Р. А. Зинченко

1.5k total citations
206 papers, 972 citations indexed

About

Р. А. Зинченко is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Р. А. Зинченко has authored 206 papers receiving a total of 972 indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 57 papers in Genetics and 27 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Р. А. Зинченко's work include Nutrition, Genetics, and Disease (24 papers), Cystic Fibrosis Research Advances (23 papers) and Regional Socio-Economic Development Trends (23 papers). Р. А. Зинченко is often cited by papers focused on Nutrition, Genetics, and Disease (24 papers), Cystic Fibrosis Research Advances (23 papers) and Regional Socio-Economic Development Trends (23 papers). Р. А. Зинченко collaborates with scholars based in Russia, United Kingdom and United States. Р. А. Зинченко's co-authors include Andrey V. Marakhonov, Tatyana A. Vasilyeva, Sergey I. Kutsev, E. K. Ginter, A. A. Voskresenskaya, Ginter Ek, Н.В. Петрова, A. V. Polyakov, Andrey Goltsov and Е. И. Рогаев and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Р. А. Зинченко

172 papers receiving 958 citations

Peers

Р. А. Зинченко
Andrey V. Marakhonov Russia
Solaf M. Elsayed Egypt
Katta M. Girisha India
Katrina M. Bell Australia
Deborah Tamura United States
Arne König Germany
Xiao Hui Liao United States
Mohsen Ghadami Iran
Sylvie Manouvrier France
Martine Doco‐Fenzy France
Andrey V. Marakhonov Russia
Р. А. Зинченко
Citations per year, relative to Р. А. Зинченко Р. А. Зинченко (= 1×) peers Andrey V. Marakhonov

Countries citing papers authored by Р. А. Зинченко

Since Specialization
Citations

This map shows the geographic impact of Р. А. Зинченко'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 Р. А. Зинченко with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Р. А. Зинченко more than expected).

Fields of papers citing papers by Р. А. Зинченко

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Р. А. Зинченко. 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 Р. А. Зинченко. The network helps show where Р. А. Зинченко may publish in the future.

Co-authorship network of co-authors of Р. А. Зинченко

This figure shows the co-authorship network connecting the top 25 collaborators of Р. А. Зинченко. A scholar is included among the top collaborators of Р. А. Зинченко 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 Р. А. Зинченко. Р. А. Зинченко 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.
Mukhinа, Anna, Dmitry Pershin, Dmitry Meleshko, et al.. (2025). 13q Deletion Syndrome Presenting with Lymphopenia Detected Through Newborn Screening for Primary Immunodeficiencies. International Journal of Molecular Sciences. 26(19). 9302–9302.
2.
3.
Вейко, Н. Н., et al.. (2025). Copy Number Variations of Human Ribosomal Genes in Health and Disease: Role and Causes. Frontiers in Bioscience-Landmark. 30(2). 25765–25765.
4.
Marakhonov, Andrey V., et al.. (2024). Genetic Landscape and Clinical Features of Hyperphenylalaninemia in North Ossetia-Alania: High Frequency of P281L and P211T Genetic Variants in the PAH Gene. International Journal of Molecular Sciences. 25(9). 4598–4598. 2 indexed citations
5.
Vasilyeva, Tatyana A., et al.. (2024). Clinical and Molecular Findings in Patients with Knobloch Syndrome 1: Case Series Report. Genes. 15(10). 1295–1295. 1 indexed citations
6.
Marakhonov, Andrey V., et al.. (2024). The Study of the Inheritance Mechanisms of Myotonic Dystrophy Type 1 (DM1) in Families from the Republic of North Ossetia-Alania. International Journal of Molecular Sciences. 25(17). 9734–9734. 2 indexed citations
7.
Зинченко, Р. А., et al.. (2024). Development of a Vector Finder Toolkit for Track Reconstruction at NICA Experiments: Current Status and Future Prospects. Physics of Particles and Nuclei. 55(4). 811–816.
8.
Marakhonov, Andrey V., et al.. (2024). Masks of Albinism: Clinical Spectrum of Hermansky–Pudlak Syndrome. International Journal of Molecular Sciences. 25(20). 11260–11260.
9.
Kashirskaya, N., E. Kondratyeva, Т. Б. Бухарова, et al.. (2024). Comprehensive Assessment of CFTR Modulators’ Therapeutic Efficiency for N1303K Variant. International Journal of Molecular Sciences. 25(5). 2770–2770. 3 indexed citations
10.
Зинченко, Р. А., et al.. (2023). Gender differentiation of interethnic marriages of the population of the North Caucasus. Nauchno-prakticheskii zhurnal «Medicinskaia genetika». 22(2). 48–51. 2 indexed citations
11.
Kondratyeva, E., Н.В. Петрова, A. V. Polyakov, et al.. (2023). Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR Channel. Genes. 14(9). 1705–1705. 6 indexed citations
12.
Нероев, В. В., Л. А. Катаргина, Ekaterina V. Denisova, et al.. (2023). First results of long-term follow-up of children in Russia after gene therapy for hereditary retinal dystrophies associated with biallelic mutations in the RPE65 gene. Russian Ophthalmological Journal. 16(4). 50–62.
13.
Vasilyeva, Tatyana A., et al.. (2023). Co-Occurrence of Congenital Aniridia Due to Nonsense PAX6 Variant p.(Cys94*) and Chromosome 21 Trisomy in the Same Patient. International Journal of Molecular Sciences. 24(21). 15527–15527.
14.
Зинченко, Р. А., et al.. (2022). Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation). Russian Annals of Ophthalmology. 138(5). 80–80.
15.
Kondratyeva, E., Т. Б. Бухарова, Mikhail Skoblov, et al.. (2021). Health Characteristics of Patients with Cystic Fibrosis whose Genotype Includes a Variant of the Nucleotide Sequence c.3140-16T>A and Functional Analysis of this Variant. Genes. 12(6). 837–837. 9 indexed citations
16.
Петрова, Н.В., et al.. (2021). CYSTIC FIBROSIS: ETIOLOGY, PATHOGENESIS, CLINICAL MANIFESTATIONS, RESULTS OF NEONATAL SCREENING AND GENETIC ASPECTS IN NORTH OSSETIA – ALANIA. PEDIATRIA Journal named after G N SPERANSKY. 100(1). 222–228. 1 indexed citations
17.
18.
Катаргина, Л. А., et al.. (2020). А clinical case of WAGRO syndrome. 15(2). 19–24. 1 indexed citations
19.
Зинченко, Р. А., et al.. (2020). DISABILITY AND MORTALITY RATES OF THE CHILD POPULATION OF THE RUSSIAN FEDERATION IN CASE OF RARE (ORPHAN) DISEASES. PEDIATRIA Journal named after G N SPERANSKY. 99(3). 271–278. 1 indexed citations
20.
Зинченко, Р. А., et al.. (2019). Distribution of the modern Osset surnames. Moscow University Anthropology Bulletin (Vestnik Moskovskogo Universiteta Seria XXIII Antropologia). 86–92.

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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