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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.
Int J Mol Sci. 2024 Nov 13;25(22):12169. doi: 10.3390/ijms252212169.
Int J Mol Sci. 2024.
PMID: 39596236
Free PMC article.
Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas.
Borovikov A, Marakhonov A, Murtazina A, Davydenko K, Filatova A, Galeeva N, Kadnikova V, Ogorodova N, Gorodilova D, Kanivets I, Pyankov D, Zherdev K, Petel'guzov A, Zubkov P, Polyakov A, Shchagina O, Skoblov M.
Borovikov A, et al. Among authors: ogorodova n.
Front Genet. 2024 Aug 13;15:1435493. doi: 10.3389/fgene.2024.1435493. eCollection 2024.
Front Genet. 2024.
PMID: 39192890
Free PMC article.
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A Molecular Genetic Analysis of RPE65-Associated Forms of Inherited Retinal Degenerations in the Russian Federation.
Stepanova A, Ogorodova N, Kadyshev V, Shchagina O, Kutsev S, Polyakov A.
Stepanova A, et al. Among authors: ogorodova n.
Genes (Basel). 2023 Nov 9;14(11):2056. doi: 10.3390/genes14112056.
Genes (Basel). 2023.
PMID: 38002999
Free PMC article.
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Clinical and Genetic Characteristics of Multiple Epiphyseal Dysplasia Type 4.
Markova T, Kenis V, Melchenko E, Alieva A, Nagornova T, Orlova A, Ogorodova N, Shchagina O, Polyakov A, Dadali E, Kutsev S.
Markova T, et al. Among authors: ogorodova n.
Genes (Basel). 2022 Aug 24;13(9):1512. doi: 10.3390/genes13091512.
Genes (Basel). 2022.
PMID: 36140680
Free PMC article.
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