A. V. Polyakov

4.1k total citations
133 papers, 976 citations indexed

About

A. V. Polyakov is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, A. V. Polyakov has authored 133 papers receiving a total of 976 indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 30 papers in Genetics and 20 papers in Pulmonary and Respiratory Medicine. Recurrent topics in A. V. Polyakov's work include Hearing, Cochlea, Tinnitus, Genetics (18 papers), Cystic Fibrosis Research Advances (15 papers) and Genetic Neurodegenerative Diseases (13 papers). A. V. Polyakov is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (18 papers), Cystic Fibrosis Research Advances (15 papers) and Genetic Neurodegenerative Diseases (13 papers). A. V. Polyakov collaborates with scholars based in Russia, United Kingdom and United States. A. V. Polyakov's co-authors include Е. Л. Дадали, Oleg V. Evgrafov, V. F. Sitnikov, А. Н. Петрин, Irina Mersiyanova, Р. А. Зинченко, И. И. Дедов, Г А Таварткиладзе, Valentina Peterkova and Анна Степанова and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and International Journal of Molecular Sciences.

In The Last Decade

A. V. Polyakov

115 papers receiving 951 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. V. Polyakov Russia 14 415 312 188 175 146 133 976
Horia Stanescu United Kingdom 18 536 1.3× 251 0.8× 185 1.0× 71 0.4× 90 0.6× 42 1.3k
Félix Prieto Spain 16 369 0.9× 223 0.7× 151 0.8× 148 0.8× 97 0.7× 40 869
Thalia Antoniadi Greece 16 327 0.8× 217 0.7× 155 0.8× 145 0.8× 61 0.4× 28 850
Güney Bademci United States 19 582 1.4× 91 0.3× 331 1.8× 166 0.9× 155 1.1× 63 1.1k
Guntram Borck Germany 27 876 2.1× 133 0.4× 681 3.6× 136 0.8× 114 0.8× 65 1.7k
Emanuela Leonardi Italy 20 461 1.1× 111 0.4× 125 0.7× 106 0.6× 63 0.4× 38 850
Sohyun Ahn United States 12 1.1k 2.6× 329 1.1× 241 1.3× 98 0.6× 100 0.7× 17 1.6k
Guy A. Rouleau Canada 17 433 1.0× 146 0.5× 139 0.7× 89 0.5× 278 1.9× 36 835
Thomas Van Winkle United States 13 389 0.9× 263 0.8× 60 0.3× 174 1.0× 286 2.0× 16 1.1k
JoAnn Bergoffen United States 11 634 1.5× 577 1.8× 221 1.2× 148 0.8× 294 2.0× 13 1.2k

Countries citing papers authored by A. V. Polyakov

Since Specialization
Citations

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

Fields of papers citing papers by A. V. Polyakov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. V. Polyakov. 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 A. V. Polyakov. The network helps show where A. V. Polyakov may publish in the future.

Co-authorship network of co-authors of A. V. Polyakov

This figure shows the co-authorship network connecting the top 25 collaborators of A. V. Polyakov. A scholar is included among the top collaborators of A. V. Polyakov 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 A. V. Polyakov. A. V. Polyakov 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.
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
2.
Степанова, Анна, et al.. (2024). Frequent Genetic Variants of Autosomal Recessive Nonsyndromic Forms of Inherited Retinal Diseases in the Russian Federation. Russian Journal of Genetics. 60(4). 503–515. 1 indexed citations
3.
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
4.
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.
5.
Alekseeva, Ekaterina A., V. V. Strelnikov, A. V. Polyakov, et al.. (2023). Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population. International Journal of Molecular Sciences. 24(22). 16231–16231. 1 indexed citations
6.
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.
7.
Kondratyeva, E., et al.. (2022). Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del]. Current Issues in Molecular Biology. 44(10). 5126–5138. 9 indexed citations
8.
Kondratyeva, E., A. V. Polyakov, Н.В. Петрова, et al.. (2022). Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy. International Journal of Molecular Sciences. 23(18). 10377–10377. 15 indexed citations
9.
Kondratyeva, E., С. Н. Авдеев, A. V. Polyakov, et al.. (2022). Primary ciliary dyskinesia: review of the draft clinical guidelines, 2022. PULMONOLOGIYA. 32(4). 517–538. 11 indexed citations
10.
Рыжкова, О. П., et al.. (2022). Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss. Journal of Personalized Medicine. 12(11). 1843–1843. 2 indexed citations
11.
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
12.
Дадали, Е. Л., et al.. (2021). A Two-Year Clinical Description of a Patient with a Rare Type of Low-GGT Cholestasis Caused by a Novel Variant of USP53. Genes. 12(10). 1618–1618. 6 indexed citations
13.
Рыжкова, О. П., et al.. (2020). Spastic paraplegias types 11 and 15. SHILAP Revista de lepidopterología. 14(4). 29–38. 1 indexed citations
14.
Polyakov, A. V., et al.. (2020). Genetic examination of children with hearing impairment in the astrakhan region. Russian otorhinolaryngology. 19(5). 44–50. 1 indexed citations
15.
Дадали, Е. Л., et al.. (2020). Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia. SHILAP Revista de lepidopterología. 10(2). 39–45. 1 indexed citations
16.
Роживанов, Р. В., et al.. (2018). ANDROLOGY EXAMINATION OF PATIENTS WITH PANCREATIC-SUFFICIENT AND PANCREATIC-INSUFFICIENT CYSTIC FIBROSIS. Andrology and Genital Surgery. 19(2). 31–39. 1 indexed citations
17.
Петрова, Н.В., N. Kashirskaya, Sergey I. Kutsev, et al.. (2018). Cystic fibrosis phenotype with the complex allele s466x-r1070q in Russian Federation Elena I. Kondrat'eva1. PULMONOLOGIYA. 27(6). 695–703. 2 indexed citations
18.
19.
Amelina, E., et al.. (2013). The impact of genotype on clinical course of cystic fibrosis (CF) in adult patients. European Respiratory Journal. 42(Suppl 57). P1179–P1179. 2 indexed citations
20.
Agulnik, Alexander I., et al.. (1990). The tctN mutation, which causes taillessness in mice heterozygous for the T gene.. 26(8). 1462–1468. 1 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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