Author

V. V. Petrova

Observed names: Valeria V. Petrova, Valeria Viktorovna Petrova

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: 0000-0003-4400-994X

Observed ORCID: 0000-0003-4400-994X

OpenAlex ID: A5061682813

Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders

2025 · Ekaterina N. Tolmacheva, Anna A. Kashevarova, et al. · Molecular Cytogenetics · 4

Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI

2023 · Irina Zh. Zhalsanova, Anna Evgenievna Postrigan, et al. · International Journal of Molecular Sciences · 3

Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1 Duplications

2024 · A. A. Kashevarova, M. E. Lopatkina, et al. · Molecular Genetics & Genomic Medicine · 2

Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing

2022 · A. A. Sivtsev, I. Zh. Zhalsanova, et al. · Russian Clinical Laboratory Diagnostics · 1

A novel variant of NF1 gene in a patient with neurofibromatosis type 1: a case report

2026 · I. Zh. Zhalsanova, E. A. Fonova, et al. · Siberian Journal of Oncology

A novel homozygous variant in the ATP7B gene in a patient with Wilson’s disease: a case report

2026 · Valentina E. Shavrak, Irina Z. Zhalsanova, et al. · Frontiers in Medicine

Works count: 6

Citation count: 10

H-index: 2

I10-index: