Results 1 to 8 of 8
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TypeTitleAuthor(s)YearViews
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
Journal:
Nature Genetics
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.genetics.nature.com
Rogaeva, E; Meng, Y; Lee, JH; Gu, Y; Kawarai, T; Zou, F; Katayama, T; Baldwin, CT; Cheng, R; Hasegawa, H; Chen, F; Shibata, N; Lunetta, KL; PardossiPiquard, R; Bohm, C; Wakutani, Y; Cupples, LA; Cuenco, KT; Green, RC; Pinessi, L; Rainero, I; Sorbi, S; Bruni, A; Duara, R; Friedland, RP; Inzelberg, R; Hampe, W; Bujo, H; Song, YQ; Andersen, OM; Willnow, TE; GraffRadford, N; Petersen, RC; Dickson, D; Der, SD; Fraser, PE; SchmittUlms, G; Younkin, S; Mayeux, R; Farrer, LA; St GeorgeHyslop, P2007200
 
The sortilin-related receptor SORL1 is genetically associated with Alzheimer’s Disease
Journal:
Nature Genetics
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.genetics.nature.com
Rogaeva, E; Meng, Y; Lee, JH; Gu, Y; Kawarai, T; Zou, F; Katayama, T; Baldwin, CT; Cheng, R; Hasegawa, H; Chen, F; Shibata, N; Lunetta, KL; Song, Y; Fraser, PE; Schmitt-Ulms, G; Younkin, S; Mayeux, R; Farrer, LA; St George-Hyslop, P2007205
 
The sortilin-related recentor SORLA is functionally and genetically associated with Alzheimer Disease.
Proceedings/Conference:
The 55th american society of Human Genetics meeting. October25-29, 2005, Salt Lake City Utah
Meng, Y; Rogaeva, E; Lee, J.H; Gu, Y.J; Kawarai, T.; Katayama, T; Erlich, P; Baldwin, C.T; Cheng, R; Hasegawa, H; Chen, F; Shibata, N; Lunetta, K.L; Cupples, L.A; Song, Y; Fraser, P.E; Westaway, D; Mayeux, R; Farrer, L.A; St. George-Hyslop, P2005140
 
A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families
Journal:
Journal of the American Medical Association
Publisher:
American Medical Association. The Journal's web site is located at http://jama.ama-assn.org/index.dtl
Athan, ES; Williamson, J; Ciappa, A; Santana, V; Romas, SN; Lee, JH; Rondon, H; Lantigua, RA; Medrano, M; Torres, M; Arawaka, S; Rogaeva, E; Song, YQ; Sato, C; Kawarai, T; Fafel, KC; Boss, MA; Seltzer, WK; Stern, Y; St GeorgeHyslop, P; Tycko, B; Mayeux, R2001218
 
Screening for PS1 mutations in a referral-based series of AD cases: 21 Novel mutations
Journal:
Neurology
Publisher:
Lippincott Williams & Wilkins. The Journal's web site is located at http://www.neurology.org
Rogaeva, EA; Fafel, KC; Song, YQ; Medeiros, H; Sato, C; Liang, Y; Richard, E; Rogaev, EI; Frommelt, P; Sadovnick, AD; Meschino, W; Rockwood, K; Boss, MA; Mayeux, R; St GeorgeHyslop, P2001192
 
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease
Journal:
Archives of Neurology
Publisher:
American Medical Association. The Journal's web site is located at http://www.archneurol.com
Devi, G; Fotiou, A; Jyrinji, D; Tycko, B; DeArmand, S; Rogaeva, E; Song, YQ; Medieros, H; Liang, Y; Orlacchio, A; Williamson, J; St GeorgeHyslop, P; Mayeux, R2000199
 
Imaging physiologic dysfunction neurotechnique of individual hippocampal subregions in humans and genetically modified mice
Journal:
Neuron
Publisher:
Cell Press. The Journal's web site is located at http://www.elsevier.com/locate/neuron
Small, SA; Wu, EX; Bartsch, D; Perera, GM; Lacefield, CO; Delapaz, R; Mayeux, R; Stern, Y; Kandel, ER2000194
 
The APOE-ε4 allele and Alzheimer disease among African Americans, Hispanics, and whites [3] (multiple letters)
Journal:
Journal of the American Medical Association
Publisher:
American Medical Association. The Journal's web site is located at http://jama.ama-assn.org/index.dtl
Barker, W; Harwood, D; Duara, R; Mullan, M; Fallin, D; Hyslop, PSG; Rogaeva, E; Song, Y; Farkas, BL; Grant, WB; Mendez, HA; Tang, MX; Mayeux, R1998211
 
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