Ekaterina Rogaeva
Ekaterina Rogaeva
Verified email at utoronto.ca
TitleCited byYear
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
R Sherrington, EI Rogaev, Y Liang, EA Rogaeva, G Levesque, M Ikeda, ...
Nature 375 (6534), 754, 1995
44751995
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron 72 (2), 257-268, 2011
28012011
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
EI Rogaev, R Sherrington, EA Rogaeva, G Levesque, M Ikeda, Y Liang, ...
Nature 376 (6543), 775, 1995
21941995
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452, 2013
19572013
TREM2 variants in Alzheimer's disease
R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ...
New England Journal of Medicine 368 (2), 117-127, 2013
15292013
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ...
Nature genetics 43 (5), 436, 2011
13902011
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
11852009
Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and βAPP processing
G Yu, M Nishimura, S Arawaka, D Levitan, L Zhang, A Tandon, YQ Song, ...
Nature 407 (6800), 48, 2000
11172000
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
E Rogaeva, Y Meng, JH Lee, Y Gu, T Kawarai, F Zou, T Katayama, ...
Nature genetics 39 (2), 168, 2007
10492007
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia
I Chumakov, M Blumenfeld, O Guerassimenko, L Cavarec, M Palicio, ...
Proceedings of the National Academy of Sciences 99 (21), 13675-13680, 2002
9752002
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14
PH St George-Hyslop, JL Haines, EI Rogaev, M Mortilla, G Vaula, ...
Nature genetics 2 (4), 330, 1992
5481992
Wild-type PINK1 prevents basal and induced neuronal apoptosis, a protective effect abrogated by Parkinson disease-related mutations
A Petit, T Kawarai, E Paitel, N Sanjo, M Maj, M Scheid, F Chen, Y Gu, ...
Journal of Biological Chemistry 280 (40), 34025-34032, 2005
3462005
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
G Jun, AC Naj, GW Beecham, LS Wang, J Buros, PJ Gallins, JD Buxbaum, ...
Archives of neurology 67 (12), 1473-1484, 2010
3452010
TMP21 is a presenilin complex component that modulates γ-secretase but not ɛ-secretase activity
F Chen, H Hasegawa, G Schmitt-Ulms, T Kawarai, C Bohm, T Katayama, ...
Nature 440 (7088), 1208, 2006
3342006
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ...
Nature 505 (7484), 550, 2014
3302014
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), eaap8757, 2018
3182018
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant
R Sherrington, S Froelich, S Sorbi, D Campion, H Chi, EA Rogaeva, ...
Human molecular genetics 5 (7), 985-988, 1996
3011996
Deciphering the role of heterozygous mutations in genes associated with parkinsonism
C Klein, K Lohmann-Hedrich, E Rogaeva, MG Schlossmacher, AE Lang
The Lancet Neurology 6 (7), 652-662, 2007
2762007
Microbleed topography, leukoaraiosis, and cognition in probable Alzheimer disease from the Sunnybrook dementia study
JA Pettersen, G Sathiyamoorthy, FQ Gao, G Szilagyi, NK Nadkarni, ...
Archives of neurology 65 (6), 790-795, 2008
2692008
Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation
S Hague, E Rogaeva, D Hernandez, C Gulick, A Singleton, M Hanson, ...
Annals of neurology 54 (2), 271-274, 2003
2692003
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Articles 1–20