Ponomareva, N. V., Andreeva, T. V., Protasova, M. S., Shagam, L. I., Malina, D. D., Goltsov, A. Y., … Rogaev, E. I. (2017). Quantitative EEG during Normal Aging: Association with the Alzheimer's Disease Genetic Risk Variant in PICALM Gene. Neurobiology of Aging, 51, 177.e1–177.e8. [Link]

Biragyn, A., Aliseychik, M., & Rogaev, E. (2017). Potential Importance of B Cells in Aging and Aging-Associated Neurodegenerative Diseases. Seminars in Immunopathology. [Link]

Moskalev, A., Anisimov, V., Aliper, A., Artemov, A., Asadullah, K., Belsky, D., … Rogaev, E. …, Zhavoronkov, A. (2017). A Review of the Biomedical Innovations for Healthy Longevity. Aging, 9(1), 7–25. [Link]

Gunbin, K. V., Ponomarenko, M. P., Suslov, V. V., Gusev, F., Fedonin, G. G., & Rogaev, E. I. (2017). Evolution of Brain Active Gene Promoters in Human Lineage Towards the Increased Plasticity of Gene Regulation. Molecular Neurobiology. [Link]

Andreeva, T. V., Lukiw, W. J., & Rogaev, E. I. (2017). Biological Basis for Amyloidogenesis in AlzheimerS Disease. Biochemistry (Moscow), 82(2), 122–139. [Link]


Ignatieva, E. V., Afonnikov, D. A., Saik, O. V., Rogaev, E. I., & Kolchanov, N. A. (2016). A Compendium of Human Genes Regulating Feeding Behavior and Body Weight, Its Functional Characterization and Identification of GWAS Genes Involved in Brain-Specific PPI Network. BMC Genetics, 17(Suppl 3), 158. [Link]

Morozova, I., Flegontov, P., Mikheyev, A. S., Bruskin, S., Asgharian, H., Ponomarenko, P., …, Rogaev, E., …, Tatarinova, T. V. (2016). Toward High-Resolution Population Genomics Using Archaeological Samples. DNA Research: an International Journal for Rapid Publication of Reports on Genes and Genomes, 23(4), 295–310. [Link]

Andreeva, T. V., Tyazhelova, T. V., Rykalina, V. N., Gusev, F. E., Goltsov, A. Y., Zolotareva, O. I., … Rogaev, E. I. (2016). Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies. Sci Rep, 6, 26440. [Link]

Bhattacharjee, S., Zhao, Y., Dua, P., Rogaev, E. I., & Lukiw, W. J. (2016). microRNA-34a-Mediated Down-Regulation of the Microglial-Enriched Triggering Receptor and Phagocytosis-Sensor TREM2 in Age-Related Macular Degeneration. PLoS One, 11(3), e0150211. [Link]

Gunbin, K. V., Afonnikov, D. A., Kolchanov, N. A., Derevianko, A. P., & Rogaev, E. I. (2015). The evolution of Homo sapiens denisova and Homo sapiens neanderthalensis miRNA targeting genes in the prenatal and postnatal brain. BMC Genomics, 16 Suppl 13, S4. [Link]

Lisenkova, A. A., Grigorenko, A. P., Tyazhelova, T. V., Andreeva, T. V., Gusev, F. E., Manakhov, A. D., … Rogaev, E. I. (2016). Complete Mitochondrial Genome and Evolutionary Analysis of Turritopsis Dohrnii, The "immortal" jellyfish with a Reversible Life-Cycle. Molecular Phylogenetics and Evolution, 107, 232–238. [Link]

Morozova, I., Flegontov, P., Mikheyev, A. S., Bruskin, S., Asgharian, H., Ponomarenko, P., … Tatarinova, T. V. (2016). Toward High-Resolution Population Genomics Using Archaeological Samples. DNA Research: an International Journal for Rapid Publication of Reports on Genes and Genomes, 23(4), 295–310. [Link]

Protasova, M. S., Grigorenko, A. P., Tyazhelova, T. V., Andreeva, T. V., Reshetov, D. A., Gusev, F. E., … Rogaev, E. I. (2016). Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry. Eur J Hum Genet, 24(4), 550–555. [Link]

Ziccardi, W., Zhao, C., Shepelev, V., Uralsky, L., Alexandrov, I., Andreeva, T., … Doering, J. (2016). Clusters of Alpha Satellite on Human Chromosome 21 Are Dispersed Far onto the Short Arm and Lack Ancient Layers. Chromosome Research: An International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology, 24(3), 421–436. [Link]

2011 - 2015

Shepelev, V. A., Uralsky, L. I., Alexandrov, A. A., Yurov, Y. B., Rogaev, E. I., & Alexandrov, I. A. (2015). Annotation of suprachromosomal families reveals uncommon types of alpha satellite organization in pericentromeric regions of hg38 human genome assembly. Genom Data, 5, 139–146. [Link]

Nizamutdinov, I. I., Andreeva, T. V., Stepanov, V. A., Marusin, A. V., Rogaev, E. I., Zasedatelev, A. S., & Nasedkina, T. V. (2013 Nov-Dec). [Biochip for determination of genetic markers of sporadic Alzheimer's disease in the Russian Slavic population]. Mol Biol (Mosk), 47(6), 949–958.

