Научные интересы

Специалист в области молекулярной генетики, генетики человека и животных, медицинской генетики, нейрогенетики, эволюционной геномики, ДНК-криминалистики, исторической генетики. Основные научные интересы лежат в области изучения функций генов человека и животных с использованием методов геномного секвенирования и биоинформатики.

Научные публикации

Rogaev E.I., Sherrington R., Rogaeva E., Ikeda M., Levesque G., Liang Y., Chi H., Lin C., Holman K., Tsuda Т., Mar L., Sorbi S., Nacmias В., Piacentini S., Amaducci L., Chumakov I., Cohen D., Lannfelt L., Fraser P., Rommens J., St. George-Hyslop P. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature (London), 1995, V.376, 775-778.
Sherrington R. and ++Rogaev E.I. (sharing first co-authorship: contributed equally). Liang Y., Rogaeva Е.А., Levesque G., Ikeda M., Chi H., Lin C., Li G., Holman K., Tsuda Т., Mar L., Foncin J.F., Bruni A.C., Montesi М-Р., Sorbi S., Rainero I., Pinessi L., Nee L., Chumakov I., Pollen D., Brookes A,, Sanseau P., Pollinsky R.L., Wasco W., Da Silva H.A., Haines J.L., Pericak-Vance M.A., Tanzi R.E., Roses A., Frazer P., Rommens J., St. George-Hyslop P. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature (London), 1995, V.375, 754-760.
Grigorenko, A. P., Moliaka, Y. K., Soto, M. C., Mello C. C. and Rogaev, E. I. The Caenorhabditis elegans IMPAS gene, imp-2, is essential for development and is functionally distinct from related presenilins. Proc Natl Acad Sci U S A, 2004, v. 101, pp. 14955-14960.
Rogaev EI, Moliaka YK, Malyarchuk BA, Kondrashov FA, Derenko MV, Chumakov I, Grigorenko AP. Complete Mitochondrial Genome and Phylogeny of Pleistocene Mammoth Mammuthus primigenius. PLoS Biol. 2006; 4(3):e73.
Kazantseva A, Goltsov A, Zinchenko R, Grigorenko AP, Abrukova AV, Moliaka YK, Kirillov AG, Guo Z, Lyle S, Ginter EK, Rogaev EI. Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH. Science. 2006; 314(5801):982-5.
Rogaev E.I., Grigorenko A.P., Faskhutdinova G., Kittler E.L., Moliaka Y.K. Genotype Analysis Identifies the Cause of the "Royal Disease" // Science. 2009. V. 326, No. 5954. P.817-118.
Rogaev E.I., Grigorenko A.P., Moliaka Y.K., Faskhutdinova G., Goltsov A., Lahti A., Hildebrandt C., Kittler E.L., Morozova I. Genomic identification in the historical case of the Nicholas II royal family. // Proc Natl Acad Sci U S A. 2009. V. 106. No. 13. P. :5258-5263.
Moroz LL*, Kocot KM, Citarella MR, Dosung S, Norekian TP, Povolotskaya IS, Grigorenko AP, Dailey C, Berezikov E, Buckley KM, Ptitsyn A, Reshetov D, Mukherjee K, Moroz TP, Bobkova Y, Yu F, Kapitonov VV, Jurka J, Bobkov YV, Swore JJ, Girardo DO, Fodor A, Gusev F, Sanford R, Bruders R, Kittler E, Mills CE, Rast JP, Derelle R, Solovyev VV, Kondrashov FA, Swalla BJ, Sweedler JV, Rogaev EI* (*co-corresponding authors), Halanych KM, Kohn AB*. The ctenophore genome and the evolutionary origins of neural systems. Nature. 2014 Jun 5;510(7503):109-14. doi: 10.1038/nature13400.
Gusev FE, Reshetov DA, Mitchell AC, Andreeva TV, Dincer A, Grigorenko AP, Fedonin G, Halene T, Aliseychik M, Goltsov AY, Solovyev V, Brizgalov L, Filippova E, Weng Z, Akbarian S, Rogaev EI. Epigenetic-genetic chromatin footprinting identifies novel and subject-specific genes active in prefrontal cortex neurons. FASEB J. 2019 Apr 10:fj201802646R. doi: 10.1096/fj.201802646R
Sergey Nurk, Sergey Koren, Arang Rhie, Mikko Rautiainen, Andrey V. Bzikadze, AllaMikheenko, Mitchell R. Vollger, Nicolas Altemose, Lev Uralsky,..... Evgeny I. Rogaev et al. The complete sequence of a human genome. Science. 2022. In the press. doi: https://doi.org/10.1101/2021.05.26.445798

Премии и награды

Государственная премия Российской Федерации в области науки и техники за 1996 год.

Государственная премия Российской Федерации в области науки и технологий за 2017 год.

Персональные профили исследователя

Web of Science: AAN-7662-2020
Scopus: 35391858800
РИНЦ: 144919
ORCID: 0000-0003-0594-4767