Get started
Author

Yury A. Barbitoff

Observed names: Barbitoff, Yury, Barbitoff, Yury A., Barbitoff, Yury, A, Y. A. Barbitoff, Y.A. Barbitoff, Yu. A. Barbitov, Yu.A. Barbitoff, Yury A Barbitoff, Yury Barbitoff
Observed institutions: St Petersburg University, Stockholm School of Economics in Russia, University of Belgrade, Research Institute of Obstetrics and Gynecology named after D.O. Ott, Bioinformatics Institute, Bioinformatics Institute
ORCID: 0000-0002-3222-440X
Observed ORCID: 0000-0002-3222-440X
OpenAlex ID: A5050468948
Systematic dissection of biases in whole-exome and whole-genome sequencing reveals major determinants of coding sequence coverage
2020 · Yury A. Barbitoff, Dmitrii E. Polev, et al. · Scientific Reports · 150
PDF
Systematic benchmark of state-of-the-art variant calling pipelines identifies major factors affecting accuracy of coding sequence variant discovery
2022 · Ruslan Abasov, Varvara E. Tvorogova, et al. · BMC Genomics · 109
PDF
Expanding the Russian allele frequency reference via cross-laboratory data integration: insights from 7452 exome samples
2024 · Yury A Barbitoff, Darya N Khmelkova, et al. · National Science Review · 61
PDF
Analysis of the Spectrum of ACE2 Variation Suggests a Possible Influence of Rare and Common Variants on Susceptibility to COVID-19 and Severity of Outcome
2020 · Anton E. Shikov, Yury A. Barbitoff, et al. · Frontiers in Genetics · 41
PDF
Phenome-wide functional dissection of pleiotropic effects highlights key molecular pathways for human complex traits
2020 · Anton E. Shikov, Rostislav K. Skitchenko, et al. · Scientific Reports · 40
PDF
Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes
2019 · Oleg Glotov, Elena Serebryakova, et al. · Molecular Medicine Reports · 36
PDF
A Data-Driven Review of the Genetic Factors of Pregnancy Complications
2020 · Yury A. Barbitoff, Alexander A. Tsarev, et al. · International Journal of Molecular Sciences · 35
PDF
Amyloid and Amyloid-Like Aggregates: Diversity and the Term Crisis
2020 · A. B. Matiiv, N. P. Trubitsina, et al. · Biochemistry (Moscow) · 33
PDF
Whole‐exome sequencing provides insights into monogenic disease prevalence in Northwest Russia
2019 · Yury A. Barbitoff, Rostislav K. Skitchenko, et al. · Molecular Genetics & Genomic Medicine · 33
PDF
Differential effects of chaperones on yeast prions: CURrent view
2017 · Andrew G. Matveenko, Yury A. Barbitoff, et al. · Current Genetics · 32
Catching hidden variation: systematic correction of reference minor allele annotation in clinical variant calling
2017 · Yury A. Barbitoff, Igor V. Bezdvornykh, et al. · Genetics in Medicine · 31
PDF
Identification of Novel Candidate Markers of Type 2 Diabetes and Obesity in Russia by Exome Sequencing with a Limited Sample Size
2018 · Yury A. Barbitoff, Elena A. Serebryakova, et al. · Genes · 29
PDF
To CURe or not to CURe? Differential effects of the chaperone sorting factor Cur1 on yeast prions are mediated by the chaperone Sis1
2017 · Yury A. Barbitoff, Andrew G. Matveenko, et al. · Molecular Microbiology · 29
PDF
Bioinformatics of germline variant discovery for rare disease diagnostics: current approaches and remaining challenges
2023 · Yury A Barbitoff, Mikhail O Ushakov, et al. · Briefings in Bioinformatics · 28
PDF
Recent advances and perspectives in next generation sequencing application to the genetic research of type 2 diabetes
2019 · Yulia A Nasykhova, Yury A Barbitoff, et al. · World Journal of Diabetes · 28
PDF
Overview of Transcriptomic Research on Type 2 Diabetes: Challenges and Perspectives
2022 · Ziravard N. Tonyan, Yulia A. Nasykhova, et al. · Genes · 27
PDF
Identification of novel variants in the LDLR gene in Russian patients with familial hypercholesterolemia using targeted sequencing
2020 · Valentina Miroshnikova, Olga Romanova, et al. · Biomedical Reports · 26
PDF
The spectrum of pathogenic variants of the ATP7B gene in Wilson disease in the Russian Federation
2019 · Mariya S. Balashova, Inna G. Tuluzanovskaya, et al. · Journal of Trace Elements in Medicine and Biology · 21
Biobanking as a Tool for Genomic Research: From Allele Frequencies to Cross-Ancestry Association Studies
2022 · Tatyana E. Lazareva, Yury A. Barbitoff, et al. · Journal of Personalized Medicine · 20
PDF
Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications
2022 · Anton Changalidis, Evgeniia Maksiutenko, et al. · Genes · 20
PDF
Genetic and Phenotypic Factors Affecting Glycemic Response to Metformin Therapy in Patients with Type 2 Diabetes Mellitus
2022 · Yulia Nasykhova, Yury Barbitoff, et al. · Genes · 19
PDF
Molecular Genetics and Pathogenesis of the Floating Harbor Syndrome: Case Report of Long-Term Growth Hormone Treatment and a Literature Review
2022 · Mariia E. Turkunova, Yury A. Barbitoff, et al. · Frontiers in Genetics · 18
SFP1‐mediated prion‐dependent lethality is caused by increased Sup35 aggregation and alleviated by Sis1
2016 · Andrew G. Matveenko, Polina B. Drozdova, et al. · Genes to Cells · 18
Functional Determinants and Evolutionary Consequences of Pleiotropy in Complex and Mendelian Traits
2025 · Yury A Barbitoff, Polina M Bogaichuk, et al. · Molecular Biology and Evolution · 16
PDF
Annotation of uORFs in the OMIM genes allows to reveal pathogenic variants in 5′UTRs
2022 · Alexandra Filatova, Ivan Reveguk, et al. · Nucleic Acids Research · 16
PDF
Works count: 71
Citation count: 1,135
H-index: 20
I10-index: 38
Year
Topic
Type