A. V. Polyakov

4.1k citations

133 papers · 976 indexed · h-index 14

Impact in

Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 5%
- Neurological diseases and metabolism

Papers in ⓘ

Sensory Systems 18
- Hearing, Cochlea, Tinnitus, Genetics 18
Clinical Biochemistry 9

Co-authors: Е. Л. Дадали (21 shared papers)Oleg V. Evgrafov (7 shared papers)А. Н. Петрин (1 shared paper)V. F. Sitnikov (1 shared paper)Irina Mersiyanova (2 shared papers)Р. А. Зинченко (26 shared papers)Г А Таварткиладзе (13 shared papers)Valentina Peterkova (3 shared papers)
Journals: International Journal of Molecular Sciences (6 papers)Genes (5 papers)Frontiers in Genetics (5 papers)International Journal of Pediatric Otorhinolaryngology (3 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)
Partner nations: Russia United Kingdom United States

In The Last Decade

A. V. Polyakov

115 papers receiving 951 citations

Peers

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-authors

The 25 scholars most cited alongside A. V. Polyakov, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with A. V. Polyakov Line = papers co-authored together A. V. Polyakov links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 133 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene The American Journal of Human Genetics ·Irina Mersiyanova, Alexander V. Perepelov, A. V. Polyakov, V. F. Sitnikov, Е. Л. Дадали, Roman B. Oparin, А. Н. Петрин, Oleg V. Evgrafov	2000	319
2	Comparative cytogenetics of hamsters of the genus <i>Calomyscus</i> Cytogenetic and Genome Research ·Alexander S. Graphodatsky, О.В. Саблина, Marlies Meyer, V.G. Malikov, E.A. Isakova, Vladimir A. Trifonov, A. V. Polyakov, Tamara Lushnikova, Nadezhda V. Vorobieva, Natalia A. Serdyukova, Polina L. Perelman, Pavel M. Borodin, Pavel Benda, Daniel Frynta, L. Leikepová, Pavel Munclinger, Jaroslav Piálek, Jovana Sádlová, Jan Zima	2000	39
3	657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls American Journal of Medical Genetics Part A ·Igor Resnick, Irina Kondratenko, Eugeni Pashanov, Alexey Maschan, А. I. Karachunsky, Oleg Togoev, Andrey Timakov, A. V. Polyakov, Svetlana Tverskaya, Oleg V. Evgrafov, Alexander Roumiantsev	2003	32
4	Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect European Journal of Human Genetics ·E. A. Bliznetz, Svetlana Tverskaya, Р. А. Зинченко, Anna V. Abrukova, Ekaterina N Savaskina, Maxim V Nikulin, A. G. Kirillov, E. K. Ginter, A. V. Polyakov	2009	31
5	A Novel IVS2 −2A>T Splicing Mutation in theGH-1Gene in Familial Isolated Growth Hormone Deficiency Type II in the Spectrum of Other Splicing Mutations in the Russian Population The Journal of Clinical Endocrinology & Metabolism ·О. В. Фофанова, Oleg V. Evgrafov, A. V. Polyakov, А. Б. Полтараус, Valentina Peterkova, И. И. Дедов	2003	29
6	Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions Journal of Human Genetics ·E. A. Bliznetz, M.R. Lalayants, Т Г Маркова, Oleg Balanovsky, Elena Balanovska, R. A. Skhalyakho, Elvira Pocheshkhova, Natalya I. Nikitina, S.V. Voronin, E. К. Kudryashova, Oleg S. Glotov, A. V. Polyakov	2017	27
7	A Potential Rearrangement between CYP19 and TRPM7 Genes on Chromosome 15q21.2 as a Cause of Aromatase Excess Syndrome The Journal of Clinical Endocrinology & Metabolism ·Anatoly Tiulpakov, Natalya Kalintchenko, Tatyana Semitcheva, A. V. Polyakov, И. И. Дедов, P.S. Sverdlova, Г С Колесникова, Valentina Peterkova, П. М. Рубцов	2005	23
8	Changes in the connexin 26 gene (GJB2) in Russian patients with hearing loss: Results of long-term molecular diagnostics of hereditary nonsyndromic hearing loss Russian Journal of Genetics ·E. A. Bliznetz, В. А. Галкина, G. N. Matyushchenko, A. G. Kisina, Т Г Маркова, A. V. Polyakov	2012	18
9	Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy International Journal of Molecular Sciences ·E. Kondratyeva, Anna Efremovа, Y. Melyanovskaya, A. Voronkova, A. V. Polyakov, N. Bulatenko, T. Adyan, Viktoriya Sherman, Valeriia Kovalskaia, Н.В. Петрова, M. Starinova, Т. Б. Бухарова, Sergey I. Kutsev, Dmitry Goldshtein	2022	15
10	Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia Prenatal Diagnosis ·В. С. Баранов, V. N. Gorbunova, Olga Malysheva, Olga V. Artemyeva, T. K. Kascheeva, Oleg V. Evgrafov, A. V. Polyakov, В. М. Лебедев, T. V. Kuznetzova, S. N. Shlykova, А. В. Михайлов, V. G. Vakharlovsky	1993	15
11	HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients Molecular Biology Reports ·Olga Shchagina, (unknown), Aysylu Murtazina, G. N. Rudenskaya, С. С. Никитин, Е. Л. Дадали, A. V. Polyakov	2019	15
12	Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus BMC Medical Genetics ·Н.В. Петрова, N. Kashirskaya, D. Kh. Saydaeva, A. V. Polyakov, T. Adyan, О. И. Симонова, Y. Gorinova, E. Kondratyeva, V. Sherman, О.Г. Новоселова, Tatyana A. Vasilyeva, Andrey V. Marakhonov, Milan Maçek, E Ginter, Р. А. Зинченко	2019	13
13	Prevalences of hereditary diseases in different populations of Russia Russian Journal of Genetics ·Р. А. Зинченко, Г. И. Ельчинова, Н. В. Барышникова, A. V. Polyakov, Ginter Ek	2007	13
14	Mutation p.E92K is the primary cause of cystic fibrosis in Chuvashes Russian Journal of Genetics ·Анна Степанова, Anna V. Abrukova, Ekaterina N Savaskina, A. V. Polyakov	2012	13
15	Primary ciliary dyskinesia: review of the draft clinical guidelines, 2022 PULMONOLOGIYA ·E. Kondratyeva, С. Н. Авдеев, Yu. L. Mizernitskiy, A. V. Polyakov, M.Y. Chernukha, О. В. Кондратенко, Leyla S. Namazova-Baranova, Еlena A. Vishneva, Liliya R. Selimzyanova, О. И. Симонова, Т. E. Gembitskaya, Е. Е. Брагина, Svetlana Rachina, А.Б. Малахов, D. P. Polyakov, Н. Д. Одинаева, Sergey I. Kutsev	2022	11
16	Molecular genetic diagnosis of Stargardt disease Russian Annals of Ophthalmology ·Н Л Шеремет, Н В Жоржоладзе, И А Ронзина, И.Г. Грушкэ, С. В. Курбатов, А. Л. Чухрова, А. Н. Логинова, P O Shcherbakova, А. С. Танас, A. V. Polyakov, V. V. Strelnikov	2017	11
17	Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population International Journal of Pediatric Otorhinolaryngology ·Т Г Маркова, Н. Н. Алексеева, О. Л. Миронович, Н. М. Галеева, M.R. Lalayants, E. A. Bliznetz, S S Chibisova, A. V. Polyakov, Г А Таварткиладзе	2020	11
18	Epidemiology of Hereditary Diseases in the Karachay-Cherkess Republic International Journal of Molecular Sciences ·Р. А. Зинченко, А. Х. Макаов, Andrey V. Marakhonov, В. А. Галкина, В. В. Кадышев, Г. И. Ельчинова, Е. Л. Дадали, Л. К. Михайлова, Н.В. Петрова, Н. Е. Петрина, Tatyana A. Vasilyeva, П. Гундорова, A. V. Polyakov, OKSANA YU . ALEXANDROVA, Sergey I. Kutsev, E. K. Ginter	2020	11
19	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 ·E. Kondratyeva, Т. Б. Бухарова, Anna Efremovа, Y. Melyanovskaya, N. Bulatenko, Kseniya Davydenko, Alexandra Filatova, Mikhail Skoblov, S. Krasovsky, Н.В. Петрова, A. V. Polyakov, T. Adyan, E. Amelina, V. Shadrina, E. Zhekaite, Aysa Zodbinova, А. V. Chernyak, Р. А. Зинченко, Sergey I. Kutsev, Dmitry Goldshtein	2021	9
20	Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del] Current Issues in Molecular Biology ·E. Kondratyeva, N. Bulatenko, Y. Melyanovskaya, Anna Efremovа, E. Zhekaite, Viktoriya Sherman, A. Voronkova, I. Asherova, A. V. Polyakov, T. Adyan, Valeriia Kovalskaia, Т. Б. Бухарова, Dmitry Goldshtein, Sergey I. Kutsev	2022	9