Bai, G., Cheung, I., Shulha, H. P., Coelho, J. E., Li, P., Dong, X., … Chen, J.-F. (2015). Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains. Hum Mol Genet, 24(5), 1441–1456. [Link]

Rykalina, V. N., Shadrin, A. A., Amstislavskiy, V. S., Rogaev, E. I., Lehrach, H., & Borodina, T. A. (2014). Exome sequencing from nanogram amounts of starting DNA: comparing three approaches. PLoS One, 9(7), e101154. [Link]

Moroz, L. L., Kocot, K. M., Citarella, M. R., Dosung, S., Norekian, T. P., Povolotskaya, I. S., … Kohn, A. B. (2014). The ctenophore genome and the evolutionary origins of neural systems. Nature, 510(7503), 109–114. [Link]

Ponomareva, N., Andreeva, T., Protasova, M., Shagam, L., Malina, D., Goltsov, A., … Rogaev, E. (2013). Age-dependent effect of Alzheimer's risk variant of CLU on EEG alpha rhythm in non-demented adults. Front Aging Neurosci, 5, 86. [Link]

Lukiw, W. J., Andreeva, T. V., Grigorenko, A. P., & Rogaev, E. I. (2012). Studying micro RNA Function and Dysfunction in Alzheimer's Disease. Front Genet, 3, 327. [Link]

Selezneva, N. D., Roshchina, I. F., Gavrilova, S. I., Fedorova, I. B., Gantman, M. V., Korovaitseva, G. I., … Rogaev, E. I. (2012). [Mental disorders of cognitive and non-cognitive spectrum in the first-degree relatives of patients with Alzheimer's disease]. Zh Nevrol Psikhiatr Im S S Korsakova, 112(10), 8–13.

Shulha, H. P., Crisci, J. L., Reshetov, D., Tushir, J. S., Cheung, I., Bharadwaj, R., … Akbarian, S. (2012). Human-specific histone methylation signatures at transcription start sites in prefrontal neurons. PLoS Biol, 10(11), e1001427. [Link]

Houston, I., Peter, C. J., Mitchell, A., Straubhaar, J., Rogaev, E., & Akbarian, S. (2013). Epigenetics in the human brain. Neuropsychopharmacology, 38(1), 183–197. [Link]

Rogaev, E. I. (2012). Genomics of behavioral diseases. Front Genet, 3, 45. [Link]

Ponomareva, N. V., Goltsov, A. Y., Kunijeva, S. S., Scheglova, N. S., Malina, D. D., Mitrofanov, A. A., … Rogaev, E. I. (2012). Age- and genotype-related neurophysiologic reactivity to oxidative stress in healthy adults. Neurobiol Aging, 33(4), 839.e11–21. [Link]

Berdichevets, I. N., Tyazhelova, T. V., Shimshilashvili, K. R., & Rogaev, E. I. (2010). Lysophosphatidic acid is a lipid mediator with wide range of biological activities. Biosynthetic pathways and mechanism of action. Biochemistry (Mosc), 75(9), 1088–1097.

Golenkina, S. A., Gol'tsov, A. I., Kuznetsova, I. L., Grigorenko, A. P., Andreeva, T. V., Reshetov, D. A., … Rogaev, E. I. (2010 Jul-Aug). [Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer's disease patients and in normal cohorts from Russian populations]. Mol Biol (Mosk), 44(4), 620–626.

Mellios, N., Galdzicka, M., Ginns, E., Baker, S. P., Rogaev, E., Xu, J., & Akbarian, S. (2012). Gender-specific reduction of estrogen-sensitive small RNA, miR-30b, in subjects with schizophrenia. Schizophr Bull, 38(3), 433–443. [Link]

... - 2010

Underhill, P. A., Myres, N. M., Rootsi, S., Metspalu, M., Zhivotovsky, L. A., King, R. J., … Kivisild, T. (2010). Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a. Eur J Hum Genet, 18(4), 479–484. [Link]

Rogaev, E. I., Grigorenko, A. P., Faskhutdinova, G., Kittler, E. L. W., & Moliaka, Y. K. (2009). Genotype analysis identifies the cause of the "royal disease". Science, 326(5954), 817. [Link]

Jarve, M., Zhivotovsky, L. A., Rootsi, S., Help, H., Rogaev, E. I., Khusnutdinova, E. K., … Sanchez, J. J. (2009). Decreased rate of evolution in Y chromosome STR loci of increased size of the repeat unit. PLoS One, 4(9), e7276. [Link]

Grigorenko, A. P., Borinskaya, S. A., Yankovsky, N. K., & Rogaev, E. I. (2009). Achievements and peculiarities in studies of ancient DNA and DNA from complicated forensic specimens. Acta Naturae, 1(3), 58–69.

