A. V. Polyakov

4.2k citations

133 papers · 1.0k · h-index 14

Impact in

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

Papers in

Molecular Biology 61
- Muscle Physiology and Disorders 10
- Connexins and lens biology 9
Genetics 30
- Neurogenetic and Muscular Disorders Research 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9

Co-authors: Oleg V. Evgrafov (7 shared papers)Е. Л. Дадали (21 shared papers)V. F. Sitnikov (1 shared paper)А. Н. Петрин (1 shared paper)Irina Mersiyanova (2 shared papers)Р. А. Зинченко (26 shared papers)И. И. Дедов (4 shared papers)Valentina Peterkova (3 shared papers)
Journals: International Journal of Molecular Sciences (6 papers)Frontiers in Genetics (5 papers)Genes (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

116 papers receiving 1.0k 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	345
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	41
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, Alexander Karachunskiy, Oleg Togoev, Andrey Timakov, A. V. Polyakov, Svetlana Tverskaya, Oleg V. Evgrafov, Alexander Roumiantsev	2003	33
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	32
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	31
6	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	30
7	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, (unknown), S.V. Voronin, E. К. Kudryashova, Oleg S. Glotov, A. V. Polyakov	2017	28
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	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	16
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	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
12	Primary ciliary dyskinesia: review of the draft clinical guidelines, 2022 PULMONOLOGIYA ·E. Kondratyeva, С. Н. Авдеев, В. К. Котлуков, 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	14
13	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	14
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	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
16	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
17	Epidemiology of hearing loss in children of the first year of life Russian Bulletin of Otorhinolaryngology ·S S Chibisova, Т Г Маркова, Н. Н. Алексеева, A. A. Yasinskaya, E R Tsygankova, E. A. Bliznetz, A. V. Polyakov, Г А Таварткиладзе	2018	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	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
20	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	10

About A. V. Polyakov

A. V. Polyakov is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Cellular and Molecular Neuroscience and Sensory Systems, having authored 133 papers that have together received 1.0k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (18 papers), Cystic Fibrosis Research Advances (15 papers), Neonatal Respiratory Health Research (12 papers), Genetic Neurodegenerative Diseases (12 papers), Neurogenetic and Muscular Disorders Research (11 papers), Muscle Physiology and Disorders (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers) and Connexins and lens biology (9 papers). The work is most often cited by research in Sensory Systems (133 citations), Neurology (173 citations), Cellular and Molecular Neuroscience (327 citations), Neurology (141 citations) and Genetics (90 citations). A. V. Polyakov has collaborated with scholars based in Russia, United Kingdom and United States. Frequent co-authors include Oleg V. Evgrafov, Е. Л. Дадали, V. F. Sitnikov, А. Н. Петрин, Irina Mersiyanova, Р. А. Зинченко, И. И. Дедов, Valentina Peterkova, Г А Таварткиладзе and О. П. Рыжкова. Their work appears in journals such as International Journal of Molecular Sciences, Frontiers in Genetics, Genes, International Journal of Pediatric Otorhinolaryngology and The Journal of Clinical Endocrinology & Metabolism.

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