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Natalya Ogorodova

Observed names: N. Yu. Ogorodova, Natalia Ogorodova, Natalya Yu. Ogorodova, Natalya Yu. Ogorodova
ORCID: 0000-0001-6151-5022
Observed ORCID: 0000-0001-6151-5022
OpenAlex ID: A5001851746
Clinical and Genetic Characteristics of Multiple Epiphyseal Dysplasia Type 4
2022 · Tatiana Markova, Vladimir Kenis, et al. · Genes · 22
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A Molecular Genetic Analysis of RPE65-Associated Forms of Inherited Retinal Degenerations in the Russian Federation
2023 · Anna Stepanova, Natalya Ogorodova, et al. · Genes · 7
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Experience in the toothpaste’s hygienic effectiveness assessment by oral fluid biochemical parameters
2022 · S. N. Gromova, A. V. Elikov, et al. · Pediatric dentistry and dental prophylaxis · 7
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Development of Step-by-step Method for Producing Silver Nanoparticles by Citrate Method
2020 · Natalya V. Bogacheva, Ksenia A. Tarbeeva, et al. · IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA · 5
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A Comparative Evaluation of the Genetic Variant Spectrum in the USH2A Gene in Russian Patients with Isolated and Syndromic Forms of Retinitis Pigmentosa
2024 · Natalya Ogorodova, Anna Stepanova, et al. · International Journal of Molecular Sciences · 3
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Clinical, genetic, and orthopedic characteristics of large group of patients with diastrophic dysplasia
2024 · Darya V. Gorodilova, Tatiana V. Markova, et al. · Pediatric Traumatology Orthopaedics and Reconstructive Surgery · 2
Principles of the differential diagnosis of achondroplasia and pseudoachondroplasia
2023 · Tatiana V. Markova, Vladimir M. Kenis, et al. · Pediatric Traumatology Orthopaedics and Reconstructive Surgery · 2
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Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas
2024 · Artem Borovikov, Andrey Marakhonov, et al. · Frontiers in Genetics · 1
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Frequent Genetic Variants of Autosomal Recessive Nonsyndromic Forms of Inherited Retinal Diseases in the Russian Federation
2024 · N. Yu. Ogorodova, A. A. Stepanova, et al. · Russian Journal of Genetics · 1
Whole-Genome Sequencing in Diagnostics of Unsolved Cases of Inherited Retinal Diseases
2026 · Natalya Ogorodova, Anna Stepanova, et al. · International Journal of Molecular Sciences
Delineating the phenotypic spectrum of SLC26A2-related skeletal dysplasias in a cohort of 115 patients: Evidence for a novel complex allele modifying disease severity
2026 · Daria Gorodilova, Tatiana Markova, et al. · Genetics in Medicine
Frequent genetic variants of autosomal recessive non-syndromic forms of inherited retinal diseases in the Russian Federation
2024 · N. Yu. Ogorodova, A. A. Stepanova, et al. · Генетика
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Works count: 12
Citation count: 50
H-index: 4
I10-index: 1
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