman, Michael G. ; Elbaz, Alexis ; Soto-Ortolaza, Alexandra I. ; Serie, Daniel J ; Aasly, Jan O. ; Annesi, Grazia ; Auburger, Georg ; Bacon, Justin A. ; Boczarska-Jedynak, Magdalena and Bozi, Maria , et al. (2014) In Neurobiology of Aging 35(1). p.5-266
- Contribution to journal › Article
2013
Mark Population-specific Frequencies for LRRK2 Susceptibility Variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium
Heckman, Michael G. ; Soto-Ortolaza, Alexandra I. ; Aasly, Jan O. ; Abahuni, Nadine ; Annesi, Grazia ; Bacon, Justin A. ; Bardien, Soraya ; Bozi, Maria ; Brice, Alexis and Brighina, Laura , et al. (2013) In Movement Disorders 28(12). p.1740-1744
- Contribution to journal › Article
2011
Mark Human leukocyte antigen variation and Parkinson's disease.
Puschmann, Andreas ^LU ; Verbeeck, Christophe ; Heckman, Michael G ; Soto-Ortolaza, Alexandra I ; Lynch, Timothy ; Jasinska-Myga, Barbara ; Opala, Grzegorz ; Krygowska-Wajs, Anna ; Barcikowska, Maria and Uitti, Ryan J , et al. (2011) In Parkinsonism & Related Disorders 17. p.376-378
- Contribution to journal › Article
Mark VPS35 Mutations in Parkinson Disease
Vilarino-Gueell, Carles ; Wider, Christian ; Ross, Owen A. ; Dachsel, Justus C. ; Kachergus, Jennifer M. ; Lincoln, Sarah J. ; Soto-Ortolaza, Alexandra I. ; Cobb, Stephanie A. ; Wilhoite, Greggory J. and Bacon, Justin A. , et al. (2011) In American Journal of Human Genetics 89(1). p.162-167
- Contribution to journal › Article
Mark Independent and Joint Effects of the MAPT and SNCA Genes in Parkinson Disease
Elbaz, Alexis ; Ross, Owen A. ; Ioannidis, John P. A. ; Soto-Ortolaza, Alexandra I. ; Moisan, Frederic ; Aasly, Jan ; Annesi, Grazia ; Bozi, Maria ; Brighina, Laura and Chartier-Harlin, Marie-Christine , et al. (2011) In Annals of Neurology 69(5). p.778-792
- Contribution to journal › Article
Mark Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
Ross, Owen A. ; Soto-Ortolaza, Alexandra I. ; Heckman, Michael G. ; Aasly, Jan O. ; Abahuni, Nadine ; Annesi, Grazia ; Bacon, Justin A. ; Bardien, Soraya ; Bozi, Maria and Brice, Alexis , et al. (2011) In Lancet Neurology 10(10). p.898-908
- Contribution to journal › Article
2010
Mark LRRK2 variation and Parkinson's disease in African Americans
Ross, Owen A. ; Wilhoite, Greggory J. ; Bacon, Justin A. ; Soto-Ortolaza, Alexandra I. ; Kachergus, Jennifer ; Cobb, Stephanie A ; Puschmann, Andreas ^LU ; Vilariño-Güell, Carles ; Farrer, Matthew J. and Graff-Radford, Neill R , et al. (2010) In Movement Disorders 25(12). p.1973-1992
- Contribution to journal › Article

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