Yulia A. Nasykhova

486 total citations
32 papers, 240 citations indexed

About

Yulia A. Nasykhova is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yulia A. Nasykhova has authored 32 papers receiving a total of 240 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yulia A. Nasykhova's work include Pregnancy and preeclampsia studies (6 papers), Genetic Associations and Epidemiology (6 papers) and Genomics and Rare Diseases (5 papers). Yulia A. Nasykhova is often cited by papers focused on Pregnancy and preeclampsia studies (6 papers), Genetic Associations and Epidemiology (6 papers) and Genomics and Rare Diseases (5 papers). Yulia A. Nasykhova collaborates with scholars based in Russia, United Kingdom and Italy. Yulia A. Nasykhova's co-authors include Аndrey S. Glotov, Yury A. Barbitoff, Elena S. Vashukova, Alexander V. Predeus, Dmitriy Katserov, Oleg S. Glotov, Dmitrii E. Polev, Olesya N. Bespalova, Irina Shcherbakova and Anastasia Efimenko and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Briefings in Bioinformatics.

In The Last Decade

Yulia A. Nasykhova

27 papers receiving 228 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Yulia A. Nasykhova Russia 11 87 74 49 39 39 32 240
Laura B. L. Wittemans United Kingdom 7 106 1.2× 98 1.3× 92 1.9× 55 1.4× 47 1.2× 9 415
Eiichiro Satake Japan 10 159 1.8× 48 0.6× 59 1.2× 101 2.6× 41 1.1× 25 348
Seong Beom Cho South Korea 9 92 1.1× 55 0.7× 44 0.9× 16 0.4× 30 0.8× 19 283
Thutrang Nguyen United States 7 63 0.7× 114 1.5× 132 2.7× 20 0.5× 33 0.8× 9 375
Cecilia Catellani Italy 9 100 1.1× 28 0.4× 40 0.8× 93 2.4× 15 0.4× 17 300
Wanee Plengpanich Thailand 12 88 1.0× 46 0.6× 109 2.2× 50 1.3× 108 2.8× 22 305
Biswabandhu Bankura India 12 113 1.3× 26 0.4× 61 1.2× 19 0.5× 41 1.1× 28 293
Hamid Farahani Iran 13 65 0.7× 30 0.4× 109 2.2× 46 1.2× 27 0.7× 32 329
David T. Duong United States 7 131 1.5× 82 1.1× 40 0.8× 24 0.6× 80 2.1× 8 348

Countries citing papers authored by Yulia A. Nasykhova

Since Specialization
Citations

This map shows the geographic impact of Yulia A. Nasykhova's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yulia A. Nasykhova with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yulia A. Nasykhova more than expected).

Fields of papers citing papers by Yulia A. Nasykhova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yulia A. Nasykhova. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yulia A. Nasykhova. The network helps show where Yulia A. Nasykhova may publish in the future.

Co-authorship network of co-authors of Yulia A. Nasykhova

This figure shows the co-authorship network connecting the top 25 collaborators of Yulia A. Nasykhova. A scholar is included among the top collaborators of Yulia A. Nasykhova based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yulia A. Nasykhova. Yulia A. Nasykhova is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Barbitoff, Yury A., et al.. (2025). PLoV: a comprehensive database of genetic variants leading to pregnancy loss. Database. 2025.
3.
Barbitoff, Yury A., et al.. (2024). Bioinformatics of germline variant discovery for rare disease diagnostics: current approaches and remaining challenges. Briefings in Bioinformatics. 25(2). 7 indexed citations
4.
Barbitoff, Yury A., et al.. (2024). Major Causes of Conflicting Interpretations of Variant Pathogenicity in Rare Disease: A Systematic Analysis. Journal of Personalized Medicine. 14(8). 864–864. 2 indexed citations
5.
Barbitoff, Yury A., et al.. (2023). Statistical Dissection of the Genetic Determinants of Phenotypic Heterogeneity in Genes with Multiple Associated Rare Diseases. Genes. 14(11). 2100–2100. 3 indexed citations
6.
Vashukova, Elena S., et al.. (2023). Inventory and quality control of biosample collection from pregnant women at different gestational ages to search for early biomarkers of pregnancy complications. CARDIOVASCULAR THERAPY AND PREVENTION. 22(11). 3740–3740. 1 indexed citations
7.
8.
Barbitoff, Yury A., et al.. (2023). The Landscape of Point Mutations in Human Protein Coding Genes Leading to Pregnancy Loss. International Journal of Molecular Sciences. 24(24). 17572–17572. 2 indexed citations
9.
Glotov, Аndrey S., et al.. (2023). Prospects for preconception genetic screening at the pregnancy planning stage. Journal of obstetrics and women s diseases. 72(6). 173–192. 1 indexed citations
10.
Barbitoff, Yury A., et al.. (2023). Plasma microRNA Profiling in Type 2 Diabetes Mellitus: A Pilot Study. International Journal of Molecular Sciences. 24(24). 17406–17406. 7 indexed citations
11.
Nasykhova, Yulia A., et al.. (2022). Overview of Transcriptomic Research on Type 2 Diabetes: Challenges and Perspectives. Genes. 13(7). 1176–1176. 14 indexed citations
12.
Glotov, Аndrey S., Yulia A. Nasykhova, Yury A. Barbitoff, et al.. (2022). Prospects for biobanking in reproductive health: genetic aspects. Biological Communications. 67(4). 1 indexed citations
13.
14.
Nasykhova, Yulia A., et al.. (2022). Genetic and Phenotypic Factors Affecting Glycemic Response to Metformin Therapy in Patients with Type 2 Diabetes Mellitus. Genes. 13(8). 1310–1310. 10 indexed citations
15.
Barbitoff, Yury A., et al.. (2022). Biobanking as a Tool for Genomic Research: From Allele Frequencies to Cross-Ancestry Association Studies. Journal of Personalized Medicine. 12(12). 2040–2040. 12 indexed citations
16.
Barbitoff, Yury A., et al.. (2022). Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Genes. 13(12). 2255–2255. 10 indexed citations
17.
Barbitoff, Yury A., Yulia A. Nasykhova, Dmitrii E. Polev, et al.. (2019). Whole‐exome sequencing provides insights into monogenic disease prevalence in Northwest Russia. Molecular Genetics & Genomic Medicine. 7(11). 25 indexed citations
18.
Barbitoff, Yury A., Yulia A. Nasykhova, Alexander V. Predeus, et al.. (2018). Identification of Novel Candidate Markers of Type 2 Diabetes and Obesity in Russia by Exome Sequencing with a Limited Sample Size. Genes. 9(8). 415–415. 24 indexed citations
19.
Nasykhova, Yulia A., et al.. (2014). PHENOTYPIC CHARACTERISTICS AND GENETIC HETEROGENEITY IN PATIENTS WITH LATE-ONSET UNCLASSICAL CYSTIC FIBROSIS. PULMONOLOGIYA. 66–70. 1 indexed citations
20.
Glotov, Аndrey S., et al.. (2014). Study of the population frequencies of gene polymorphisms, associated with preeclampsia. Russian Journal of Genetics Applied Research. 4(5). 388–396. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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