| The ctenophore genome and the evolutionary origins of neural systems LL Moroz, KM Kocot, MR Citarella, S Dosung, TP Norekian, ... Nature 510 (7503), 109-114, 2014 | 761 | 2014 |
| Human-specific histone methylation signatures at transcription start sites in prefrontal neurons HP Shulha, JL Crisci, D Reshetov, JS Tushir, I Cheung, R Bharadwaj, ... PLoS biology 10 (11), e1001427, 2012 | 135 | 2012 |
| Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer’s disease patients and in normal cohorts from Russian populations SA Golenkina, AY Goltsov, IL Kuznetsova, AP Grigorenko, TV Andreeva, ... Molecular biology 44, 546-551, 2010 | 43 | 2010 |
| CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene TV Egorova, ED Zotova, DA Reshetov, AV Polikarpova, SG Vassilieva, ... Disease Models & Mechanisms 12 (4), dmm037655, 2019 | 42 | 2019 |
| Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry MS Protasova, AP Grigorenko, TV Tyazhelova, TV Andreeva, ... European Journal of Human Genetics 24 (4), 550-555, 2016 | 37 | 2016 |
| Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies TV Andreeva, TV Tyazhelova, VN Rykalina, FE Gusev, AY Goltsov, ... Scientific reports 6 (1), 26440, 2016 | 34 | 2016 |
| Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia FE Gusev, DA Reshetov, AC Mitchell, TV Andreeva, A Dincer, ... Translational Psychiatry 9 (1), 256, 2019 | 21 | 2019 |
| Base-calling algorithm with vocabulary (BCV) method for analyzing population sequencing chromatograms YS Fantin, AD Neverov, AV Favorov, MV Alvarez-Figueroa, ... PLoS One 8 (1), e54835, 2013 | 17 | 2013 |
| Therapeutic potential of highly functional codon-optimized microutrophin for muscle-specific expression AV Starikova, VV Skopenkova, AV Polikarpova, DA Reshetov, ... Scientific Reports 12 (1), 848, 2022 | 15 | 2022 |
| Epigenetic-genetic chromatin footprinting identifies novel and subject-specific genes active in prefrontal cortex neurons FE Gusev, DA Reshetov, AC Mitchell, TV Andreeva, A Dincer, ... The FASEB Journal 33 (7), 8161, 2019 | 14 | 2019 |
| SNAD: sequence name annotation-based designer IA Sidorov, DA Reshetov, AE Gorbalenya Bmc Bioinformatics 10, 1-7, 2009 | 9 | 2009 |
| Neurodevelopmental syndrome with intellectual disability, speech impairment, and quadrupedia is associated with glutamate receptor delta 2 gene defect AP Grigorenko, MS Protasova, AA Lisenkova, DA Reshetov, TV Andreeva, ... Cells 11 (3), 400, 2022 | 6 | 2022 |
| Modification of the method for analysis of genome editing results using CRISPR/Cas9 system on preimplantation mouse embryos TV Dimitrieva, DA Reshetov, VE Zhernovkov, DV Vlodavets, ED Zotova, ... Bulletin of Russian State Medical University, 15-20, 2016 | 4 | 2016 |
| DMD TREATMENT: ANIMAL MODELS: P. 203Exons 6 and 7 skipping test on new murine model of Duchenne muscular dystrophy T Egorova, D Reshetov, A Polikarpova, S Vassilieva, D Vlodavets, ... Neuromuscular Disorders 28, S94, 2018 | 3 | 2018 |
| P. 393New advances in the neuromuscular diseases registry in Russia D Vlodavets, A Monakhova, O Shidlovskaya, I Shulyakova, S Artemieva, ... Neuromuscular Disorders 29, S196, 2019 | 2 | 2019 |
| DMD Genetic registry in Russia. D Vlodavets, D Reshetov, S Artemieva, I Shulyakova, O Shidlovskaya, ... Neuromuscular Disorders 27, S128-S129, 2017 | 2 | 2017 |
| Analysis of phenotype expressions of deletions in the dystrophin gene in terms of efficiency of exon skipping as a method for treatment of hereditary dystrophinopathies ED Zotova, DA Reshetov, VE Zhernovkov, DV Vlodovets, TV Dimitrieva, ... Bulletin of Russian State Medical University, 21-26, 2016 | 2 | 2016 |
| P7-2. The evolution of alpha satellite Suprachromosomal Family 5 from orangutan to man: A story of invasion, death and rebirth VA Shepelev, FE Gusev, DA Reshetov, AA Alexandrov, YB Yurov, ... Molecular Phylogenetics, 136-137, 2012 | 2 | 2012 |
| RNA Interference Effectors Selectively Silence the Pathogenic Variant GNAO1 c.607 G > A In Vitro NV Klementieva, EA Lunev, AA Shmidt, EM Loseva, IM Savchenko, ... nucleic acid therapeutics, 2024 | | 2024 |
| Exons 6 and 7 skipping test on new murine model of Duchenne muscular dystrophy T Egorova, D Reshetov, A Polikarpova, S Vassilieva, D Vlodavets, ... NEUROMUSCULAR DISORDERS 28, S94-S94, 2018 | | 2018 |
Evgeny RogaevИнститут общей генетики им. Н.И.Вавилова РАН, the University of Massachusetts Medical SchooПодтвержден адрес электронной почты в домене vigg.ru