Li, H., Borinskaya, S., Yoshimura, K., Kal'ina, N., Marusin, A., Stepanov, V. A., … Kidd, K. K. (2009). Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant. Ann Hum Genet, 73(Pt 3), 335–345. [Link]

Rogaev, E. I., Grigorenko, A. P., Moliaka, Y. K., Faskhutdinova, G., Goltsov, A., Lahti, A., … Morozova, I. (2009). Genomic identification in the historical case of the Nicholas II royal family. Proc Natl Acad Sci U S A, 106(13), 5258–5263. [Link]

Borinskaya, S., Kal'ina, N., Marusin, A., Faskhutdinova, G., Morozova, I., Kutuev, I., … Rogaev, E. (2009). Distribution of the alcohol dehydrogenase ADH1B*47His allele in Eurasia. Am J Hum Genet, 84(1), 89–92; author reply 92–94. [Link]

Rogaev, E. I., Borinskaia, S. A., Islamgulov, D. V., & Grigorenko, A. P. (2008 Sep-Oct). [Human microRNA in norm and pathology]. Mol Biol (Mosk), 42(5), 751–764.

Mellios, N., Huang, H.-S., Grigorenko, A., Rogaev, E., & Akbarian, S. (2008). A set of differentially expressed miRNAs, including miR-30a-5p, act as post-transcriptional inhibitors of BDNF in prefrontal cortex. Hum Mol Genet, 17(19), 3030–3042. [Link]

Borinskaia, S. A., Kal'ina, N. R., Sanina, E. D., Kozhekbaeva, Z. M., Gupalo, E. I., Garmash, I. V., … Iankovskii, N. K. (2007). [Polymorphism of the apolipoprotein E gene (APOE) in the populations of Russia and neighboring countries]. Genetika, 43(10), 1434–1440.

Burmistrova, O. A., Goltsov, A. Y., Abramova, L. I., Kaleda, V. G., Orlova, V. A., & Rogaev, E. I. (2007). MicroRNA in schizophrenia: genetic and expression analysis of miR-130b (22q11). Biochemistry (Mosc), 72(5), 578–582.

Plotnikova, O. V., Kondrashov, F. A., Vlasov, P. K., Grigorenko, A. P., Ginter, E. K., & Rogaev, E. I. (2007). Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state. Am J Hum Genet, 81(1), 32–43. [Link]

Grigorenko, A. P., & Rogaev, E. I. (2007 Mar-Apr). [Molecular basics of Alzheimer's disease]. Mol Biol (Mosk), 41(2), 331–345.

Ponomareva, N. V., Korovaitseva, G. I., & Rogaev, E. I. (2008). EEG alterations in non-demented individuals related to apolipoprotein E genotype and to risk of Alzheimer disease. Neurobiol Aging, 29(6), 819–827. [Link]

Kazantseva, A., Goltsov, A., Zinchenko, R., Grigorenko, A. P., Abrukova, A. V., Moliaka, Y. K., … Rogaev, E. I. (2006). Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH. Science, 314(5801), 982–985. [Link]

Papassotiropoulos, A., Lambert, J.-C., {Wavrant-De Vrieze}, F., Wollmer, M. A., {von der Kammer}, H., Streffer, J. R., … Nitsch, R. M. (2005). Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease. Neurodegener Dis, 2(5), 233–241. [Link]

Rogaev, E. I., Moliaka, Y. K., Malyarchuk, B. A., Kondrashov, F. A., Derenko, M. V., Chumakov, I., & Grigorenko, A. P. (2006). Complete mitochondrial genome and phylogeny of Pleistocene mammoth Mammuthus primigenius. PLoS Biol, 4(3), e73. [Link]

Goltsov, A. Y., Loseva, J. G., Andreeva, T. V., Grigorenko, A. P., Abramova, L. I., Kaleda, V. G., … Rogaev, E. I. (2006). Polymorphism in the 5'-promoter region of serine racemase gene in schizophrenia. Mol Psychiatry, 11(4), 325–326. [Link]

Rogaev, E. I. (2005). Small RNAs in human brain development and disorders. Biochemistry (Mosc), 70(12), 1404–1407.