About A. V. Polyakov

A. V. Polyakov is a scholar working on Sensory Systems, Clinical Biochemistry, Neurology, Genetics and Genetics, having authored 133 papers that have together received 976 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (18 papers), Cystic Fibrosis Research Advances (15 papers), Genetic Neurodegenerative Diseases (13 papers), Neonatal Respiratory Health Research (12 papers), Muscle Physiology and Disorders (12 papers), Neurogenetic and Muscular Disorders Research (11 papers), Hereditary Neurological Disorders (9 papers) and Connexins and lens biology (9 papers). The work is most often cited by research in Sensory Systems (126 citations), Neurology (175 citations), Cellular and Molecular Neuroscience (312 citations), Neurology (146 citations) and Genetics (92 citations). A. V. Polyakov has collaborated with scholars based in Russia, United Kingdom and United States. Frequent co-authors include Е. Л. Дадали, Oleg V. Evgrafov, А. Н. Петрин, V. F. Sitnikov, Irina Mersiyanova, Р. А. Зинченко, Г А Таварткиладзе, Valentina Peterkova, И. И. Дедов and Анна Степанова. Their work appears in journals such as International Journal of Molecular Sciences, Genes, Frontiers in Genetics, International Journal of Pediatric Otorhinolaryngology and The Journal of Clinical Endocrinology & Metabolism.

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