Mykyta Artomov
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
108
Citations
4,304
Est. group size
~3
Recurring co-author estimate
Active years
17
Publishing since 2010
Mykyta Artomov works in human genetics and genomics, using large-scale genetic association studies (like GWAS and exome sequencing) to find gene variants linked to diseases such as autism, kidney disease, cancer, and cardiovascular conditions. Much of the work involves developing computational and statistical methods for analyzing genetic data across large populations, sometimes without needing to share raw genetic data between institutions. This research could suit students interested in bioinformatics, statistical genetics, or genomic medicine applied to psychiatric, oncological, or cardiovascular conditions.
Publication output has grown substantially over the last decade, rising from about 5 papers per year around 2017-2018 to a peak of 30 in 2023, with continued high output (9-21 papers/year) through 2024-2026.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Deleterious coding variation associated with autism is shared across ancestries
Nature Medicine · 2026
- Treatment of hypertensive patients in Russian real-world practice based on the data from 2025 blood pressure measurement campaign
Russian Journal of Cardiology · 2025
- Cost-effective non-additive GWAS across 2329 diseases in 500,349 individuals
Nature Communications · 2025
- CR1 variants contribute to FSGS susceptibility across multiple populations
iScience · 2025
- SEX DIFFERENCES OF “HEART STRESS” IN 200 ASYMPTOMATIC INDIVIDUALS FROM THE POPULATION-BASED SAMPLE
Journal of Hypertension · 2025
- Insulin/IGF-1 signaling modulation in prefrontal cortex is linked to antisuicidal effects in MDD
Research Square · 2025
- Germline cancer susceptibility in individuals with melanoma
Journal of the American Academy of Dermatology · 2024
- Public platform with 39,472 exome control samples enables association studies without genotype sharing
Nature Genetics · 2024
- 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 · 2024
- Whole-exome sequencing reveals an association of rs112065068 in TGOLN2 gene with distant metastasis of non-small cell lung cancer
Gene · 2024
- Genetics of healthy aging and longevity
Arterial’naya Gipertenziya (Arterial Hypertension) · 2024
- THE ASSOCIATION OF SERUM URIC ACID LEVELS WITH CARDIOVASCULAR MORBIDITY AND MORTALITY
Journal of Hypertension · 2024
- DEEP LEARNING MODELS FOR PREDICTING THE RISK OF CARDIOVASCULAR INCIDENTS BASED ON THE WISCONSIN LONGITUDINAL STUDY
Journal of Hypertension · 2024
- Case report: A case study of variant calling pipeline selection effect on the molecular diagnostics outcome
Frontiers in Oncology · 2024
- Mendelian Randomization Analysis reveals Inverse Genetic Risks between Skin Cancers and Vitiligo
JID Innovations · 2023
- bioRxiv (Cold Spring Harbor Laboratory)×12
- Journal of Hypertension×11
- medRxiv×5
- Scientific Reports×4
- Nature Communications×4
- Sarah E. Wolf
Biochemistry, Genetics and Molecular Biology · Indiana University
- Jennifer Wessel
Biochemistry, Genetics and Molecular Biology · Indiana University
- Taeho Jo
Biochemistry, Genetics and Molecular Biology · Indiana University
- Yun Li
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Alexander Gusev
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
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