Ekaterina Rogaeva
Ekaterina Rogaeva
Verified email at utoronto.ca
Title
Cited by
Cited by
Year
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), 754-760, 1995
50261995
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
36532011
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), 1452-1458, 2013
31282013
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), 775-778, 1995
24671995
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
21292013
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), 436-441, 2011
17302011
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
16372009
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), 168-177, 2007
12082007
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), 48-54, 2000
12022000
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
10322002
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), 2018
10262018
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
8512019
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14
P St George-Hyslop, J Haines, EI Rogaev, M Mortilla, G Vaula, ...
Nature genetics 2 (4), 330-334, 1992
6141992
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
5492017
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), 550-554, 2014
4172014
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
4112010
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ...
Nature neuroscience 17 (5), 664-666, 2014
3922014
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
3842005
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
JD Rohrer, JM Nicholas, DM Cash, J van Swieten, E Dopper, L Jiskoot, ...
The Lancet Neurology 14 (3), 253-262, 2015
3732015
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), 1208-1212, 2006
3692006
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