| Title | Author(s) | Year | View Count |
 | The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease | 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, P | 2007 | 69 |
 | The sortilin-related receptor SORL1 is genetically associated with Alzheimer’s Disease | 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, P | 2007 | 113 |
| 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 | 222 |
| 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 |
| 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 | 94 |
| 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 |
| 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 | 114 |
| 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 | 108 |
| 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 | 62 |
| Mutation of conserved aspartates affect maturation of presenilin 1 and presenilin 2 complexes | Yu, G; Chen, F; Nishimura, M; Steiner, H; Tandon, A; Kawarai, T; Arawaka, S; Supala, A; Song, YQ; Rogaeva, E; Holmes, E; Zhang, DM; Milman, P; Fraser, P; Haass, C; St GeorgeHyslop, P | 2000 | 120 |
| Mutation of conserved aspartates affects maturation of both aspartate mutant and endogenous presenilin 1 and presenilin 2 complexes | Yu, G; Chen, F; Nishimura, M; Steiner, H; Tandon, A; Kawarai, T; Arawaka, S; Supala, A; Song, YQ; Rogaeva, E; Holmes, E; Zhang, DM; Milman, P; Fraser, PE; Haass, C; St GeorgeHyslop, P | 2000 | 134 |
| Carboxyl-terminal fragments of alzheimer β-amlyloid precursor protein accumulate in restricted and unpredicted intracellular compartments in presenilin 1-deficient cells | Chen, F; Yang, DS; Petanceska, S; Yang, A; Tandon, A; Yu, G; Rozmahel, R; Ghiso, J; Nishimura, M; Zhang, DM; Kawarai, T; Levesque, G; Mills, J; Levesque, L; Song, YQ; Rogaeva, E; Westaway, D; Mount, H; Gandy, S; St GeorgeHyslop, P; Fraser, PE | 2000 | 125 |
| 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 | 103 |
| 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 | 72 |
| Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity | Rogaeva, E; Premkumar, S; Song, Y; Sorbi, S; Brindle, N; Paterson, A; Duara, R; Levesque, G; Yu, G; Nishimura, M; Ikeda, M; O'Toole, C; Kawarai, T; Jorge, R; Vilarino, D; Bruni, AC; Farrer, LA; St GeorgeHyslop, PH | 1998 | 142 |
| 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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