Results 1 to 11 of 11
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TypeTitleAuthor(s)YearViews
A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expressionFarrell, JJ; Sherva, RM; Chen, ZY; Luo, HY; Chu, BF; Ha, SY; Li, CK; Lee, ACW; Li, RCH; Li, CK; Yuen, HL; So, JCC; Ma, ESK; Chan, LC; Chan, V; Sebastiani, P; Farrer, LA; Baldwin, CT; Steinberg, MH; Chui, DHK2011182
 
BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathiesSedgewick, AE; Timofeev, N; Sebastiani, P; So, JCC; Ma, ESK; Chan, LC; Fucharoen, G; Fucharoen, S; Barbosa, CG; Vardarajan, BN; Farrer, LA; Baldwin, CT; Steinberg, MH; Chui, DHK2008115
 
Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong KongGibney, GT; Panhuysen, CIM; So, JCC; Ma, ESK; Shau, YH; Chi, KL; Lee, ACW; Chi, KL; Hui, LY; Yu, LL; Johnson, DM; Farrell, JJ; Bisbee, AB; Farrer, LA; Steinberg, MH; Li, CC; Chui, DHK2008155
 
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer diseaseRogaeva, 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, P2007104
 
The sortilin-related receptor SORL1 is genetically associated with Alzheimer’s DiseaseRogaeva, 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, P2007146
 
Chromosome 10 and 12 Loci for Late-Onset Alzheimer’s Disease: Genetic Linkage and Case-Control Association StudiesRogaeva, 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, PH2002100
 
Mutations in the open reading frame of the β-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's diseaseNicolaou, 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, EA200195
 
Association between angiotensin-converting enzyme and Alzheimer diseaseFarrer, 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, EL2000108
 
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, RE1999102
 
Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneityRogaeva, 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, PH1998131
 
Association between bleomycin hydrolase and Alzheimer's disease in CaucasiansFarrer, LA; Abraham, CR; Haines, JL; Rogaeva, EA; Song, Y; McGraw, WT; Brindle, N; Premkumar, S; Scott, WK; Yamaoka, LH; Saunders, AM; Roses, AD; Auerbach, SA; Sorbi, S; Duara, R; PericakVance, MA; St GeorgeHyslop, PH1998135
 
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