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Name
Singleton, Andrew
 
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Publications
(Todas)

Resultados 1-9 de 9.

Data de publicaçãoTítuloAutor(es)TipoAcesso
12008Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3Okubadejo, Njideka; Britton, Angela; Crews, Cynthia; Akinyemi, Rufus; Hardy, John ; Singleton, Andrew ; Brás, José articleopenAccess
22008Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2Brás, José ; Guerreiro, Rita ; Ribeiro, Maria ; Morgadinho, Ana ; Januário, Cristina ; Dias, Margarida ; Calado, Ana ; Semedo, Cristina ; Oliveira, Catarina ; Hardy, John ; Singleton, Andrew articleopenAccess
32006Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohortGuerreiro, Rita J. ; Brás, José M. ; Santana, Isabel ; Januário, Cristina ; Santiago, Beatriz ; Morgadinho, Ana S. ; Ribeiro, Maria H. ; Hardy, John ; Singleton, Andrew ; Oliveira, Catarina articleopenAccess
41-Set-2008Complete screening for glucocerebrosidase mutations in Parkinson disease patients from PortugalBrás, José ; Paisan-Ruiz, Coro ; Guerreiro, Rita ; Ribeiro, Maria Helena ; Morgadinho, Ana ; Januário, Cristina ; Sidransky, Ellen ; Oliveira, Catarina ; Singleton, Andrew articleopenAccess
52005G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohortBrás, José Miguel ; Guerreiro, Rita João ; Ribeiro, Maria Helena ; Januário, Cristina ; Morgadinho, Ana ; Oliveira, Catarina Resende ; Cunha, Luís ; Hardy, John ; Singleton, Andrew articleopenAccess
62010Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APPGuerreiro, Rita João ; Baquero, Miquel ; Blesa, Rafael ; Boada, Mercè ; Brás, José Miguel ; Bullido, Maria. J. ; Calado, Ana ; Crook, Richard ; Ferreira, Carla; Frank, Ana ; Gómez-Isla, Teresa ; Hernández, Isabel ; Lleó, Alberto ; Machado, Álvaro ; Martínez- Lage, Pablo ; Masdeu, José ; Molina-Porcel, Laura ; Molinuevo, José L. ; Pastor, Pau ; Pérez-Tur, Jordi ; Relvas, Rute ; Oliveira, Catarina Resende ; Ribeiro, Maria Helena ; Rogaeva, Ekaterina ; Sá, Alfredo ; Samaranch, Lluís ; Sánchez-Valle, Raquel ; Santana, Isabel ; Tàrraga, Lluís ; Valdivieso, Fernando ; Singleton, Andrew ; Hardy, John ; Clarimón, Jordi articleopenAccess
73-Mar-2010Genetic Variability in CLU and Its Association with Alzheimer's DiseaseGuerreiro, Rita J. ; Beck, John ; Gibbs, J. Raphael ; Santana, Isabel ; Rossor, Martin N. ; Schott, Jonathan M. ; Nalls, Michael A. ; Ribeiro, Helena ; Santiago, Beatriz ; Fox, Nick C. ; Oliveira, Catarina ; Collinge, John ; Mead, Simon ; Singleton, Andrew ; Hardy, John articleopenAccess
82013NOTCH3 variants and risk of ischemic strokeRoss, Owen A.; Soto-Ortolaza, Alexandra I.; Heckman, Michael G.; Verbeeck, Christophe; Serie, Daniel J.; Rayaprolu, Sruti; Rich, Stephen S.; Nalls, Michael A. ; Singleton, Andrew ; Guerreiro, Rita ; Kinsella, Emma; Wszolek, Zbigniew K.; Brott, Thomas G.; Brown, Robert D.; Worrall, Bradford B.; Meschia, James F.articleopenAccess
911-Jun-2008TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosisGuerreiro, Rita ; Schymick, Jennifer C.; Crews, Cynthia; Singleton, Andrew ; Hardy, John ; Traynor, Bryan J. articleopenAccess