Rena A Zinchenko (Rena Zinchenko, R A Zinchenko)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 41

Top Topics

Cystic Fibrosis

Top Venues

International journal of molecular sciences

Current issues in molecular biology

Vestnik oftalmologii

This page only lists publications with an associated author ORCID identifier.

Publications

Andrey A Marakhonov, Irina Yu Efimova, Anna A Mukhina, Rena A Zinchenko, Natalia V Balinova, Yulia Rodina, Dmitriy Pershin, Oxana P Ryzhkova, Anna A Orlova, Viktoriia V Zabnenkova, Tatiana B Cherevatova, Tatiana S Beskorovainaya, Olga A Shchagina, Alexander V Polyakov, Zhanna G Markova, Marina E Minzhenkova, Nadezhda V Shilova, Sergey S Larin, Maryam B Khadzhieva, Ekaterina S Dudina, Ekaterina V Kalinina, Dzhaina A Mudaeva, Djamila H Saydaeva, Svetlana A Matulevich, Elena Yu Belyashova, Grigoriy I Yakubovskiy, Inna S Tebieva, Yulia V Gabisova, Nataliya A Irinina, Liya R Nurgalieva, Elena V Saifullina, Tatiana I Belyaeva, Olga S Romanova, Sergey V Voronin, Anna Shcherbina, Sergey I Kutsev
Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns. Journal of clinical immunology 44 (4) (2024)
Inna S Tebieva, Polina V Mishakova, Yulia V Gabisova, Alana V Khokhova, Tamara G Kaloeva, Andrey A Marakhonov, Olga A Shchagina, Alexander V Polyakov, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
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) (2024)
Andrey A Marakhonov, Irina Yu Efimova, Anna A Mukhina, Rena A Zinchenko, Natalia V Balinova, Yulia Rodina, Dmitriy Pershin, Oxana P Ryzhkova, Anna A Orlova, Viktoriia V Zabnenkova, Tatiana B Cherevatova, Tatiana S Beskorovainaya, Olga A Shchagina, Alexander V Polyakov, Zhanna G Markova, Marina E Minzhenkova, Nadezhda V Shilova, Sergey S Larin, Maryam B Khadzhieva, Ekaterina S Dudina, Ekaterina V Kalinina, Dzhaina A Mudaeva, Djamila H Saydaeva, Svetlana A Matulevich, Elena Yu Belyashova, Grigoriy I Yakubovskiy, Inna S Tebieva, Yulia V Gabisova, Nataliya A Irinina, Liya R Nurgalieva, Elena V Saifullina, Tatiana I Belyaeva, Olga S Romanova, Sergey V Voronin, Anna Shcherbina, Sergey I Kutsev
Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns. Journal of clinical immunology 44 (4) (2024)
Anna Efremova, Nataliya Y Kashirskaya, Stanislav Krasovskiy, Yuliya Melyanovskaya, Maria Krasnova, Diana Mokrousova, Nataliya Bulatenko, Elena I Kondratyeva, Oleg Makhnach, Tatiana Borisovna Bukharova, Rena A Zinchenko, Sergey Kutsev, Dmitry Goldshtein
Comprehensive Assessment of CFTR Modulators' Therapeutic Efficiency for N1303K Variant. International journal of molecular sciences 25 (5) (2024)
Inna S Tebieva, Polina V Mishakova, Yulia V Gabisova, Alana V Khokhova, Tamara G Kaloeva, Andrey A Marakhonov, Olga A Shchagina, Alexander V Polyakov, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
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) (2024)
Sofya A Ionova, Aysylu F Murtazina, Andrey A Marakhonov, Olga A Shchagina, Nina V Ryadninskaya, Inna S Tebieva, Vitaly V Kadyshev, Artem O Borovikov, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
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) (2024)
Inna S Tebieva, Polina V Mishakova, Yulia V Gabisova, Alana V Khokhova, Tamara G Kaloeva, Andrey A Marakhonov, Olga A Shchagina, Alexander V Polyakov, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
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) (2024)
Anna Efremova, Nataliya Y Kashirskaya, Stanislav Krasovskiy, Yuliya Melyanovskaya, Maria Krasnova, Diana Mokrousova, Nataliya Bulatenko, Elena I Kondratyeva, Oleg Makhnach, Tatiana Borisovna Bukharova, Rena A Zinchenko, Sergey Kutsev, Dmitry Goldshtein
Comprehensive Assessment of CFTR Modulators' Therapeutic Efficiency for N1303K Variant. International journal of molecular sciences 25 (5) (2024)
Anna Efremova, Nataliya Y Kashirskaya, Stanislav Krasovskiy, Yuliya Melyanovskaya, Maria Krasnova, Diana Mokrousova, Nataliya Bulatenko, Elena I Kondratyeva, Oleg Makhnach, Tatiana Borisovna Bukharova, Rena A Zinchenko, Sergey Kutsev, Dmitry Goldshtein
Comprehensive Assessment of CFTR Modulators' Therapeutic Efficiency for N1303K Variant. International journal of molecular sciences 25 (5) (2024)
Andrey A Marakhonov, Irina Yu Efimova, Anna A Mukhina, Rena A Zinchenko, Natalia V Balinova, Yulia Rodina, Dmitriy Pershin, Oxana P Ryzhkova, Anna A Orlova, Viktoriia V Zabnenkova, Tatiana B Cherevatova, Tatiana S Beskorovainaya, Olga A Shchagina, Alexander V Polyakov, Zhanna G Markova, Marina E Minzhenkova, Nadezhda V Shilova, Sergey S Larin, Maryam B Khadzhieva, Ekaterina S Dudina, Ekaterina V Kalinina, Dzhaina A Mudaeva, Djamila H Saydaeva, Svetlana A Matulevich, Elena Yu Belyashova, Grigoriy I Yakubovskiy, Inna S Tebieva, Yulia V Gabisova, Nataliya A Irinina, Liya R Nurgalieva, Elena V Saifullina, Tatiana I Belyaeva, Olga S Romanova, Sergey V Voronin, Anna Shcherbina, Sergey I Kutsev
Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns. Journal of clinical immunology 44 (4) (2024)
Tatyana A Vasilyeva, Natella V Sukhanova, Andrey A Marakhonov, Natalia Yu Kuzina, Nadezhda V Shilova, Vitaly V Kadyshev, Sergey I Kutsev, Rena A Zinchenko
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) (2023)
Tatyana A Vasilyeva, Natella V Sukhanova, Olga V Khalanskaya, Andrey A Marakhonov, Nikolai S Prokhorov, Vitaly V Kadyshev, Nikolay A Skryabin, Sergey I Kutsev, Rena A Zinchenko
An Unusual Presentation of Novel Missense Variant in PAX6 Gene: NM_000280.4:c.341A>G, p.(Asn114Ser). Current issues in molecular biology 46 (1) (2023)
Nika Petrova, Inna Tebieva, Vitaly Kadyshev, Zalina Getoeva, Natalia Balinova, Andrey A Marakhonov, Tatyana Vasilyeva, Eugeny K Ginter, Sergey Kutsev, Rena A Zinchenko
Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania. PeerJ 11 (2023)
Tatyana A Vasilyeva, Natella V Sukhanova, Olga V Khalanskaya, Andrey A Marakhonov, Nikolai S Prokhorov, Vitaly V Kadyshev, Nikolay A Skryabin, Sergey I Kutsev, Rena A Zinchenko
An Unusual Presentation of Novel Missense Variant in PAX6 Gene: NM_000280.4:c.341A>G, p.(Asn114Ser). Current issues in molecular biology 46 (1) (2023)
Nika Petrova, Inna Tebieva, Vitaly Kadyshev, Zalina Getoeva, Natalia Balinova, Andrey A Marakhonov, Tatyana Vasilyeva, Eugeny K Ginter, Sergey Kutsev, Rena A Zinchenko
Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania. PeerJ 11 (2023)
Andrey A Marakhonov, Tatyana A Vasilyeva, Marina E Minzhenkova, Natella V Sukhanova, Peter A Sparber, Natalya A Andreeva, Margarita V Teleshova, Fatima K-M Baybagisova, Nadezhda V Shilova, Sergey I Kutsev, Rena A Zinchenko
Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome. International journal of molecular sciences 24 (23) (2023)
Tatyana A Vasilyeva, Andrey A Marakhonov, Inna S Tebieva, Vitaly V Kadyshev, Artem O Borovikov, Zhanna G Markova, Alyona L Chukhrova, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report. International journal of molecular sciences 24 (5) (2023)
Vitaly V Kadyshev, Ekaterina A Alekseeva, Vladimir V Strelnikov, Anna A Stepanova, Alexander V Polyakov, Andrey A Marakhonov, Sergey I Kutsev, Rena A Zinchenko
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) (2023)
