| Title | Author(s) | Year | View Count |
 | Further analysis of the nicastrin: presenilin complex” | Chen, F; Yu, G; Arawaka, S; Nishimura, M; Kawarai, T; Yu, H; Tandon, A; Supala, A; Song, Y; Rogaeva, E; Milman, P; Sato, C; Lee, J; Song, L; Zhang, L; Fraser, PE; St George-Hyslop, P | 2006 | 221 |
 | PS1 Alzheimer's disease family with spastic paraplegia: The search for a gene modifier | Rogaeva, E; Bergeron, C; Sato, C; Moliaka, I; Kawarai, T; Toulina, A; Song, YQ; Kolesnikova, T; Orlacchio, A; Bernardi, G; St GeorgeHyslop, PH | 2003 | 70 |
| A Novel PS1 Case of Variant Alzheimer’s Disease with Spastic Paraplegia: The Search for a Gene-Modifier | Rogaeva, EA; Moliaka, I; Toshitaka, K; Sato, C; Medeiros, H; Song, Y; Liang, Y; Kolesnikova, T; Bergeron, C; St George-Hyslop, PH | 2002 | 97 |
| Chromosome 10 and 12 Loci for Late-Onset Alzheimer’s Disease: Genetic Linkage and Case-Control Association Studies | Rogaeva, EA; Erlich, P; Song, Y; Moliaka, I; Kawarai, T; Paterson, A; Sato, C; Medeiros, H; Liang, Y; Kolesnikova, T; Sorbi, S; Bruni, A; Farrer, LA; St George-Hyslop, PH | 2002 | 93 |
| Low frequency of TAU mutations and further genetic heterogeneity in FTD | Kawarai, T; Rogaeva, E; Song, Y; Moliaka, Y; Medeiros, H; Liang, Y; Sato, C; Ling, S; Fong, M; Kolesnikova, T; Bergeron, C; Lang, AE; Paterson, AD; Orlacchio, A; Bernardi, G; Rockwood, K; Allegri, R; Rainero, I; Pinessi, L; Cappa, G; Kertesz, A; Bruni, AC; Freedman, M; Ahern, GL; Tuite, P; Fornazzari, L; St George-Hyslop, P | 2002 | 93 |
| Screening for PS1 mutations in a referral-based series of AD cases: 21 Novel mutations | 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, P | 2001 | 83 |
| Nicastrin binds to membrane-tethered Notch | Chen, F; Yu, G; Arawaka, S; Nishimura, M; Kawarai, T; Yu, H; Tandon, A; Supala, A; Song, YQ; Rogaeva, E; Milman, P; Sato, C; Yu, C; Janus, C; Lee, J; Song, L; Zhang, L; Fraser, PE; St GeorgeHyslop, PH | 2001 | 113 |
| A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families | 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, R | 2001 | 107 |
| Association between angiotensin-converting enzyme and Alzheimer disease | Farrer, LA; Shcrbatich, T; Kcryanov, SA; Korovaitscva, GI; Rogaeva, EA; Petruk, S; Premkumar, S; Moliaha, Y; Song, YQ; Pei, Y; Sato, C; Selczncva, ND; Voshresenshaya, S; Golimbct, V; Sorbi, S; Duara, R; Gavrilova, S; St GeorgcHyslop, PH; Rogaev, EL | 2000 | 110 |
| Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and βAPP processing | Yu, G; Nishimura, M; Arawaka, S; Levitan, D; Zhang, L; Tandon, A; Song, YQ; Rogaeva, E; Chen, F; Kawarai, T; Supala, A; Levesque, L; Yu, H; Yang, DS; Holmes, E; Milman, P; Liang, Y; Zhang, DM; Xu, DH; Sato, C; Rogaev, E; Smith, M; Janus, C; Zhang, Y; Aebersold, R; Farrer, L; Sorbl, S; Bruni, A; Fraser, P; GeorgeHyslop, PS | 2000 | 120 |
| Mutation of the conserved N-terminal cysteine (Cys92) of human presenilin 1 causes increased Aβ42 secretion in mammalian cells but impaired Notch/lin-12 signalling in C. elegans | Dong Mei Zhang; Levitan, D; Yu, G; Nishimura, M; Chen, F; Tandon, A; Kawarai, T; Arawaka, S; Supala, A; Song, YQ; Rogaeva, E; Liang, Y; Holmes, E; Milman, P; Sato, C; Zhang, L; St GeorgeHyslop, P | 2000 | 102 |
|
