Н.В. Петрова

604 citations

65 papers · 280 · h-index 9

Impact in

Pulmonary and Respiratory Medicine
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
Sensory Systems
- Hearing, Cochlea, Tinnitus, Genetics

Papers in

Pulmonary and Respiratory Medicine 31
- Cystic Fibrosis Research Advances 29
- Neonatal Respiratory Health Research 16
Genetics 22
- Nutrition, Genetics, and Disease 11
- Digestive system and related health 7
- Genomics and Rare Diseases 4

Co-authors: Р. А. Зинченко (48 shared papers)Andrey V. Marakhonov (24 shared papers)Sergey I. Kutsev (23 shared papers)N. Kashirskaya (17 shared papers)Tatyana A. Vasilyeva (16 shared papers)E. Kondratyeva (14 shared papers)A. Voronkova (13 shared papers)V. Sherman (16 shared papers)
Journals: Journal of Cystic Fibrosis (5 papers)Genes (5 papers)Frontiers in Pediatrics (2 papers)Frontiers in Genetics (2 papers)International Journal of Molecular Sciences (2 papers)
Partner nations: Russia United States South Korea

In The Last Decade

Н.В. Петрова

59 papers receiving 270 citations

Peers

Countries citing papers authored by Н.В. Петрова

Since Specialization

Citations

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

Fields of papers citing papers by Н.В. Петрова

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Н.В. Петрова. 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 Н.В. Петрова. The network helps show where Н.В. Петрова may publish in the future.

Co-authors

The 25 scholars most cited alongside Н.В. Петрова, 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 Н.В. Петрова Line = papers co-authored together Н.В. Петрова 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 65 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients Genes ·Н.В. Петрова, N. Kashirskaya, Tatyana A. Vasilyeva, E. Kondratyeva, E. Zhekaite, A. Voronkova, V. Sherman, В. А. Галкина, Eugeny K. Ginter, Sergey I. Kutsev, Andrey V. Marakhonov, Р. А. Зинченко	2020	27
2	TNF gene polymorphisms in cystic fibrosis patients: contribution to the disease progression Journal of Translational Medicine ·Г. В. Шмарина, Alexander Pukhalsky, Н.В. Петрова, Ekaterina Zakharova, L. Avakian, N. I. Kapranov, Vladimir Alioshkin	2013	21
3	Ethnic Differences in the Frequency of CFTR Gene Mutations in Populations of the European and North Caucasian Part of the Russian Federation Frontiers in Genetics ·Н.В. Петрова, Natalia Balinova, Andrey V. Marakhonov, Tatyana A. Vasilyeva, N. Kashirskaya, В. А. Галкина, E Ginter, Sergey I. Kutsev, Р. А. Зинченко	2021	21
4	High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia Journal of Cystic Fibrosis ·Н.В. Петрова, N. Kashirskaya, Tatyana A. Vasilyeva, E.E. Timkovskaya, A. Voronkova, L. Shabalova, E. Kondratyeva, V. Sherman, О.Г. Новоселова, N. Kapranov, Р. А. Зинченко, E. K. Ginter, А. Х-М. Макаов, Batsheva Kerem	2016	16
5	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
6	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
7	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
8	A Clinical and Molecular Analysis of Branchio‐Oculo‐Facial Syndrome Patients in Russia Revealed New Mutations in TFAP2A Annals of Human Genetics ·T. I. Mescheryakova, Р. А. Зинченко, Tatyana A. Vasilyeva, Andrey V. Marakhonov, S. S. Zhylina, Н.В. Петрова, T. V. Kozhanova, Maxim S. Belenikin, А. Н. Петрин, G. R. Mutovin	2015	10
9	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
10	Vitamin D Status in Russian Children and Adolescents: Contribution of Genetic and Exogenous Factors Frontiers in Pediatrics ·E. Kondratyeva, И. Н. Захарова, Н. А. Ильенкова, Leonid Klimov, Н.В. Петрова, A. Zodbinova, E. Zhekaite, V. Chikunov, Svetlana Dolbnya, A. Voronkova, V. Sherman, Е. В. Лошкова, Y. Melyanovskaya, Roman M. Budzinskiy, Victoria Kuryaninova, Sergey I. Kutsev	2020	8
11	Clinical and genetic characterization of patients with cystic fibrosis and functional assessment of the chloride channel with the pathogenic variant c.831G>A (p.Trp277), described for the first time Gene* ·E. Kondratyeva, Anna Efremovа, Yu. L. Melyanovskaya, Н.В. Петрова, N. Satsuk, N. Bulatenko, Т. Б. Бухарова, A. Zodbinova, V. Sherman, N. Kashirskaya, Р. А. Зинченко, Sergey I. Kutsev, Dmitry Goldshtein	2020	7
12	High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients BMC Genomics ·Н.В. Петрова, N. Kashirskaya, Tatyana A. Vasilyeva, Natalia Balinova, Andrey V. Marakhonov, E. Kondratyeva, E. Zhekaite, A. Voronkova, Sergey I. Kutsev, Р. А. Зинченко	2022	7
13	Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: Identification of three novel alleles Human Mutation ·C. Verlingue, N. Kapranov, Bernard Mercier, E. K. Ginter, Н.В. Петрова, M.‐P. Audrézet, Claude Férec	1995	7
14	Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR Channel Genes ·E. Kondratyeva, Y. Melyanovskaya, Anna Efremovа, Mariya Krasnova, Diana Mokrousova, N. Bulatenko, Н.В. Петрова, A. V. Polyakov, T. Adyan, Valeriia Kovalskaia, Т. Б. Бухарова, Andrey V. Marakhonov, Р. А. Зинченко, E. Zhekaite, Artem Bukhonin, Dmitry Goldshtein	2023	6
15	Clinical course of cystic fibrosis on adult patients carrying "mild" mutations PULMONOLOGIYA ·S. Krasovsky, Н.В. Петрова, A. A. Stepanova, M. Usacheva, Vladimir A. Samoilenko, Е. Л. Амелина, V. Nikonova	2012	5
16	Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population Genes ·Н.В. Петрова, Andrey V. Marakhonov, Natalia Balinova, Anna V. Abrukova, Fedor A. Konovalov, Sergey I. Kutsev, Р. А. Зинченко	2021	5
17	Genetic structure of the Udmurt population Russian Journal of Genetics ·Р. А. Зинченко, Г. И. Ельчинова, Н.В. Петрова, E. V. Osipova, P. Yu. Malyshev, A. V. Polyakov, Ginter Ek	2007	5
18	Epidemiology of Rare Hereditary Diseases in the European Part of Russia: Point and Cumulative Prevalence Frontiers in Genetics ·Р. А. Зинченко, Eugeny K. Ginter, Andrey V. Marakhonov, Н.В. Петрова, В. В. Кадышев, Tatyana P. Vasilyeva, Oksana U. Alexandrova, A. V. Polyakov, Sergey I. Kutsev	2021	4
19	A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region BMC Medical Genomics ·Tatyana A. Vasilyeva, Andrey V. Marakhonov, М.Е. Миньженкова, Ж.Г. Маркова, Н.В. Петрова, Natella V. Sukhanova, K Philipp, Denis V. Pyankov, Ilya Kanivets, С. А. Коростелев, Irina A. Krynskaya, Н.В. Шилова, Sergey I. Kutsev, В. В. Кадышев, Р. А. Зинченко	2020	4
20	Phenotypic features in patients with cystic fibrosis with L138ins (p.Leu138dup) mutation PEDIATRIA Journal named after G N SPERANSKY ·Н.В. Петрова, N. Kashirskaya, Tatyana A. Vasilyeva, A. Voronkova, Elena Ivanovna Kondratieva, V. Sherman, О.Г. Новоселова, S. Krasovskiy, А. V. Chernyak, Е. Л. Амелина, E Ginter, Sergey I. Kutsev, Р. А. Зинченко	2017	4

About Н.В. Петрова

Н.В. Петрова is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Pediatrics, Perinatology and Child Health, Immunology and Emergency Medical Services, having authored 65 papers that have together received 280 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (29 papers), Neonatal Respiratory Health Research (16 papers), Nutrition, Genetics, and Disease (11 papers), Human Health and Disease (8 papers), Digestive system and related health (7 papers), Immunodeficiency and Autoimmune Disorders (7 papers), Pediatric health and respiratory diseases (6 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (147 citations), Sensory Systems (19 citations), Emergency Medical Services (15 citations), Genetics (23 citations) and Neurology (14 citations). Н.В. Петрова has collaborated with scholars based in Russia, United States and South Korea. Frequent co-authors include Р. А. Зинченко, Andrey V. Marakhonov, Sergey I. Kutsev, N. Kashirskaya, Tatyana A. Vasilyeva, E. Kondratyeva, A. Voronkova, V. Sherman, A. V. Polyakov and E. K. Ginter. Their work appears in journals such as Journal of Cystic Fibrosis, Genes, Frontiers in Pediatrics, Frontiers in Genetics and International Journal of Molecular Sciences.

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Н.В. Петрова

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