Golimbet, V. E., Lebedeva, I. S., Gritsenko, I. K., Korovaitseva, G. I., Alfimova, M. V., Lezheiko, T. V., … Rogaev, E. I. (2005). [A study of some genes related to serotoninergic and dopaminergic systems and auditory evoked-potentials (P300) in patients with schizophrenia and spectrum disorders and their first-degree relatives]. Zh Nevrol Psikhiatr Im S S Korsakova, 105(10), 35–41.

Rogaev, E. (2004). Academic psychiatry in Russia: new times, new challenges. Mol Psychiatry, 9(11), 975–976. [Link]

Grigorenko, A. P., Moliaka, Y. K., Soto, M. C., Mello, C. C., & Rogaev, E. I. (2004). 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, 101(41), 14955–14960. [Link]

Chen, F., Wollmer, M. A., Hoerndli, F., Munch, G., Kuhla, B., Rogaev, E. I., … Gotz, J. (2004). Role for glyoxalase I in Alzheimer's disease. Proc Natl Acad Sci U S A, 101(20), 7687–7692. [Link]

Golimbet, V. E., Alfimova, M. V., Shchebatykh, T. V., Abramova, L. I., Kaleda, V. G., & Rogaev, E. I. (2004). Serotonin transporter polymorphism and depressive-related symptoms in schizophrenia. Am J Med Genet B Neuropsychiatr Genet, 126B(1), 1–7. [Link]

Moliaka, Y. K., Grigorenko, A., Madera, D., & Rogaev, E. I. (2004). Impas 1 possesses endoproteolytic activity against multipass membrane protein substrate cleaving the presenilin 1 holoprotein. FEBS Lett, 557(1-3), 185–192.

Bobrysheva, I. V., Grigorenko, A. P., Novosadova, E. V., Kal'ina, N. R., Arsenyeva, E. L., Grivennikov, I. A., … Rogaev, E. I. (2003). Effects of human presenilin 1 isoforms on proliferation and survival of rat pheochromocytoma cell line PC12. Biochemistry (Mosc), 68(6), 611–617.

Golimbet, V. E., Alfimova, M. V., Shcherbatykh, T. V., & Rogaev, E. I. (2003). [Gene insertion and deletion polymorphism in the serotonin transporter gene and personality traits measured by MMPI]. Genetika, 39(4), 534–539.

Golimbet, V. E., Alfimova, M. V., Shcherbatikh, T., Kaleda, V. G., Abramova, L. I., & Rogaev, E. I. (2003). Serotonin transporter gene polymorphism and schizoid personality traits in the patients with psychosis and psychiatrically well subjects. World J Biol Psychiatry, 4(1), 25–29.

Chumakov, I., Blumenfeld, M., Guerassimenko, O., Cavarec, L., Palicio, M., Abderrahim, H., … Cohen, D. (2002). Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc Natl Acad Sci U S A, 99(21), 13675–13680. [Link]

Riazanskaia, N., Lukiw, W. J., Grigorenko, A., Korovaitseva, G., Dvoryanchikov, G., Moliaka, Y., … Rogaev, E. (2002). Regulatory region variability in the human presenilin-2 (PSEN2) gene: potential contribution to the gene activity and risk for AD. Mol Psychiatry, 7(8), 891–898. [Link]

Grigorenko, A. P., Moliaka, Y. K., Korovaitseva, G. I., & Rogaev, E. I. (2002). Novel class of polytopic proteins with domains associated with putative protease activity. Biochemistry (Mosc), 67(7), 826–835.

Golimbet, V. E., Alfimova, M. V., Shcherbatykh, T. V., & Rogaev, E. I. (2002). [Allele polymorphism of the serotonin transporter gene and clinical heterogeneity of depressive disorders]. Genetika, 38(5), 671–677.

Pankov, I. A., Iatsyshina, S. B., Karpova, S. K., Chekhranova, M. K., Popova, I. P., Grigorian, O. N., & Rogaev, E. I. (2002 Jan-Feb). [Screening of mutations in genes of pro-opiomelanocortin in patients with constitutional exogenous obesity]. Vopr Med Khim, 48(1), 121–130.

Maliarchuk, B. A., Derenko, M. V., Denisova, G. A., Nassiri, M. R., & Rogaev, E. I. (2002). [Mitochondrial DNA polymorphism in populations of the Caspian region and southeastern Europe]. Genetika, 38(4), 534–538.

Iatsyshina, S. B., Moliaka, I. K., Karpova, S. K., Chekhranova, M. K., Popova, I. P., Grigorian, O. N., … Rogaev, E. I. (2002). [Study of the association between constitutional exogenous obesity and polymorphism of the apolipoprotein B gene]. Genetika, 38(2), 285–288.

Maliarchuk, B. A., Denisova, G. A., Derenko, M. V., Rogaev, E. I., Vlasenko, L. V., & Zhukova, S. G. (2001). [Variability in mitochondrial DNA in Russian inhabitants from Krasnodar Krai, Belgorod and the lower Novgorod region]. Genetika, 37(10), 1411–1416.

