| Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease REA Sherrington R, Rogaev EI, Liang Y Nature 375 (6534), 754-60, 1995 | 5527 | 1995 |
| 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 | 2706 | 1995 |
| The complete sequence of a human genome S Nurk, S Koren, A Rhie, M Rautiainen, AV Bzikadze, A Mikheenko, ... Science 376 (6588), 44-53, 2022 | 1814 | 2022 |
| 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 | 1287 | 2000 |
| 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 | 1096 | 2002 |
| The ctenophore genome and the evolutionary origins of neural systems LL Moroz, KM Kocot, MR Citarella, S Dosung, TP Norekian, ... Nature 510 (7503), 109-114, 2014 | 779 | 2014 |
| Telomere shortening is associated with cell division in vitro and in vivo RC Allsopp, E Chang, M Kashefi-Aazam, EI Rogaev, MA Piatyszek, ... Experimental cell research 220 (1), 194-200, 1995 | 733 | 1995 |
| 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 | 653 | 1992 |
| 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 | 439 | 1996 |
| Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a PA Underhill, NM Myres, S Rootsi, M Metspalu, LA Zhivotovsky, RJ King, ... European journal of human genetics 18 (4), 479-484, 2010 | 318 | 2010 |
| A set of differentially expressed miRNAs, including miR-30a-5p, act as post-transcriptional inhibitors of BDNF in prefrontal cortex N Mellios, HS Huang, A Grigorenko, E Rogaev, S Akbarian Human molecular genetics 17 (19), 3030-3042, 2008 | 317 | 2008 |
| Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant H Li, S Borinskaya, K Yoshimura, N Kal’Ina, A Marusin, VA Stepanov, ... Annals of human genetics 73 (3), 335-345, 2009 | 309 | 2009 |
| Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations EA Rogaeva, KC Fafel, YQ Song, H Medeiros, C Sato, Y Liang, E Richard, ... Neurology 57 (4), 621-625, 2001 | 265 | 2001 |
| Complete genomic and epigenetic maps of human centromeres N Altemose, GA Logsdon, AV Bzikadze, P Sidhwani, SA Langley, ... Science 376 (6588), eabl4178, 2022 | 257 | 2022 |
| Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH A Kazantseva, A Goltsov, R Zinchenko, AP Grigorenko, AV Abrukova, ... Science 314 (5801), 982-985, 2006 | 233 | 2006 |
| Role for glyoxalase I in Alzheimer's disease F Chen, MA Wollmer, F Hoerndli, G Münch, B Kuhla, EI Rogaev, M Tsolaki, ... Proceedings of the National Academy of Sciences 101 (20), 7687-7692, 2004 | 195 | 2004 |
| Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with … Y Takiyama, S Igasrashi, EA Rogaeva, K Endo, EI Rogaev, H Tanaka, ... Human molecular genetics 4 (7), 1137-1146, 1995 | 186 | 1995 |
| Complete mitochondrial genome and phylogeny of Pleistocene mammoth Mammuthus primigenius EI Rogaev, YK Moliaka, BA Malyarchuk, FA Kondrashov, MV Derenko, ... PLoS biology 4 (3), e73, 2006 | 180 | 2006 |
| Analysis of the 5′ Sequence, Genomic Structure, and Alternative Splicing of thepresenilin-1Gene (PSEN1) Associated with Early Onset Alzheimer Disease EI Rogaev, R Sherrington, C Wu, G Levesque, Y Liang, EA Rogaeva, ... Genomics 40 (3), 415-424, 1997 | 175 | 1997 |
| Genotype analysis identifies the cause of the “royal disease” EI Rogaev, AP Grigorenko, G Faskhutdinova, ELW Kittler, YK Moliaka Science 326 (5954), 817-817, 2009 | 172 | 2009 |
