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Author Details

Denis A Reshetov
2009
12
8
PMIDPaper TitleJournal TitlePublished Year
35159210Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect.Cells2022
35039573Therapeutic potential of highly functional codon-optimized microutrophin for muscle-specific expression.Scientific Reports2022
30970224Epigenetic-genetic chromatin footprinting identifies novel and subject-specific genes active in prefrontal cortex neurons.FASEB J2019
31624234Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia.Transl Psychiatry2019
31028078CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human gene.DMM Disease Models and Mechanisms2019
26242992Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry.European Journal of Human Genetics2016
27216912Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.Scientific Reports2016
24847885The ctenophore genome and the evolutionary origins of neural systems.Nature2014
23382983Base-calling algorithm with vocabulary (BCV) method for analyzing population sequencing chromatograms.PLoS One2013
23185133Human-specific histone methylation signatures at transcription start sites in prefrontal neurons.PLoS Biol2012
20873220[Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer's disease patients and in normal cohorts from Russian populations].Molekulyarnaya Biologiya2010
19682364SNAD: Sequence Name Annotation-based Designer.BMC Bioinformatics2009
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