Nicolaou, M., Song, Y. Q., Sato, C. A., Orlacchio, A., Kawarai, T., Medeiros, H., … Rogaeva, E. A. (2001). Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease. Neurogenetics, 3(4), 203–206.

Golimbet, V. E., Shcherbatykh, T. V., Abramova, L. I., Kaleda, V. G., Oleichik, I. V., Orlova, V. A., & Rogaev, E. I. (2001). [Serotonin transporter gene polymorphism in families with schizophrenia]. Zh Nevrol Psikhiatr Im S S Korsakova, 101(10), 40–41.

Ginter, E. K., Kirillov, A. G., & Rogaev, E. I. (2001). [Autosomal-dominant osteopetrosis in Chuvashiya]. Genetika, 37(8), 1152–1155.

Rogaeva, E. A., Fafel, K. C., Song, Y. Q., Medeiros, H., Sato, C., Liang, Y., … {St George-Hyslop}, P. (2001). Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations. Neurology, 57(4), 621–625.

Golimbet, V. E., Mitiushina, N. G., Shcherbatykh, T. V., Aksenova, M. G., Abramova, L. I., Kaleda, V. G., … Rogaev, E. I. (2001). [Molecular genetic polymorphism of the genes of neurotransmitter systems in schizophrenics with early manifestation of the disease]. Zh Nevrol Psikhiatr Im S S Korsakova, 101(4), 48–50.

Golimbet, V. E., Alfimova, V. M., Shcherbatykh, T. V., Abramova, L. I., Kaleda, V. G., & Rogaev, E. I. (2001 May-Jun). [Insertion-deletion polymorphism of the serotonin carrier gene and evaluation of neurotism as a temperament trait in patients with affective disorders and mentally healthy people]. Mol Biol (Mosk), 35(3), 397–400.

Korovaitseva, G. I., Shcherbatykh, T. V., Selezneva, N. V., Gavrilova, S. I., Golimbet, V. E., Voskresenskaia, N. I., & Rogaev, E. I. (2001). [Genetic association between the apolipoprotein E (ApoE) gene alleles and various forms of Alzheimer's disease]. Genetika, 37(4), 529–535.

Shcherbatykh, T. V., Kiryanov, S. A., Korovaitseva, G. I., Selezneva, N. D., Voskresenskaya, N. I., Golimbet, V. E., … Rogaev, E. I. (2001 Mar-Apr). The angiotensin-converting enzyme gene as a possible risk or protective factor in Alzheimer's disease. Neurosci Behav Physiol, 31(2), 179–181.

Lukiw, W. J., Gordon, W. C., Rogaev, E. I., Thompson, H., & Bazan, N. G. (2001). Presenilin-2 (PS2) expression up-regulation in a model of retinopathy of prematurity and pathoangiogenesis. Neuroreport, 12(1), 53–57.

Yu, G., Nishimura, M., Arawaka, S., Levitan, D., Zhang, L., Tandon, A., … {St George-Hyslop}, P. (2000). Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and betaAPP processing. Nature, 407(6800), 48–54. [Link]

Farrer, L. A., Sherbatich, T., Keryanov, S. A., Korovaitseva, G. I., Rogaeva, E. A., Petruk, S., … Rogaev, E. I. (2000). Association between angiotensin-converting enzyme and Alzheimer disease. Arch Neurol, 57(2), 210–214.

Rogaev, E. I. (1999). [Genetic factors and a polygenic model of Alzheimer's disease]. Genetika, 35(11), 1558–1571.

Shcherbatykh, T. V., Kir'ianov, S. A., Korovaitsev, G. I., Selezneva, N. D., Voskresenskaia, N. I., Golimbet, V. E., … Rogaev, E. I. (1999). [Angiotensin-converting enzyme gene as a possible risk factor or protective factor in Alzheimer's disease]. Zh Nevrol Psikhiatr Im S S Korsakova, 99(9), 51–52.

Rogaev, E. I., Zinchenko, R. A., Dvoryachikov, G., Sherbatich, T., & Ginter, E. K. (1999). Total hypotrichosis: genetic form of alopecia not linked to hairless gene. Lancet, 354(9184), 1097–1098.

Korovaitseva, G. I., Premkumar, S., Grigorenko, A., Molyaka, Y., Galimbet, V., Selezneva, N., … Rogaev, E. I. (1999). Alpha-2 macroglobulin gene in early- and late-onset Alzheimer disease. Neurosci Lett, 271(2), 129–131.

Solov'ev, I. V., Iurov, I. B., Vorsanova, S. G., Marcais, B., Rogaev, E. I., Kapanadze, B. I., … Roizes, G. (1998). [Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization]. Genetika, 34(11), 1470–1479.

