| Title | Author(s) | Year | View Count |
 | 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 |
| Clinical and genetic study of a large Italian family linked to SPG12 locus | Orlacchio, A; Kawarai, T; Rogaeva, E; Song, Y; Paterson, AD; Bernardi, G; St George-Hyslop, PH | 2002 | 105 |
 | 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 |
| Mutations in the open reading frame of the β-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease | Nicolaou, M; Song, YQ; Sato, CA; Orlacchio, A; Kawarai, T; Medeiros, H; Liang, Y; Sorbi, S; Richard, E; Rogaev, EI; Moliaka, Y; Bruni, AC; Jorge, R; Percy, M; Duara, R; Farrer, LA; St GeorgeHyslop, P; Rogaeva, EA | 2001 | 61 |
| Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease | 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, R | 2000 | 102 |
| An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease [5] (multiple letters) | Rogaeva, EA; Premkumar, S; Grubber, J; Serneels, L; Scott, WK; Kawarai, T; Song, Y; Hill, DM; AbouDonia, SM; Martin, ER; Vance, JJ; Yu, G; Orlacchio, A; Pei, Y; Nishimura, M; Supala, A; Roberge, B; Saunders, AM; Roses, AD; Schmechel, D; CraneGatherum, A; Sorbi, S; Bruni, A; Small, GW; Conneally, PM; Haines, JL; Van Leuven, F; St GeorgeHyslop, PH; Farrer, LA; Pericak Vance, MA; Blacker, D; Crystal, AS; Wilcox, MA; Laird, NM; Tanzi, RE | 1999 | 71 |
| Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE | Song, YQ; Rogaeva, E; Premkumar, S; Brindle, N; Kawarai, T; Orlacchio, A; Yu, G; Levesque, G; Nishimura, M; Ikeda, M; Pei, Y; O'Toole, C; Duara, R; Barker, W; Sorbi, S; Freedman, M; Farrer, L; St GeorgeHyslop, P | 1998 | 109 |
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