Vasily Ramensky

- Genetics of monogenic and complex human diseases
- Computational analysis of the effects of genome variants
- Study of the mechanisms of intragenic compensation of pathogenic mutations in humans and mutations that cause resistance in bacteria
- Structural bioinformatics

1. Ramensky V, Ershova AI, Zaicenoka M, et al. Targeted sequencing of 242 clinically important genes in the Russian population from the Ivanovo region. Front. Genet. 2021, in press. doi: 10.3389/fgene.2021.709419

2. Locke AE, Steinberg KM, Chiang CWK, et al. Exome sequencing of Finnish isolates enhances rare-variant association power. Nature. 2019 Aug;572(7769):323-328. doi: 10.1038/s41586-019-1457-z. Epub 2019 Jul 31. Erratum in: Nature. 2019 Nov;575(7783):E4. PMID: 31367044; PMCID: PMC6697530.

3. Svardal H, Jasinska AJ, Apetrei C, et al. Ancient hybridization and strong adaptation to viruses across African vervet monkey populations. Nat Genet. 2017 Dec;49(12):1705-1713. doi: 10.1038/ng.3980. Epub 2017 Oct 30. Erratum in: Nat Genet. 2018 Nov;50(11):1617. PMID: 29083404; PMCID: PMC5709169.

4. Gress A, Ramensky V, Kalinina OV. Spatial distribution of disease-associated variants in three-dimensional structures of protein complexes. Oncogenesis. 2017 Sep 25;6(9):e380. doi: 10.1038/oncsis.2017.79. PMID: 28945216; PMCID: PMC5623905.

5. Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR. A method and server for predicting damaging missense mutations. Nat Methods. 2010 Apr;7(4):248-9. doi: 10.1038/nmeth0410-248. PMID: 20354512; PMCID: PMC2855889.

6. Ramensky VE, Nurtdinov RN, Neverov AD, Mironov AA, Gelfand MS. Positive selection in alternatively spliced exons of human genes. Am J Hum Genet. 2008 Jul;83(1):94-8. doi: 10.1016/j.ajhg.2008.05.017. Epub 2008 Jun 19. PMID: 18571144; PMCID: PMC2443848.

7. Ramensky V, Bork P, Sunyaev S. Human non-synonymous SNPs: server and survey. Nucleic Acids Res. 2002 Sep 1;30(17):3894-900. doi: 10.1093/nar/gkf493. PMID: 12202775; PMCID: PMC137415.