about
The evolutionary origin of man can be traced in the layers of defunct ancestral alpha satellites flanking the active centromeres of human chromosomesAneuploidy and confined chromosomal mosaicism in the developing human brain.Human interphase chromosomes: a review of available molecular cytogenetic technologies.Trisomy 21 mosaicism: we may all have a touch of Down syndrome.In silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for basic and clinical genome research.Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain.Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism.Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy.Single cell genomics of the brain: focus on neuronal diversity and neuropsychiatric diseases.5p13.3p13.2 duplication associated with developmental delay, congenital malformations and chromosome instability manifested as low-level aneuploidy.3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances.GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny.X chromosome aneuploidy in the Alzheimer's disease brain.SINE and LINE within human centromeres.Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB).An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.Annotation of suprachromosomal families reveals uncommon types of alpha satellite organization in pericentromeric regions of hg38 human genome assembly.Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the diseaseMolecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.Unexplained autism is frequently associated with low-level mosaic aneuploidy.Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning.5HTR2A gene polymorphism and personality traits in patients with major psychoses.The units of DNA replication in the mammalian chromosomes: evidence for a large size of replication units.Interspersed repeats are found predominantly in the "old" alpha satellite families.First case of del(1)(p36.2p33) in a fetus delivered stillborn.Genetic and physical analyses of the centromeric and pericentromeric regions of human chromosome 5: recombination across 5cen.Unequal cross-over is involved in human alpha satellite DNA rearrangements on a border of the satellite domain.Genomic organization, sequence and polymorphism of the human chromosome 4-specific alpha-satellite DNA.Somatic cell genomics of brain disorders: a new opportunity to clarify genetic-environmental interactions.DNA replication in human diploid cells of different origin.Ataxia telangiectasia paradox can be explained by chromosome instability at the subtissue level.Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome.Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys).Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases.Mosaic X chromosome aneuploidy can help to explain the male-to-female ratio in autism.Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrity.Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes.The DNA replication stress hypothesis of Alzheimer's disease.Genomic landscape of the Alzheimer's disease brain: chromosome instability--aneuploidy, but not tetraploidy--mediates neurodegeneration.Recent patents on molecular cytogenetics.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
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հետազոտող
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name
Yuri B. Yurov
@ast
Yuri B. Yurov
@en
Yuri B. Yurov
@es
Yuri B. Yurov
@nl
Yuri B. Yurov
@sl
type
label
Yuri B. Yurov
@ast
Yuri B. Yurov
@en
Yuri B. Yurov
@es
Yuri B. Yurov
@nl
Yuri B. Yurov
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prefLabel
Yuri B. Yurov
@ast
Yuri B. Yurov
@en
Yuri B. Yurov
@es
Yuri B. Yurov
@nl
Yuri B. Yurov
@sl
P1053
D-9051-2016
P106
P1153
7006321243
P21
P31
P3829
P496
0000-0002-9251-2286