YB
Yury A. Barbitoff

Highly Cited

73
Works
1,065
Citations
19
H-Index
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Yury A. Barbitoff

Also known as: Barbitoff, Yury, Barbitoff, Yury A., Barbitoff, Yury, A, Y. A. Barbitoff, Y.A. Barbitoff

73

Total Works

1,065

Citations

19

H-Index

35

i10-Index

Citation & Works Trend by Year
11 years active
Top Research Topics
Genomics and Rare Diseases (33) Genetic Associations and Epidemiology (23) Genomics and Phylogenetic Studies (16) Prion Diseases and Protein Misfolding (10) Alzheimer's disease research and treatments (9)
Recent Publications
15 shown
Year Publication Title Citations Action
2026 Thousands of pathogenic variants in ClinVar show signs of incomplete loss-of-function Research Square 0
2026 High-impact Genetic Variants in EGLN1, EPAS1, and Other Genes Identified in Mountaineers by Exome Sequencing Frontiers in Bioscience-Scholar 0
2026 A systematic review on the generative AI applications in human medical genetics Frontiers in Genetics 4
2026 Understanding the interplay between positive and negative selection in the human genome IMAGINE - Repository of the Institute of molecular genetics and genetic engineering (University of Belgrade) 0
2025 Pilot Study of Preconception Carrier Screening in Russia: Initial Findings and Challenges Genes 2
2025 Functional Determinants and Evolutionary Consequences of Pleiotropy in Complex and Mendelian Traits Molecular Biology and Evolution 13
2025 Optimization of conditions for the productionof Hsp70 phaperones in Saccharomyces cerevisiae pells Ecological genetics 0
2025 PLoV: a comprehensive database of genetic variants leading to pregnancy loss Database 2
2024 Use of large-scale sample collections to estimate the carriage rate of miscarriage-related variants CARDIOVASCULAR THERAPY AND PREVENTION 0
2024 Deciphering the Transcriptomic Landscape of Type 2 Diabetes: Insights from Bulk RNA Sequencing and Single-Cell Analysis medRxiv 0
2024 Peer Review Report For: Negligible effects of read trimming on the accuracy of germline short variant calling in the human genome [version 1; peer review: 2 approved with reservations] 0
2024 Expanding the Russian allele frequency reference via cross-laboratory data integration: insights from 7452 exome samples National Science Review 56
2024 Peer Review Report For: Negligible effects of read trimming on the accuracy of germline short variant calling in the human genome [version 1; peer review: 2 approved with reservations] 0
2024 Major Causes of Conflicting Interpretations of Variant Pathogenicity in Rare Disease: A Systematic Analysis Journal of Personalized Medicine 9
2024 Replication of Known and Identification of Novel Associations in Biobank-Scale Datasets: A Survey Using UK Biobank and FinnGen Genes 9

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