Author details

Full Name

Oleg V Evgrafov

Affiliation

ORCID

Career Start Year

1978

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37034711	Cultured Mesenchymal Cells from Nasal Turbinate as a Cellular Model of the Neurodevelopmental Component of Schizophrenia Etiology.		2023
38093720	Cell Type Catalog of Middle Turbinate Epithelium ().		2023
37895019	Cultured Mesenchymal Cells from Nasal Turbinate as a Cellular Model of the Neurodevelopmental Component of Schizophrenia Etiology.		2023
34946185	and Negatively Interact during Oxidative Stress.	Microorganisms	2021
32561870	Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain.	Sci Data	2020
32143829	Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia.	Biol Psychiatry	2020
32029778	Robust RNA-Seq of aRNA-amplified single cell material collected by patch clamp.	Scientific Reports	2020
31535015	Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia.	Sci Adv	2019
29961565	Endogenous Cell Type-Specific Disrupted in Schizophrenia 1 Interactomes Reveal Protein Networks Associated With Neurodevelopmental Disorders.	Biol Psychiatry	2019
31440583	Complete Mitochondrial Genome Sequences of Five Rockfishes (Perciformes: ).	Mitochondrial DNA Part B: Resources	2018
30555922	Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation.	Sci Adv	2018
30545854	Integrative functional genomic analysis of human brain development and neuropsychiatric risks.	Science	2018
29942251	Analysis of Gene Expression Variance in Schizophrenia Using Structural Equation Modeling.	Frontiers in Molecular Neuroscience	2018
27965293	Reconstructing genetic history of Siberian and Northeastern European populations.	Genome Res	2017
28671696	Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders.	Nat Neurosci	2017
28030860	Transcriptional Gene Silencing of the Autism-Associated Long Noncoding RNA MSNP1AS in Human Neural Progenitor Cells.	Developmental Neuroscience	2016
27356984	Long-read sequencing and de novo assembly of a Chinese genome.	Nat Commun	2016
26178595	EphA7 regulates spiral ganglion innervation of cochlear hair cells.	Dev Neurobiol	2016
27690106	Impact of the Autism-Associated Long Noncoding RNA MSNP1AS on Neuronal Architecture and Gene Expression in Human Neural Progenitor Cells.	Genes	2016
27881084	Assessing characteristics of RNA amplification methods for single cell RNA sequencing.	BMC Genomics	2016
25989142	The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes.	Transl Psychiatry	2015
26053433	Non-coding RNAs derived from an alternatively spliced REST transcript (REST-003) regulate breast cancer invasiveness.	Sci Rep	2015
24755890	Evidence for linkage and association of GABRB3 and GABRA5 to panic disorder.	Neuropsychopharmacology	2014
25339126	Effect of RNA integrity on uniquely mapped reads in RNA-Seq.	BMC Research Notes	2014
23555279	The conserved SKN-1/Nrf2 stress response pathway regulates synaptic function in Caenorhabditis elegans.	PLoS Genetics	2013
24150225	Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.	Transl Psychiatry	2013
23192985	Assessing the efficacy of endoscopic office olfactory biopsy sites to produce neural progenitor cell cultures for the study of neuropsychiatric disorders.	International Forum of Allergy and Rhinology	2013
22934102	Single-neuron RNA-Seq: technical feasibility and reproducibility.	Front Genet	2012
21795323	RseqFlow: workflows for RNA-Seq data analysis.		2011
21451437	Olfactory neuroepithelium-derived neural progenitor cells as a model system for investigating the molecular mechanisms of neuropsychiatric disorders.	Psychiatric Genetics	2011
20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Mol Psychiatry	2011
19806148	Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.	Mol Psychiatry	2011
18452185	Association and linkage analysis of candidate genes GRP, GRPR, CRHR1, and TACR1 in panic disorder.	Am J Med Genet B Neuropsychiatr Genet	2009
18367154	Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3.	Biol Psychiatry	2008
17267788	Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers.	Am J Psychiatry	2007
17409192	Genomewide suggestive linkage of opioid dependence to chromosome 14q.	Human Molecular Genetics	2007
16919526	A third-pass genome scan in panic disorder: evidence for multiple susceptibility loci.	Biol Psychiatry	2006
17178704	A novel splicing mutation in exon 4 (456G>A) of the GH1 gene in a patient with congenital isolated growth hormone deficiency.	Hormones	2006
17073157	GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children.	Bulletin of Experimental Biology and Medicine	2006
15021985	A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.	Hum Genet	2004
15186961	Population-based study of SR-BI genetic variation and lipid profile.	Atherosclerosis	2004
15122254	Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.	Nature Genetics	2004
14564781	[Proximal autosomal recessive types of spinal muscular atrophy].	Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova	2003
12574219	A novel IVS2 -2A>T splicing mutation in the GH-1 gene in familial isolated growth hormone deficiency type II in the spectrum of other splicing mutations in the Russian population.	Journal of Clinical Endocrinology and Metabolism	2003
12833396	657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls.	American Journal of Medical Genetics, Part A	2003
12830434	BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.	Am J Hum Genet	2003
11810107	Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.	Nature Genetics	2002
11953735	Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families.	J Pediatr	2002
11313751	On the origin and frequency of the 35delG allele in GJB2-linked deafness in Europe.	European Journal of Human Genetics	2001
11528513	A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.	European Journal of Human Genetics	2001