Rogaev, E. I. (1999). [Genetic basis for Alzheimer's disease and other dementias and prospects of molecular diagnosis]. Vestn Ross Akad Med Nauk, (1), 33–39.

Moliaka, I. K., Petruk, S. V., Kir'ianov, S. A., Dzhibladze, A. N., Chechetkin, A. O., Shcherbatykh, T. V., & Rogaev, E. N. (1998). [Association analysis of polymorphism in angiotensin-converting enzyme gene in ischemic stroke]. Zh Nevrol Psikhiatr Im S S Korsakova, 98(6), 35–37.

Rogaev, E. I. (1998 Jan-Feb). [Presenilins: detection and characterization of Alzheimer's disease genes]. Mol Biol (Mosk), 32(1), 71–83.

Korovaitseva, G. I., Bukina, A., Farrer, L. A., & Rogaev, E. I. (1997). Presenilin polymorphisms in Alzheimer's disease. Lancet, 350(9082), 959. [Link]

Kir'ianov, S. A., & Rogaev, E. I. (1997). [Rapid isolation of CpG-islands by PCR-amplification of genomic DNA fragments using a "CpG-enriched" primer]. Genetika, 33(7), 891–898.

Moliaka, I. K., Ovchinnikov, I. V., Shlenskii, A. B., Korovaitseva, G. I., & Rogaev, E. I. (1997). [DNA genotyposcoy in determining paternity: use of hybridized probes]. Genetika, 33(6), 831–835.

Rogaev, E. I., Sherrington, R., Wu, C., Levesque, G., Liang, Y., Rogaeva, E. A., … {St George-Hyslop}, P. (1997). Analysis of the 5' sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease. Genomics, 40(3), 415–424. [Link]

Boulianne, G. L., Livne-Bar, I., Humphreys, J. M., Liang, Y., Lin, C., Rogaev, E., & {St George-Hyslop}, P. (1997). Cloning and characterization of the Drosophila presenilin homologue. Neuroreport, 8(4), 1025–1029.

Rogaev, E. I., Ovchinnikov, I. V., Dzhorzh-Khislop, P., & Rogaeva, E. A. (1996). [Comparison of mitochondrial DNA sequences of T.N. Kulikovskii-Romanov, the nephew of Tsar Nikolai II Romanov, with DNA from the putative remains of the Tsar]. Genetika, 32(12), 1690–1692.

Sherrington, R., Froelich, S., Sorbi, S., Campion, D., Chi, H., Rogaeva, E. A., … {St George-Hyslop}, P. H. (1996). Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. Hum Mol Genet, 5(7), 985–988.

Igarashi, S., Takiyama, Y., Cancel, G., Rogaeva, E. A., Sasaki, H., Wakisaka, A., … Tsuji, S. (1996). Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat. Hum Mol Genet, 5(7), 923–932.

Rogaev, E. I., Rogaeva, E. A., Korovaitseva, G. I., Farrer, L. A., Petrin, A. N., Keryanov, S. A., … Ginter, E. K. (1996). Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35. Hum Mol Genet, 5(5), 699–703.

Trower, M. K., Orton, S. M., Purvis, I. J., Sanseau, P., Riley, J., Christodoulou, C., … Dykes, C. W. (1996). Conservation of synteny between the genome of the pufferfish (Fugu rubripes) and the region on human chromosome 14 (14q24.3) associated with familial Alzheimer disease (AD3 locus). Proc Natl Acad Sci U S A, 93(4), 1366–1369.

Golimbet, V. E., Ovchinnikov, I. V., Voskresenskaia, N. I., Iurov, I. B., Rogaev, E. I., Doronina, O. A., & Maksunova, I. V. (1996). [The search for a mutation in the gene coding the beta-amyloid protein precursor gene in patients with Alzheimer-type dementias]. Zh Nevrol Psikhiatr Im S S Korsakova, 96(1), 75–78.

Tsuda, T., Chi, H., Liang, Y., Rogaeva, E. A., Sherrington, R., Levesque, G., … Freedman, M. (1995). Failure to detect missense mutations in the S182 gene in a series of late-onset Alzheimer's disease cases. Neurosci Lett, 201(2), 188–190.

Allsopp, R. C., Chang, E., Kashefi-Aazam, M., Rogaev, E. I., Piatyszek, M. A., Shay, J. W., & Harley, C. B. (1995). Telomere shortening is associated with cell division in vitro and in vivo. Exp Cell Res, 220(1), 194–200. [Link]

Rogaev, E. I., Sherrington, R., Rogaeva, E. A., Levesque, G., Ikeda, M., Liang, Y., … Tsuda, T. (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. Nature, 376(6543), 775–778. [Link]

Sorbi, S., Nacmias, B., Forleo, P., Piacentini, S., Sherrington, R., Rogaev, E., … Amaducci, L. (1995). Missense mutation of S182 gene in Italian families with early-onset Alzheimer's disease. Lancet, 346(8972), 439–440.