Irina Khidiyatova, Indira Khidiyatova, Rena A Zinchenko, Andrey A Marakhonov, Alexandra S Karunas, Svetlana Avkhadeeva, Marat Aznzbaev, Elza K Khusnutdinova
Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga-Ural Region. Current issues in molecular biology 45 (6) (2023)
T A Vasilyeva, Vitaly V Kadyshev, Andrey A Marakhonov, Ilya V Kanivets, S A Korostelev, P A Koshkin, Denis V Pyankov, N V Petrova, Sergey I Kutsev, Rena A Zinchenko
[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy]. Vestnik oftalmologii 139 (1) (2023)
Irina Khidiyatova, Indira Khidiyatova, Rena A Zinchenko, Andrey A Marakhonov, Alexandra S Karunas, Svetlana Avkhadeeva, Marat Aznzbaev, Elza K Khusnutdinova
Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga-Ural Region. Current issues in molecular biology 45 (6) (2023)
Elena I Kondratyeva, Yuliya Melyanovskaya, Anna Efremova, Mariya Krasnova, Diana Mokrousova, Nataliya Bulatenko, Nika Petrova, Alexander Polyakov, Tagui Adyan, Valeriia A Kovalskaia, Tatiana Borisovna Bukharova, Andrey A Marakhonov, Rena A Zinchenko, Elena Zhekaite, Artem Buhonin, Dmitry Goldshtein
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) (2023)
Elena I Kondratyeva, Yuliya Melyanovskaya, Nataliya Bulatenko, Ksenia Davydenko, Alexandra Filatova, Anna Efremova, Mikhail Yurevich Skoblov, Tatiana Borisovna Bukharova, Victoria D Sherman, A Yu Voronkova, Elena Zhekaite, Stanislav Krasovskiy, Elena Amelina, Nika Petrova, Alexander Polyakov, Tagui Adyan, Marina Starinova, Maria Krasnova, Andrey Vyacheslavovich Vasilyev, Oleg Makhnach, Rena A Zinchenko, Sergey Kutsev, Yasemin Gokdemir, Bülent Taner Karadağ, Dmitry Goldshtein
Clinical and Functional Characteristics of the E92K CFTR Gene Variant in the Russian and Turkish Population of People with Cystic Fibrosis. International journal of molecular sciences 24 (7) (2023)
Tatyana A Vasilyeva, Andrey A Marakhonov, Inna S Tebieva, Vitaly V Kadyshev, Artem O Borovikov, Zhanna G Markova, Alyona L Chukhrova, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report. International journal of molecular sciences 24 (5) (2023)
Tatyana A Vasilyeva, Andrey A Marakhonov, Anna A Voskresenskaya, Vitaly V Kadyshev, Natella V Sukhanova, Marina E Minzhenkova, Nadezhda V Shilova, Alla A Latyshova, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
Epidemiology of PAX6 Gene Pathogenic Variants and Expected Prevalence of PAX6 -Associated Congenital Aniridia across the Russian Federation: A Nationwide Study. Genes 14 (11) (2023)
Irina Khidiyatova, Indira Khidiyatova, Rena A Zinchenko, Andrey A Marakhonov, Alexandra S Karunas, Svetlana Avkhadeeva, Marat Aznzbaev, Elza K Khusnutdinova
Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga-Ural Region. Current issues in molecular biology 45 (6) (2023)
Tatyana A Vasilyeva, Andrey A Marakhonov, Inna S Tebieva, Vitaly V Kadyshev, Artem O Borovikov, Zhanna G Markova, Alyona L Chukhrova, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report. International journal of molecular sciences 24 (5) (2023)
Tatyana A Vasilyeva, Andrey A Marakhonov, Sergey I Kutsev, Rena A Zinchenko
Relative Frequencies of PAX6 Mutational Events in a Russian Cohort of Aniridia Patients in Comparison with the World's Population and the Human Genome. International journal of molecular sciences 23 (12) (2022)
I V Zolnikova, S V Milash, Rena A Zinchenko, Alexander V Polyakov, Anna A Stepanova, A B Cherniak, A A Sianosyan, I V Egorova, Vitaly V Kadyshev
[Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)]. Vestnik oftalmologii 138 (5) (2022)
