| 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 | 14564 | 2010 |
| Human non‐synonymous SNPs: server and survey V Ramensky, P Bork, S Sunyaev Nucleic acids research 30 (17), 3894-3900, 2002 | 2755 | 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 | 1456 | 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 | 1299 | 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 | 428 | 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 | 187 | 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 | 185 | 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 | 167* | 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 | 167 | 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 | 130 | 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 | 121 | 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 | 115 | 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 | 105 | 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 | 95 | 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 | 89 | 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 | 60 | 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 | 56 | 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 | 55 | 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 | 51 | 2009 |
| The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia A Meshkov, A Ershova, A Kiseleva, E Zotova, E Sotnikova, A Petukhova, ... Genes 12 (1), 66, 2021 | 48 | 2021 |
Shamil SunyaevProfessor of Biomedical Informatics and of Medicine (BWH), Harvard Medical SchoolVerified email at rics.bwh.harvard.edu
