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Институт персонализированной терапии и профилактики
Лаборатория геномной и медицинской биоинформатики
Основные публикации

Основные публикации

Зайченока М, Ершова АИ, Киселева АВ, et al (2023) Поиск и репликация ассоциаций вариантов генома с уровнями липидов в выборке из представителей российской популяции. Кардиоваскулярная терапия и профилактика 22:3871
Azbukina N, Zharikova A, Ramensky V (2022) Intragenic compensation through the lens of deep mutational scanning. Biophys Rev. https://doi.org/10.1007/s12551-022-01005-w
Blokhina AV, Ershova AI, Meshkov AN, et al (2022) Phenotypic vs. genetic cascade screening for familial hypercholesterolemia: A case report. Frontiers in Cardiovascular Medicine 9:
Gress A, Srikakulam SK, Keller S, et al (2022) d-StructMAn: Containerized structural annotation on the scale from genetic variants to whole proteomes. GigaScience 11:giac086. https://doi.org/10.1093/gigascience/giac086
Limonova AS, Ershova AI, Kiseleva AV, et al (2023) Assessment of polygenic risk of hypertension. Cardiovasc Ther Prev 21:3464. https://doi.org/10.15829/1728-8800-2022-3464
Locke AE, Steinberg KM, Chiang CWK, et al (2019) Exome sequencing of Finnish isolates enhances rare-variant association power. Nature 572:323–328. https://doi.org/10.1038/s41586-019-1457-z
Meshkov A, Ershova A, Kiseleva A, et al (2021) The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia. Genes 12:66. https://doi.org/10.3390/genes12010066
Myasnikov R, Bukaeva A, Kulikova O, et al (2022) A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene. Genes 13:309. https://doi.org/10.3390/genes13020309
Ramensky VE, Ershova AI, Zaicenoka M, et al (2021) Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region. Frontiers in Genetics 12:1782. https://doi.org/10.3389/fgene.2021.709419
Schmitt CA, Bergey CM, Jasinska AJ, et al (2020) ACE2 and TMPRSS2 variation in savanna monkeys (Chlorocebus spp.): Potential risk for zoonotic/anthroponotic transmission of SARS-CoV-2 and a potential model for functional studies. PLoS ONE 15:e0235106. https://doi.org/10.1371/journal.pone.0235106
Shah Z, Filonenko ES, Ramensky V, et al (2021) MYB bi-allelic targeting abrogates primitive clonogenic progenitors while the emergence of primitive blood cells is not affected. Haematologica 106:2191–2202. https://doi.org/10.3324/haematol.2020.249193
Sotnikova EA, Kiseleva AV, Kutsenko VA, et al (2022) Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases. Journal of Personalized Medicine 12:1132. https://doi.org/10.3390/jpm12071132
Sul JH, Service SK, Huang AY, et al (2020) Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates. Transl Psychiatry 10:1–10. https://doi.org/10.1038/s41398-020-0758-1
Лимонова АС, Ершова АИ, Мешков АН, et al (2022) Полигенный Риск Артериальной Гипертензии: Воспроизводимость Европейский Шкал Генетического Риска У Жителей Центральной России. Кардиоваскулярная Терапия И Профилактика 21:
Мешков АИ, Киселева АВ, Ершова АИ, et al (2022) Варианты Генов Angptl3, Angptl4, Apoa5, Apob, Apoc2, Apoc3, Ldlr, Pcsk9, Lpl И Риск Ишемической Болезни Сердца. Российский Кардиологический Журнал 27:. https://doi.org/10.15829/1560-4071-2022-5232