Vasily Ramensky
Vasily Ramensky
National Medical Research Center for Preventive Medicine, Moscow, Russia
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A method and server for predicting damaging missense mutations
IA Adzhubei, S Schmidt, L Peshkin, VE Ramensky, A Gerasimova, P Bork, ...
Nature methods 7 (4), 248-249, 2010
Human non‐synonymous SNPs: server and survey
V Ramensky, P Bork, S Sunyaev
Nucleic acids research 30 (17), 3894-3900, 2002
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), eaap8757, 2018
Prediction of deleterious human alleles
S Sunyaev, V Ramensky, I Koch, W Lathe III, AS Kondrashov, P Bork
Human molecular genetics 10 (6), 591-597, 2001
Towards a structural basis of human non-synonymous single nucleotide polymorphisms
S Sunyaev, V Ramensky, P Bork
Trends in Genetics 16 (5), 198-200, 2000
Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome
AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ...
Neuron 94 (6), 1101-1111. e7, 2017
De novo coding variants are strongly associated with Tourette disorder
AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ...
Neuron 94 (3), 486-499. e9, 2017
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power
AE Locke, KM Steinberg, CWK Chiang, SK Service, AS Havulinna, L Stell, ...
Nature 575 (7783), E4-E4, 2019
Exome sequencing of Finnish isolates enhances rare-variant association power
AE Locke, KM Steinberg, CWK Chiang, SK Service, AS Havulinna, L Stell, ...
Nature 572 (7769), 323-328, 2019
De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis
S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ...
Cell reports 24 (13), 3441-3454. e12, 2018
The genome of the vervet (Chlorocebus aethiops sabaeus)
WC Warren, AJ Jasinska, R García-Pérez, H Svardal, C Tomlinson, ...
Genome research 25 (12), 1921-1933, 2015
Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum
The American Journal of Human Genetics 102 (6), 1204-1211, 2018
SNP frequencies in human genes: an excess of rare alleles and differing modes of selection
SR Sunyaev, WC Lathe Iii, VE Ramensky, P Bork
Trends in Genetics 16 (8), 335-337, 2000
Ancient hybridization and strong adaptation to viruses across African vervet monkey populations
H Svardal, AJ Jasinska, C Apetrei, G Coppola, Y Huang, CA Schmitt, ...
Nature Genetics, 2017
Human allelic variation: perspective from protein function, structure, and evolution
DM Jordan, VE Ramensky, SR Sunyaev
Current opinion in structural biology 20 (3), 342-350, 2010
Understanding the Hidden Complexity of Latin American Population Isolates
KEL JA Mooney, CD Huber, S Service, JH Sul, CD Marsden, Z Zhang, C Sabatti ...
American Journal of Human Genetics 103 (5), 707-726, 2018
A novel approach to local similarity of protein binding sites substantially improves computational drug design results
V Ramensky, A Sobol, N Zaitseva, A Rubinov, V Zosimov
Proteins: Structure, Function, and Bioinformatics 69 (2), 349-357, 2007
A retrocopy of a gene can functionally displace the source gene in evolution
AN Krasnov, MM Kurshakova, VE Ramensky, PV Mardanov, ...
Nucleic acids research 33 (20), 6654-6661, 2005
Maturation of the translation inhibitor microcin C
A Metlitskaya, T Kazakov, GH Vondenhoff, M Novikova, A Shashkov, ...
Journal of bacteriology 191 (7), 2380-2387, 2009
Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci
TM Teslovich, C Fuchsberger, V Ramensky, P Yajnik, DC Koboldt, ...
PLoS Genet 10 (1), e1004147, 2014
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