| Anhedonia but not passive floating is an indicator of depressive-like behavior in two chronic stress paradigms M Stepanichev, A Tishkina, M Novikova, I Levshina, S Freiman, ... Acta Neurobiologiae Experimentalis 76 (4), 324-333, 2016 | 35 | 2016 |
| Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy N Voisin, RE Schnur, S Douzgou, SM Hiatt, CF Rustad, NJ Brown, DL Earl, ... The American Journal of Human Genetics 108 (5), 857-873, 2021 | 22 | 2021 |
| Data set on G4 DNA interactions with human proteins M Vlasenok, O Levchenko, D Basmanov, D Klinov, A Varizhuk, ... Data in brief 18, 348-359, 2018 | 16 | 2018 |
| Surface modification with polyallylamines for adhesion of biopolymers and cells OV Morozova, OA Levchenko, ZA Cherpakova, VV Prokhorov, NA Barinov, ... International Journal of Adhesion and Adhesives 92, 125-132, 2019 | 10 | 2019 |
| Protein corona on gold and silver nanoparticles OV Morozova, ON Volosneva, OA Levchenko, NA Barinov, DV Klinov Materials Science Forum 936, 42-46, 2018 | 7 | 2018 |
| Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder DL Polla, MA Farazi Fard, Z Tabatabaei, P Habibzadeh, OA Levchenko, ... Genetics in Medicine 23 (7), 1246-1254, 2021 | 6 | 2021 |
| Complex diagnostics of non-specific intellectual developmental disorder O Levchenko, E Dadali, L Bessonova, N Demina, G Rudenskaya, ... International Journal of Molecular Sciences 23 (14), 7764, 2022 | 4 | 2022 |
| Exome sequencing of 100 patients with intellectual disability O Levchenko, EL Dadali, L Bessonova, N Demina, GE Rudenskaya, ... European Journal of Human Genetics 27 (S2), 1390-1391, 2019 | 3 | 2019 |
| Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report O Levchenko, A Filatova, I Mishina, A Antonenko, M Skoblov Frontiers in Genetics 14, 1197681, 2023 | 1 | 2023 |
| Clinical and genetic characteristics of X-linked mental retardation 102 type caused by novel mutations in the DDX3X gene (OMIM: 300958) EL Dadali, TV Markova, OA Levchenko, AL Chukhrova, OA Shchagina Neuromuscular Diseases 10 (1), 75-80, 2020 | 1 | 2020 |
| Massive parallel sequencing for molecular-genetic diagnosis of mental retardation OA Levchenko, AV Lavrov Zhurnal Nevrologii i Psikhiatrii Imeni SS Korsakova 118 (12), 65-71, 2018 | 1 | 2018 |
| The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study A Borovikov, N Galeeva, A Marakhonov, A Murtazina, V Kadnikova, ... Human Mutation 2024, 2024 | | 2024 |
| Noonan-like phenotype with pathogenic variant in FBXW11 O Levchenko, S Nagieva, A Lavrov EUROPEAN JOURNAL OF HUMAN GENETICS 32, 182-182, 2024 | | 2024 |
| Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9 O Levchenko, I Panchuk, K Kochergin-Nikitsky, I Petrova, S Nagieva, ... Biosystems 235, 105072, 2024 | | 2024 |
| THE IMPORTANCE OF REANALYSIS OF NGS DATA AND FURTHER FUNCTIONAL ANALYSIS ON THE EXAMPLE OF 5 PATIENTS WITH A CLINICALLY DIAGNOSED HYPOPHOSPHATEMIC RICKET. M Sharova, S Papizh, O Levchenko, A Filatova, A Marakhonov, ... PEDIATRIC NEPHROLOGY 37 (11), 2863-2863, 2022 | | 2022 |
| The importance of NGS data reanalysis and further functional analysis: an example of impaired phosphate metabolism M Sharova, S Papizh, O Levchenko, A Filatova, A Marakhonov, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 151-152, 2022 | | 2022 |
| Spectrum of detected genetic variants in NSD1 gene in Patients with Sotos syndrome IV Volodin, FA Ageeva, AI Kalinkin, KO Karandasheva, AS Tanas, ... Medical Genetics 20 (11), 3-11, 2021 | | 2021 |
| TMEM222 is a new cause of autosomal recessive intellectual developmental disorder O Levchenko, N Demina, A Lavrov EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 869-869, 2020 | | 2020 |
| Variants in the degron of AFF3 cause a multi-system disorder with mesomelic dysplasia, horseshoe kidney and developmental and epileptic encephalopathy N Voisin, RE Schnur, S Douzgou, SM Hiatt, CF Rustad, NJ Brown, DL Earl, ... bioRxiv, 693937, 2019 | | 2019 |
| A clinical case of autosomal dominant mental retardation type 49 O Levchenko, E Dadali, A Lavrov EUROPEAN JOURNAL OF HUMAN GENETICS 27, 953-953, 2019 | | 2019 |