Sofya A Ionova, Aysylu F Murtazina, Inna S Tebieva, Zalina K Getoeva, Elena L Dadali, Polina A Chausova, Olga A Shchagina, Andrey A Marakhonov, Sergey I Kutsev, Rena A Zinchenko
The Presentation of Two Unrelated Clinical Cases from the Republic of North Ossetia-Alania with the Same Previously Undescribed Variant in the COL6A2 Gene. International journal of molecular sciences 23 (20) (2022)
Olga Levchenko, Elena Dadali, Ludmila Bessonova, Nina Demina, Galina Rudenskaya, Galina Matyushchenko, Tatiana Vladimirovna Markova, Inga Anisimova, Natalia Semenova, Olga A Shchagina, Oxana Ryzhkova, Rena A Zinchenko, Varvara Galkina, Victoria Voinova, Sabina Nagieva, Alexander Lavrov
Complex Diagnostics of Non-Specific Intellectual Developmental Disorder. International journal of molecular sciences 23 (14) (2022)
A N Zhuravleva, A M Satybaldyev, Rena A Zinchenko, M O Kirillova, Vitaly V Kadyshev
[Analysis of associations of undifferentiated connective tissue dysplasia with the development of primary open-angle glaucoma. Clinical and genetic aspects]. Vestnik oftalmologii 137 (6) (2021)
I V Zolnikova, Vitaly V Kadyshev, Andrey A Marakhonov, Rena A Zinchenko, A B Cherniak, S V Milash, L V Kogoleva, Yu A Bobrovskaya, N S Kokoeva, I V Egorova, S Yu Rogova
[Fundus albipunctatus with mutations in the RDH5 gene (clinical case)]. Vestnik oftalmologii 137 (1) (2021)
Nika V Petrova, Andrey A Marakhonov, Natalia V Balinova, Anna V Abrukova, Fedor A Konovalov, Sergey I Kutsev, Rena A Zinchenko
Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population. Genes 12 (6) (2021)
Elena I Kondratyeva, Tatiana Borisovna Bukharova, Anna Efremova, Yuliya Melyanovskaya, Natalia Bulatenko, Ksenia Davydenko, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Stanislav Krasovsky, Nika Petrova, Alexander Polyakov, Tagui Adyan, Elena Amelina, Vera Shadrina, Elena Zhekaite, Aysa Zodbinova, Alexander Chernyak, Rena A Zinchenko, Sergei Kutsev, Dmitry Goldshtein
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) (2021)
Andrey A Marakhonov, Magdalena Přechová, Fedor A Konovalov, Alexandra Yu Filatova, Maria A Zamkova, Ilya V Kanivets, Vladimir G Solonichenko, Natalia A Semenova, Rena A Zinchenko, Richard Treisman, Mikhail Yurevich Skoblov
Mutation in PHACTR1 associated with multifocal epilepsy with infantile spasms and hypsarrhythmia. Clinical genetics 99 (5) (2021)
N E Petrina, Andrey A Marakhonov, Rena A Zinchenko
[Presentation of a rare case of hereditary hearing loss with X-linked recessive inheritance associated with the POU3F4 gene]. Vestnik otorinolaringologii 85 (4) (2020)
Nika V Petrova, Nataliya Y Kashirskaya, Stanislav A Krasovskiy, Elena L Amelina, Elena I Kondratyeva, Andrey A Marakhonov, Tatyana A Vasilyeva, Anna Y Voronkova, Victoria D Sherman, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients. Genes 11 (10) (2020)
Tatyana A Vasilyeva, Andrey A Marakhonov, Natella V Sukhanova, Sergey I Kutsev, Rena A Zinchenko
Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome. Genes 11 (7) (2020)
Nika V Petrova, Nataliya Y Kashirskaya, Tatyana A Vasilyeva, Elena I Kondratyeva, Elena K Zhekaite, Anna Y Voronkova, Victoria D Sherman, Varvara A Galkina, Eugeny K Ginter, Sergey I Kutsev, Andrey A Marakhonov, Rena A Zinchenko
Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients. Genes 11 (5) (2020)
Polina Gundorova, Rena A Zinchenko, Irina A Kuznetsova, Elena A Bliznetz, Anna A Stepanova, Aleksander V Polyakov
Molecular-genetic causes for the high frequency of phenylketonuria in the population from the North Caucasus. PloS one 13 (8) (2018)