Mykyta Artomov

Nationwide Children's Hospital — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index4.0kcitations104works3.12yr avg
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Research Topics

Genomics and Rare Diseases(16), Genetic Associations and Epidemiology(15), Histone Deacetylase Inhibitors Research(15), Cancer Genomics and Diagnostics(14), Epigenetics and DNA Methylation(11)

Publications104 total

Germline inactivation of tumor suppressor BAP1 is associated with white spotting
Journal of Clinical Investigation·2026Open Access
Cost-effective non-additive GWAS across 2329 diseases in 500,349 individuals
Nature Communications·2025Open Access
Treatment of hypertensive patients in Russian real-world practice based on the data from 2025 blood pressure measurement campaign
Russian Journal of Cardiology·2025Open Access
Mendelian randomization analysis provides insights into the relationship between inflammatory bowel disease and skin cancer
Molecular and Clinical Oncology·2025Open Access
PGS Browser: a public platform for personalized polygenic score interpretation
2025Open Access
Method for identifying the active module in biological graphs with multi-component vertex weights
Scientific and technical journal of information technologies mechanics and optics·2025Open Access
Insulin/IGF-1 signaling modulation in prefrontal cortex is linked to antisuicidal effects in MDD
2025Open Access
Analysis of vascular aging phenotypes in a high cardiovascular risk population
Scientific Reports·2025Open Access
SEX DIFFERENCES OF “HEART STRESS” IN 200 ASYMPTOMATIC INDIVIDUALS FROM THE POPULATION-BASED SAMPLE
Journal of Hypertension·2025
CR1 variants contribute to FSGS susceptibility across multiple populations
iScience·2025· 1 citedOpen Access
Analysis of Variants Induced by Combined Ex Vivo Irradiation and In Vivo Tumorigenesis Suggests a Role for the ZNF831 p.R1393Q Variant in Cutaneous Melanoma Development
Journal of Investigative Dermatology·2024· 1 cited
The effect size of rs521851 in the intron of MAGI2/S-SCAM on HADS-D scores correlates with EAT-26 scores for eating disorders risk
Frontiers in Psychiatry·2024Open Access
Making sense of missense: challenges and opportunities in variant pathogenicity prediction
Disease Models & Mechanisms·2024· 7 citedOpen Access
Application of Markov chain Monte Carlo and machine learning for identifying active modules in biological graphs
Scientific and technical journal of information technologies mechanics and optics·2024· 1 citedOpen Access
Case report: A case study of variant calling pipeline selection effect on the molecular diagnostics outcome
Frontiers in Oncology·2024Open Access
Characterization of pathogenic genetic variants in Russian patients with primary ciliary dyskinesia using gene panel sequencing and transcript analysis
Orphanet Journal of Rare Diseases·2024· 6 citedOpen Access
Primary murine high-grade glioma cells derived from RCAS/tv-a diffuse glioma model reprogram naive T cells into immunosuppressive regulatory T lymphocytes
Molecular Therapy Oncology·2024· 1 citedOpen Access
Complex trait susceptibilities and population diversity in a sample of 4,145 Russians
Nature Communications·2024· 12 citedOpen Access
The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis
Journal of Cardiovascular Development and Disease·2024· 4 citedOpen Access
Autoimmune hypothyroidism GWAS reveals independent autoimmune and thyroid-specific contributions and an inverse relation with cancer risk
2024· 10 citedOpen Access
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Frequent Co-authors

Mark J. Daly(29), Aarno Palotie(10), Hensin Tsao(9), Anna Kostareva(9), А. О. Конради(8), Nikita Kolosov(8), Giulio Genovese(6), Dmitrii Usoltsev(6), Christine Stevens(5), Mitja Kurki(5), Benjamin M. Neale(5), Alexander Loboda(5), M. Boyarinova(5), Е. П. Колесова(5), Valeriia Rezapova(5), Rostislav Skitchenko(5), Alexey Sergushichev(5), Е. V. Shlyakhto(5), F. Kyle Satterstrom(4), Minshi Peng(4)