Valeriia A Kovalskaia (Valeriia Kovalskaia)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 15

Top Topics

Intellectual Disability

Children With Cerebral Palsy

Top Venues

International journal of molecular sciences

Current issues in molecular biology

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

Publications

Valeriia A Kovalskaia, Anastasiia L Kungurtseva, Fatima M Bostanova, Petr Andreevich Vasiluev, Vyacheslav Y Tabakov, Mariia D Orlova, Inna S Povolotskaya, Olga G Novoselova, Roman A Bikanov, Mariia A Akhyamova, Yulia V Tikhonovich, Anastasiia V Popovich, Alisa V Vitebskaya, Elena L Dadali, Oxana P Ryzhkova
The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation. Genes 15 (2) (2024)
Valeriia A Kovalskaia, Anastasiia L Kungurtseva, Fatima M Bostanova, Petr Andreevich Vasiluev, Vyacheslav Y Tabakov, Mariia D Orlova, Inna S Povolotskaya, Olga G Novoselova, Roman A Bikanov, Mariia A Akhyamova, Yulia V Tikhonovich, Anastasiia V Popovich, Alisa V Vitebskaya, Elena L Dadali, Oxana P Ryzhkova
The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation. Genes 15 (2) (2024)
Valeriia A Kovalskaia, Anastasiia L Kungurtseva, Fatima M Bostanova, Petr Andreevich Vasiluev, Vyacheslav Y Tabakov, Mariia D Orlova, Inna S Povolotskaya, Olga G Novoselova, Roman A Bikanov, Mariia A Akhyamova, Yulia V Tikhonovich, Anastasiia V Popovich, Alisa V Vitebskaya, Elena L Dadali, Oxana P Ryzhkova
The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation. Genes 15 (2) (2024)
Valeriia A Kovalskaia, Anastasiia L Kungurtseva, Fatima M Bostanova, Petr Andreevich Vasiluev, Vyacheslav Y Tabakov, Mariia D Orlova, Inna S Povolotskaya, Olga G Novoselova, Roman A Bikanov, Mariia A Akhyamova, Yulia V Tikhonovich, Anastasiia V Popovich, Alisa V Vitebskaya, Elena L Dadali, Oxana P Ryzhkova
The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation. Genes 15 (2) (2024)
Polina Chausova, Aysylu F Murtazina, Anna Stepanova, Artem O Borovikov, Valeriia A Kovalskaia, Nina Ryadninskaya, Alena Chukhrova, Oxana P Ryzhkova, Aleksander Poliakov
X-Linked Myotubular Myopathy in a Female Patient with a Pathogenic Variant in the MTM1 Gene. International journal of molecular sciences 24 (9) (2023)
Polina Chausova, Aysylu F Murtazina, Anna Stepanova, Artem O Borovikov, Valeriia A Kovalskaia, Nina Ryadninskaya, Alena Chukhrova, Oxana P Ryzhkova, Aleksander Poliakov
X-Linked Myotubular Myopathy in a Female Patient with a Pathogenic Variant in the MTM1 Gene. International journal of molecular sciences 24 (9) (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)
Polina Chausova, Aysylu F Murtazina, Anna Stepanova, Artem O Borovikov, Valeriia A Kovalskaia, Nina Ryadninskaya, Alena Chukhrova, Oxana P Ryzhkova, Aleksander Poliakov
X-Linked Myotubular Myopathy in a Female Patient with a Pathogenic Variant in the MTM1 Gene. International journal of molecular sciences 24 (9) (2023)
Olga Mironovich, Valeriia A Kovalskaia, Peter A Sparber, Inna Sharkova, Irina Mishina, Vera Kuznetsova, Oxana P Ryzhkova
TRA2B Gene Splice Variant Linked to Seizures and Neurodevelopmental Delay: A Second Case Study. International journal of molecular sciences 24 (21) (2023)
Valeriia A Kovalskaia, Viktoriia V Zabnenkova, Marina S Petukhova, Zhanna G Markova, Vyacheslav Yu Tabakov, Oxana P Ryzhkova
Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia. Genes 13 (12) (2022)
Valeriia A Kovalskaia, Viktoriia V Zabnenkova, Marina S Petukhova, Zhanna G Markova, Vyacheslav Yu Tabakov, Oxana P Ryzhkova
Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia. Genes 13 (12) (2022)
Elena I Kondratyeva, Anna Efremova, Yuliya Melyanovskaya, Anna Voronkova, Alexander Polyakov, Nataliya Bulatenko, Tagui Adyan, Victoria D Sherman, Valeriia A Kovalskaia, Nika Petrova, Marina Starinova, Tatiana Borisovna Bukharova, Sergei Kutsev, Dmitry Goldshtein
Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy. International journal of molecular sciences 23 (18) (2022)
Elena Kondratyeva, Nataliya Bulatenko, Yuliya Melyanovskaya, Anna Efremova, Elena Zhekaite, Victoria D Sherman, Anna Voronkova, Irina Asherova, Alexander Polyakov, Tagui Adyan, Valeriia A Kovalskaia, Tatiana Borisovna Bukharova, Dmitry Goldshtein, Sergey Kutsev
Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del]. Current issues in molecular biology 44 (10) (2022)
Valeriia A Kovalskaia, Viktoriia V Zabnenkova, Marina S Petukhova, Zhanna G Markova, Vyacheslav Yu Tabakov, Oxana P Ryzhkova
Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia. Genes 13 (12) (2022)
Valeriia A Kovalskaia, Viktoriia V Zabnenkova, Marina S Petukhova, Zhanna G Markova, Vyacheslav Yu Tabakov, Oxana P Ryzhkova
Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia. Genes 13 (12) (2022)