Human non‐synonymous SNPs: server and survey von Ramensky, Vasily, Bork, Peer, Sunyaev, Shamil

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Biologist Nikolai K. Koltzoff: the forgotten genius von Ptushenko, Vasily V, Ramensky, Evgeny V

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Spatial distribution of disease-associated variants in three-dimensional structures of protein complexes von Gress, A, Ramensky, V, Kalinina, O V

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Comparative analysis of bioelectric activity of the brain of ambulance station personnel before and after daily duty von Smolyakov, Yu. N., Ramensky, V. V., Nolfin, N. A., Anokhova, L. I., Fedorenko, E. V., Mikhahanov, M. M.

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Search and replication of associations of genome variants with lipid levels in a Russian sample von Zaichenoka, M., Ershova, A. I., Kiseleva, A. V., Sotnikova, E. A., Vyatkin, Yu. V., Zharikova, А. A., Pokrovskaya, M. S., Shalnova, S. A., Ramensky, V. E., Meshkov, A. N., Drapkina, O. M.

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Validation of genetic risk scores for hypertension in the Central Russian population von Limonova, A. S., Ershova, A. I., Kiseleva, A. V., Kutsenko, V. A., Ramensky, V. E., Vyatkin, Yu. V., Sotnikova, E. A., Zharikova, A. A., Zaichenoka, M., Pokrovskaya, M. S., Shalnova, S. А., Meshkov, A. N., Drapkina, O. M.

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Assessment of polygenic risk of hypertension von Limonova, A. S., Ershova, A. I., Kiseleva, A. V., Ramensky, V. E., Vyatkin, Yu. V., Kutsenko, V. A., Meshkov, A. N., Drapkina, O. M.

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Validation of genetic risk scores for coronary artery disease, developed on European population samples, in Russian population von Ershova, A. I., Meshkov, A. N., Kutsenko, V. A., Vyatkin, Yu. V., Kiseleva, A. V., Sotnikova, E. A., Limonova, A. S., Garbuzova, E. V., Muromtseva, G. A., Zaicenoka, M., Zharikova, A. A., Ramensky, V. E., Belova, O. А., Rachkova, S. A., Pokrovskaya, M. S., Shalnova, S. A., Boytsov, S. A., Drapkina, O. M.

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Genetic aspects of decreased low-density lipoprotein cholesterol values von Meshkov, A. N., Ershova, A. I., Kiseleva, A. V., Mikhailina, V. I., Smetnev, S. A., Soplenkova, А. G., Kutsenko, V. A., Sotnikova, Е. A., Vyatkin, Yu. V., Zharikova, A. A., Zaichenoka, M., Ramensky, V. E., Skirko, O. P., Pokrovskaya, M. S., Litinskaya, O. A., Shalnova, S. A., Drapkina, O. M.

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Validation of genetic risk scores for type 2 diabetes on a Russian population sample from the biobank of the National Medical Research Center for Therapy and Preventive Medicine von Kiseleva, A. V., Soplenkova, A. G., Kutsenko, V. A., Sotnikova, E. A., Vyatkin, Yu. V., Zharikova, А. A., Ershova, A. I., Zaichenoka, M., Ramensky, V. E., Skirko, O. P., Smetnev, S. А., Kopylova, O. V., Limonova, А. S., Blokhina, A. V., Pokrovskaya, M. S., Shalnova, S. A., Meshkov, A. N., Drapkina, O. M.

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Validation of genetic risk scores for obesity on a sample of the population of Russian regions von Kiseleva, A. V., Soplenkova, A. G., Kutsenko, V. A., Sotnikova, E. A., Vyatkin, Yu. V., Zharikova, А. A., Ershova, A. I., Zaichenoka, M., Ramensky, V. E., Skirko, O. P., Smetnev, S. А., Kopylova, O. V., Limonova, А. S., Blokhina, A. V., Pokrovskaya, M. S., Shalnova, S. A., Meshkov, A. N., Drapkina, O. M.

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ANGPTL3, ANGPTL4, APOA5, APOB, APOC2, APOC3, LDLR, PCSK9, LPL gene variants and coronary artery disease risk von Meshkov, A. N., Kiseleva, A. V., Ershova, A. I., Sotnikova, E. A., Smetnev, S. A., Limonova, A. S., Zharikova, A. A., Zaychenoka, M., Ramensky, V. E., Drapkina, O. M.

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Carotid and femoral plaques in patients with familial dysbetalipoproteinemia, familial hypercholesterolemia, polygenic and severe hypercholesterolemia von Blokhina, A., Ershova, A., Kiseleva, A., Sotnikova, E., Zharikova, A., Zaicenoka, M., Vyatkin, Y., Ramensky, V., Kutsenko, V., Meshkov, A., Drapkina, O.

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The prevalence of familial dysbetalipoproteinemia in one of the European regions of the Russian Federation von Blokhina, A., Ershova, A., Kiseleva, A., Sotnikova, E., Zharikova, A., Zaicenoka, M., Vyatkin, Y., Ramensky, V., Kutsenko, V., Shalnova, S., Meshkov, A., Drapkina, O.

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Towards a structural basis of human non-synonymous single nucleotide polymorphisms von Sunyaev, S, Ramensky, V, Bork, P

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Prediction of deleterious human alleles von Sunyaev, S, Ramensky, V, Koch, I, Lathe, 3rd, W, Kondrashov, A S, Bork, P

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Computational analysis of human genome polymorphism von Ramensky, V. E, Sunyaev, S. R

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SNP frequencies in human genes: an excess of rare alleles and differing modes of selection von Sunyaev, Shamil R., Lathe III, Warren C., Ramensky, Vasily E., Bork, Peer

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DNA segmentation through the Bayesian approach von Ramensky, V E, Makeev VJu, Roytberg, M A, Tumanyan, V G

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Exome sequencing of Finnish isolates enhances rare-variant association power von Locke, AE, Steinberg, KM, Chiang, CWK, Service, SK, Havulinna, AS, Stell, L, Pirinen, M, Abel, HJ, Chiang, CC, Fulton, RS, Jackson, AU, Kang, CJ, Kanchi, KL, Koboldt, DC, Larson, DE, Nelson, J, Nicholas, TJ, Pietila, A, Ramensky, V, Ray, D, Scott, LJ, Stringham, HM, Vangipurapu, J, Welch, R, Yajnik, P, Yin, X, Eriksson, JG, Ala-Korpela, M, Jarvelin, M-R, Mannikko, M, Laivuori, H, Dutcher, SK, Stitziel, NO, Wilson, RK, Hall, IM, Sabatti, C, Palotie, A, Salomaa, V, Laakso, M, Ripatti, S, Boehnke, M, Freimer, NB

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