Browsing by Author Singleton, Andrew
Results 1 to 9 of 9
| Issue Date | Title | Author(s) | Type | Access |
|---|---|---|---|---|
| 2008 | Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3 | Okubadejo, Njideka; Britton, Angela; Crews, Cynthia; Akinyemi, Rufus; Hardy, John ; Singleton, Andrew ; Brás, José | article | openAccess |
| 2008 | Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2 | Brás, José ; Guerreiro, Rita ; Ribeiro, Maria ; Morgadinho, Ana ; Januário, Cristina ; Dias, Margarida ; Calado, Ana ; Semedo, Cristina ; Oliveira, Catarina ; Hardy, John ; Singleton, Andrew | article | openAccess |
| 2006 | Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort | Guerreiro, Rita J. ; Brás, José M. ; Santana, Isabel ; Januário, Cristina ; Santiago, Beatriz ; Morgadinho, Ana S. ; Ribeiro, Maria H. ; Hardy, John ; Singleton, Andrew ; Oliveira, Catarina | article | openAccess |
| 1-Sep-2008 | Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal | Brás, José ; Paisan-Ruiz, Coro ; Guerreiro, Rita ; Ribeiro, Maria Helena ; Morgadinho, Ana ; Januário, Cristina ; Sidransky, Ellen ; Oliveira, Catarina ; Singleton, Andrew | article | openAccess |
| 2005 | G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort | Brás, José Miguel ; Guerreiro, Rita João ; Ribeiro, Maria Helena ; Januário, Cristina ; Morgadinho, Ana ; Oliveira, Catarina Resende ; Cunha, Luís ; Hardy, John ; Singleton, Andrew | article | openAccess |
| 2010 | Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP | Guerreiro, 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 | article | openAccess |
| 3-Mar-2010 | Genetic Variability in CLU and Its Association with Alzheimer's Disease | Guerreiro, 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 | article | openAccess |
| 2013 | NOTCH3 variants and risk of ischemic stroke | Ross, 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. | article | openAccess |
| 11-Jun-2008 | TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis | Guerreiro, Rita ; Schymick, Jennifer C.; Crews, Cynthia; Singleton, Andrew ; Hardy, John ; Traynor, Bryan J. | article | openAccess |