Viktoriia V Zabnenkova (Viktoriia Zabnenkova, Victoriia V Zabnenkova, Viktoria Zabnenkova, V V Zabnenkova)

Publication Activity (10 Years)

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

Top Topics

Dna Methylation

Top Venues

Journal of clinical immunology

The application of clinical genetics

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

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)
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)
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)
G E Rudenskaya, M S Petukhova, Viktoriia V Zabnenkova, Tatiana B Cherevatova, Oxana P Ryzhkova
[Early-onset familial Alzheimer's disease with spastic paraparesis associated with PSEN1 gene]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 123 (11) (2023)
Kristina Michalchuk, Olga A Shchagina, Alena Chukhrova, Viktoriia V Zabnenkova, Polina Chausova, Nina Ryadninskaya, Dmitry V Vlodavets, Sergei I Kutsev, Alexander Polyakov
Pilot Program of Newborn Screening for 5q Spinal Muscular Atrophy in the Russian Federation. International journal of neonatal screening 9 (2) (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)
Viktoriia V Zabnenkova, Olga A Shchagina, Olga Makienko, Galina Matyushchenko, Oxana P Ryzhkova
Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome. The application of clinical genetics 15 (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)