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Olga A. Levchenko

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy
2021 · Norine Voisin, Rhonda E. Schnur, et al. · The American Journal of Human Genetics · 42
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Anhedonia but not passive floating is an indicator of depressive‑like behavior in two chronic stress paradigms
2016 · Mikhail Yu. Stepanichev, Anna O. Tishkina, et al. · Acta Neurobiologiae Experimentalis · 40
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Data set on G4 DNA interactions with human proteins
2018 · M. Vlasenok, O. Levchenko, et al. · Data in Brief · 14
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Complex Diagnostics of Non-Specific Intellectual Developmental Disorder
2022 · Olga Levchenko, Elena Dadali, et al. · International Journal of Molecular Sciences · 11
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Surface modification with polyallylamines for adhesion of biopolymers and cells
2019 · Olga V. Morozova, Olga A. Levchenko, et al. · International Journal of Adhesion and Adhesives · 10
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
2021 · Daniel L. Polla, Mohammad Ali Farazi Fard, et al. · Genetics in Medicine · 9
The Promise and Pitfalls of AAV-Mediated Gene Therapy for Duchenne Muscular Dystrophy
2025 · Elizaveta V. Kurshakova, Olga A. Levchenko, et al. · Current Issues in Molecular Biology · 6
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Protein Corona on Gold and Silver Nanoparticles
2018 · Olga V. Morozova, Olga N. Volosneva, et al. · Materials science forum · 6
Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders
2024 · Elisa Cali, Tania Quirin, et al. · Genetics in Medicine · 5
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Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report
2023 · Olga Levchenko, Alexandra Filatova, et al. · Frontiers in Genetics · 5
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The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study
2024 · Artem Borovikov, Nailya Galeeva, et al. · Human Mutation · 3
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Autosomal dominant intellectual disability associated with the MED13L gene
2022 · O. A. Levchenko, G. E. Rudenskaya, et al. · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) · 2
Clinical and genetic characteristics of X-linked mental retardation 102 type caused by novel mutations in the DDX3X gene (OMIM:300958)
2020 · E. L. Dadali, T. V. Markova, et al. · Neuromuscular Diseases · 2
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Clinical and molecular genetic features of cases of Floating-Harbor syndrome
2025 · N. A. Makretskaya, O. R. Ismagilova, et al. · Problems of Endocrinology · 1
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Challenges in developing gene therapy against Duchenne muscular dystrophy
2025 · Elizaveta V. Kurshakova, Olga A. Levchenko, et al. · Genes and Cells · 1
Clinical Case of Mild Tatton–Brown–Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene
2024 · Fatima Bostanova, Olga Levchenko, et al. · Clinics and Practice · 1
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Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9
2023 · Olga Levchenko, Irina Panchuk, et al. · Biosystems · 1
Massive parallel sequencing for molecular-genetic diagnosis of mental retardation
2018 · O. A. Levchenko, A. V. Lavrov · S S Korsakov Journal of Neurology and Psychiatry · 1
Surface modification with polyallylamines for immobilization of biopolymers and cells
2018 · Nikolay A. Barinov, Morozova Ov, et al. · FEBS Open Bio
Cohen syndrome in family members: a case report
2017 · O. A. Levchenko, R. A. Zinchenko, et al. · Bulletin of Russian State Medical University
Works count: 20
Citation count: 160
H-index: 6
I10-index: 5
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