Takiyama, Y., Igarashi, S., Rogaeva, E. A., Endo, K., Rogaev, E. I., Tanaka, H., … Saito, M. (1995). 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 Machado-Joseph disease. Hum Mol Genet, 4(7), 1137–1146.

Sherrington, R., Rogaev, E. I., Liang, Y., Rogaeva, E. A., Levesque, G., Ikeda, M., … {St George-Hyslop}, P. H. (1995). Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature, 375(6534), 754–760. [Link]

Rogaev, E. I., Rogaeva, E. A., & Dzhordzh-Khislop, P. (1995). [Direct detection of loci with pathologic trinucleotide repeats in diseases with anticipation]. Genetika, 31(4), 578–582.

Rogaev, E. I., Lukiw, W. J., Lavrushina, O., Rogaeva, E. A., & {St George-Hyslop}, P. H. (1994). The upstream promoter of the beta-amyloid precursor protein gene (APP) shows differential patterns of methylation in human brain. Genomics, 22(2), 340–347. [Link]

Tsuda, T., Lopez, R., Rogaeva, E. A., Freedman, M., Rogaev, E., Drachman, D., … McLachlan, D. R. (1994). Are the associations between Alzheimer's disease and polymorphisms in the apolipoprotein E and the apolipoprotein CII genes due to linkage disequilibrium? Ann Neurol, 36(1), 97–100. [Link]

{St George-Hyslop}, P., Rogaeva, E., Huterer, J., Tsuda, T., Santos, J., Haines, J. L., … McLachlan, D. R. (1994). Machado-Joseph disease in pedigrees of Azorean descent is linked to chromosome 14. Am J Hum Genet, 55(1), 120–125.

Lukiw, W. J., Rogaev, E. I., Wong, L., Vaula, G., McLachlan, D. R., & {St George Hyslop}, P. (1994). Protein-DNA interactions in the promoter region of the amyloid precursor protein (APP) gene in human neocortex. Brain Res Mol Brain Res, 22(1-4), 121–131.

Rogaev, E. I., Rogaeva, E. A., Ginter, E. K., Korovaitseva, G. I., Farrer, L., Shlenskii, A. B., … Mordovtsev, V. N. (1994). [Mapping the gene for palmoplantar hyperkeratosis (thylosis) to chromosome 17 in the 17q12-q24 region]. Genetika, 30(3), 326–329.

{St George-Hyslop}, P., McLachlan, D. C., Tsuda, T., Rogaev, E., Karlinsky, H., Lippa, C. F., & Pollen, D. (1994). Alzheimer's disease and possible gene interaction. Science, 263(5146), 537.

Iakimov, M. M., Rogozhin, I. S., Kal'deron, E., Matveeva, L. N., Karavaitseva, G. I., Bezborodov, A. M., & Rogaev, E. I. (1994 Jan-Feb). [Tn5-mutagenesis of the styrene-degrading strain Pseudomonas sp. Y2. Analysis of transformation products and DNA-scopy of the mutants obtained]. Prikl Biokhim Mikrobiol, 30(1), 55–63.

Rogaev, E. I., Lukiw, W. J., Vaula, G., Haines, J. L., Rogaeva, E. A., Tsuda, T., … {St George-Hyslop}, P. H. (1993). Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease. Neurology, 43(11), 2275–2279.

Rogaev, E. I., Rogaeva, E. A., Ginter, E. K., Korovaitseva, G. I., Farrer, L. A., Shlensky, A. B., … {St George-Hyslop}, P. H. (1993). Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes. Nat Genet, 5(2), 158–162. [Link]

Rogaev, E. I., Korovaitseva, G. I., Ginter, E. K., Prytkov, A. N., & Maksudova, K. A. (1993). [Mapping of the dominant gene of hyperkeratosis palmaris et plantaris in man]. Genetika, 29(7), 1180–1185.

Tupler, R., Rogaeva, E., Vaula, G., Mortilla, M., Lukiw, W., Liang, Y., … {St George-Hyslop}, P. (1993). A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) gene. Hum Mol Genet, 2(5), 620.

Bochkov, N. P., Rogaev, E. I., Moliaka, I. K., Shlenskii, A. B., & Asanov, A. I. (1993). [Detection of gamete mutations in the hypervariable region of human DNA for genetic monitoring]. Dokl Akad Nauk, 329(6), 785–786.

Ginter, E. K., Rogaev, E. I., Korovaitseva, G. I., Turaeva, S. M., Petrin, A. N., Spitsyn, V. A., & Tarlycheva, L. V. (1993). [Further analysis of location of the gene for inborn dominant Nochurli cataract]. Genetika, 29(4), 670–674.

{St George-Hyslop}, P., Haines, J., Rogaev, E., Mortilla, M., Vaula, G., Pericak-Vance, M., … {Crapper McLachlan}, D. (1992). Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nat Genet, 2(4), 330–334. [Link]

Rogaev, E., Rogaeva, E., Lukiw, W. J., Vaula, G., Liang, Y., Hancock, R., … {St George-Hyslop}, P. H. (1992). An informative microsatellite repeat polymorphism in the human neurofilament light polypeptide (NEFL) gene. Hum Mol Genet, 1(9), 781.

Rogaev, E. I., & Keryanov, S. A. (1992). Unusual variability of the complex dinucleotide repeat block at the SPN locus. Hum Mol Genet, 1(8), 657.

Rogaev, E. I., Keryanov, S. A., & Malyako, Y. K. (1992). Dinucleotide repeat polymorphisms at the P1, HBE1 and MYH7 loci. Hum Mol Genet, 1(4), 285.

Rogaev, E. I., Syrokvasheva, E. I., Pimenov, M. G., & Stegnova, T. V. (1992 Jan-Mar). [Human genotyposcopy: the identification of the species, sex and individual by DNA genetic imprints in a case connected with a murder attempt]. Sud Med Ekspert, 35(1), 10–14.

Rogaev, E. I., Iurov, I. B., & Iakovlev, A. G. (1992). [Molecular genetics of the human brain]. Vestn Ross Akad Med Nauk, (8), 11–16.

Ginter, E. K., Petrin, A. N., Spitsyn, V. A., & Rogaev, E. I. (1991). [An attempt to locate the gene for congenital cataracts using linkage analysis]. Genetika, 27(10), 1840–1849.

Rogaev, E. I., Shlenskii, A. B., & AYa, S. (1991). Individual-specific patterns of human variable genomic regions detected by a DNA probe from the HIV-1 env gene. Biomed Sci, 2(3), 311–313.

Nefedov, M. D., Gar'kavtsev, I. V., & Rogaev, E. I. (1990). [Analysis of the association of inherited predisposition to breast cancer with c-Ha-ras-1 oncogene alleles]. Genetika, 26(12), 2226–2231.

Rogaev, E. I., & Shlenskii, A. B. (1990). [DNA probe containing elements of the gene of surface glycoprotein of HIV-1 virus, an effective molecular marker in genotyposcopy of man]. Biull Eksp Biol Med, 110(12), 646–647.

Rogaev, E. I., & Shlenskii, A. V. (1990). [The test for the genomic DNA of bacteriophage FD 103 detects hypervariable regions in the human genome]. Biull Eksp Biol Med, 110(11), 525.

Rogaev, E. I., & Iurov, I. B. (1990). [Interindividual hyperpolymorphism of autosomal satellites III of human DNA]. Genetika, 26(8), 1532–1535.

Rogaev, E. I. (1990). Simple human DNA-repeats associated with genomic hypervariability, flanking the genomic retroposons and similar to retroviral sites. Nucleic Acids Res, 18(7), 1879–1885.

Rogaev, E. I., & Shlensky, A. B. (1990). The genomic DNA phi Fd103 probe is sensitive marker for detection of human hypervariable genomic regions. Nucleic Acids Res, 18(4), 1081.

Rogaev, E. I., Vetchinkina, A. A., & Iurov, I. B. (1989). Species specific variant of human centromeric DNA repeats: localization on chromosome 18 and recent amplification in human ancestral line. Mol Gen Mikrobiol Virusol, (4), 10–14.

Rogaev, E. I. (1989). Two novel human DNA tandem repeat families from the hypervariable DNA probe homologous to human apolipoprotein CII-gene intron and D. virilis satellite. Nucleic Acids Res, 17(3), 1246.

Rogaev, E. I. (1988 Sep-Oct). [The structure of genome region containing unstable elements of human DNA]. Dokl Akad Nauk SSSR, 302(1), 234–238.

Rogaev, E. I., & Shapiro, I. A. (1987). [High interindividual polymorphism in restriction fragment length and copy number of the TURI family of moderate human DNA repetitions]. Biull Eksp Biol Med, 103(1), 57–58.

Zaitsev, I. Z., & Rogaev, E. I. (1986 May-Jun). [Structural analysis of alphoid DNA of primates. II. Evolution and possible origin of alphoid DNA of primates]. Mol Biol (Mosk), 20(3), 674–682.

Zaitsev, I. Z., & Rogaev, E. I. (1986 May-Jun). [Structural analysis of alphoid DNA of primates. I. Heterogeneity of nucleotide sequence of alphoid repeats in human DNA]. Mol Biol (Mosk), 20(3), 663–673.