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Works (16)

Clinical and genetic characteristics of patients with MN1 gene dysfunction after the two clinical case reports

Pediatria. Journal named after G.N. Speransky
2025-02-28 | Journal article
Contributors: Zh.G. Markova; A.S. Kuchina; L.A. Bessonova; V.V. Zabnenkova; S.V. Voronin; N.V. Shilova
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Late verification of primary ciliary dyskinesia and new diagnostic possibilities

PULMONOLOGIYA
2024-12-12 | Journal article
Contributors: E. I. Kondratyeva; T. A. Kyian; E. E. Bragina; A. G. Demchenko; M. V. Tarasov; S. A. Krasovskiy; V. V. Zabnenkova; A. A. Orlova; G. A. Li; O. P. Ryzhkova
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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
2024-05 | Journal article
Contributors: Andrey V. Marakhonov; Irina Yu. Efimova; Anna A. Mukhina; Rena A. Zinchenko; Natalya V. Balinova; Yulia Rodina; Dmitry Pershin; Oxana P. Ryzhkova; Anna A. Orlova; Viktoriia V. Zabnenkova et al.
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Special clinical manifestations and genetic characteristics of schaaf–Yang syndrome in Russian patients

Neuromuscular Diseases
2024-03-01 | Journal article
Contributors: E. L. Dadali; T. V. Markova; F. M. Bostanova; A. S. Kuchina; L. A. Bessonova; E. A. Melnik; V. V. Zabnenkova; O. P. Ryzhkova; O. E. Agranovich
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Crossref

Early-onset familial Alzheimer’s disease with spastic paraparesis associated with PSEN1 gene

Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova
2023 | Journal article
Contributors: G.E. Rudenskaya; M.S. Petukhova; V.V. Zabnenkova; T.B. Cherevatova; O.P. Ryzhkova
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Pilot Program of Newborn Screening for 5q Spinal Muscular Atrophy in the Russian Federation

International Journal of Neonatal Screening
2023-05-16 | Journal article
Contributors: Kristina Mikhalchuk; Olga Shchagina; Alena Chukhrova; Viktoria Zabnenkova; Polina Chausova; Nina Ryadninskaya; Dmitry Vlodavets; Sergei I. Kutsev; Alexander Polyakov
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Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia

Genes
2022-11-23 | Journal article
Contributors: Valeriia A. Kovalskaia; Victoriia V. Zabnenkova; Marina S. Petukhova; Zhanna G. Markova; Vyacheslav Yu. Tabakov; Oxana P. Ryzhkova
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Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome

The Application of Clinical Genetics
2022-01 | Journal article
Contributors: Viktoriia Zabnenkova; Olga Shchagina; Olga Makienko; Galina Matyushchenko; Oxana Ryzhkova
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Plasma FGF-21 and GDF-15 are elevated in different inherited metabolic diseases and are not diagnostic for mitochondrial disorders

Journal of Inherited Metabolic Disease
2019 | Journal article
EID:

2-s2.0-85069667473

Contributors: Tsygankova, P.G.; Itkis, Y.S.; Krylova, T.D.; Kurkina, M.V.; Bychkov, I.O.; Ilyushkina, A.A.; Zabnenkova, V.V.; Mikhaylova, S.V.; Pechatnikova, N.L.; Sheremet, N.L. et al.
Source: Self-asserted source
Viktoriia Zabnenkova via Scopus - Elsevier

Infantile and early childhood onset of mitochondrial myopathy due to mutations in the TK2 gene with a phenotype of spinal muscular atrophy 5q: the first cases in Russia

Neuromuscular Diseases
2019-11-20 | Journal article
Contributors: S. A. Kurbatov; P. G. Tsygankova; K. Yu. Mollaeva; I. O. Bychkov; Yu. S. Itkis; V. V. Zabnenkova; Z. R. Umakhanova; L. G. Geybatova; E. Yu. Zakharova
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Crossref

HTT Gene Premutation Allele Frequencies in the Russian Federation

Russian Journal of Genetics
2018 | Journal article
EID:

2-s2.0-85049346324

Contributors: Zabnenkova, V.; Schagina, O.A.; Galeeva, N.M.; Kopishinskaya, S.V.; Polyakov, A.V.
Source: Self-asserted source
Viktoriia Zabnenkova via Scopus - Elsevier

SMN1 gene point mutations in type I–IV proximal spinal muscular atrophy patients with a single copy of SMN1

Russian Journal of Genetics
2015 | Journal article
EID:

2-s2.0-84941964781

Contributors: Zabnenkova, V.V.; Dadali, E.L.; Artemieva, S.B.; Sharkova, I.V.; Rudenskaya, G.E.; Polyakov, A.V.
Source: Self-asserted source
Viktoriia Zabnenkova via Scopus - Elsevier

[Genetic and clinical characteristics of 22q11.2 deletion syndrome]

Genetika
2014 | Journal article
EID:

2-s2.0-84925348628

Contributors: Kozlova, Iu.O.; Zabnenkova, V.V.; Shilova, N.V.; Min'zhenkova, M.E.; Antonenko, V.G.; Kotlukova, N.P.; Simonova, L.V.; Kazanceva, I.A.; Levchenko, E.G.; Bombardirova, T.D. et al.
Source: Self-asserted source
Viktoriia Zabnenkova via Scopus - Elsevier

Geneticl and clinical characteristics of 22q11.2 deletion syndrome

Russian Journal of Genetics
2014 | Journal article
EID:

2-s2.0-84901657438

Contributors: Kozlova, Y.O.; Zabnenkova, V.V.; Shilova, N.V.; Min'zhenkova, M.E.; Antonenko, V.G.; Kotlukova, N.P.; Simonova, L.V.; Kazantseva, I.A.; Levchenko, E.G.; Bombardirova, T.D. et al.
Source: Self-asserted source
Viktoriia Zabnenkova via Scopus - Elsevier

[Heterozygous carrier rate for type I-IV proximal spinal muscular atrophy in Chuvashes, Udmurts, and residents of the Moscow region].

Genetika
2012 | Journal article
EID:

2-s2.0-84871885107

Contributors: Zabnenkova, V.V.; Dadali, E.L.; Spiridonova, M.G.; Zinchenko, R.A.; Poliakov, A.V.
Source: Self-asserted source
Viktoriia Zabnenkova via Scopus - Elsevier

Heterozygous carrier rate for type I-IV proximal spinal muscular atrophy in Chuvashes, Udmurts, and residents of the Moscow region

Russian Journal of Genetics
2012 | Journal article
EID:

2-s2.0-84865441823

Contributors: Zabnenkova, V.V.; Dadali, E.L.; Spiridonova, M.G.; Zinchenko, R.A.; Polyakov, A.V.
Source: Self-asserted source
Viktoriia Zabnenkova via Scopus - Elsevier

Peer review (2 reviews for 1 publication/grant)

Review activity for The Egyptian Journal of Medical Human Genetics. (2)