Author

Victoria V. Demeneva

Observed names: V. V. Demeneva, V.V. Demeneva, Viktoria V. Demeneva, Деменева В.В., Деменева Виктория Вадимовна

Institutions: Research Institute of Medical Genetics of Russian Academy of Medical Sciences, Tomsk National Research Medical Center

Observed institutions: Russian Academy of Sciences, Research Institute of Medical Genetics of Russian Academy of Medical Sciences, Tomsk National Research Medical Center

ORCID: 0000-0002-5315-4914

Observed ORCID: 0000-0002-5315-4914

OpenAlex ID: A5012329801

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss

2023 · Rick Essers, Igor N. Lebedev, et al. · Nature Medicine · 88

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Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter

2021 · Stanislav A. Vasilyev, Anton V. Markov, et al. · MethodsX · 6

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Identification of differentially methylated genes in first-trimester placentas with trisomy 16

2022 · Ekaterina N. Tolmacheva, Stanislav A. Vasilyev, et al. · Scientific Reports · 5

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Expression of the NUP153 and YWHAB genes from their canonical promoters and alternative promoters of the LINE-1 retrotransposon in the placenta of the first trimester of pregnancy

2023 · V. V. Demeneva, E. N. Tolmacheva, et al. · Vavilov Journal of Genetics and Breeding · 4

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Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy X

2025 · Ekaterina N. Tolmacheva, Daria I. Zhigalina, et al. · Journal of Assisted Reproduction and Genetics

A variant of p.Arg1623Gln of the DYNC1H1 gene in a patient with corpus callosum agenesis, polydactyly, mental development disorder, and neuromuscular system disorders

2025 · A.S. Zuev, E.A. Fonova, et al. · S S Korsakov Journal of Neurology and Psychiatry

Comparative analysis of chorionic methylation abnormalities in various pregnancy pathologies

2025 · Andrew S. Zuev, Daniil G. Shevtsov, et al. · Vestnik Tomskogo gosudarstvennogo universiteta Biologiya

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Молекулярно-цитогенетическая диагностика парацентрической инверсии 8p23.1 в кариотипе матери пациента с invdupdel(8p) на кольцевой хромосоме 8

2024 · Кашеварова А.А., Деменева В.В., et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»

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Abnormal methylation of PRDM16 and PTPRN2 genes in chorionic villi in miscarriage

2023 · Stanislav A. Vasilyev, Oksana Yu. Vasilyeva, et al. · RUDN Journal of Medicine

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Methylation of the Retrotransposon LINE-1 Subfamilies in Chorionic Villi of Miscarriages

2023 · S. A. Vasilyev, V. V. Demeneva, et al. · Russian Journal of Genetics

Methylation of the Retrotransposon LINE-1 Subfamilies in Chorionic Villi of Miscarriages

2023 · S. A. Vasilyev, V. V. Demeneva, et al. · Генетика

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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies

2023 · E. A. Fonova, A. A. Kashevarova, et al. · European Psychiatry

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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability

2023 · A. A. Kashevarova, E. O. Belyaeva, et al. · European Psychiatry

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Сравнительный анализ аномалий метилома хориона при различных патологиях беременности

· Зуев Андрей Сергеевич, Шевцов Даниил Геннадьевич, et al. · CyberLeninK (CyberLeninka)

Works count: 15

Citation count: 103

H-index: 4

I10-index: 1