about
Genomic structural variations for cardiovascular and metabolic comorbiditySingle gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability.A comparison of genome-wide DNA methylation patterns between different vascular tissues from patients with coronary heart diseaseClinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal transition and CD44+CD24- stemness.Mosaic aneuploidy in early fetal losses.Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis.[Generation and application of dynamic standard reference intervals for analyzing results of comparative genomic hybridization].Array CGH analysis of a cohort of Russian patients with intellectual disability.[Methylation profile of INK4B-ARF-INK4A locus in atherosclerosis].[DNA methylation profiling of the vascular tissues in the setting of atherosclerosis].Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene.Relationship between morphological and cytogenetic heterogeneity in invasive micropapillary carcinoma of the breast: a report of one case.A mathematical model for evaluation of maternal cell contamination in cultured cells from spontaneous abortions: significance for cytogenetic analysis of prenatal selection factors.A de novo microtriplication at 4q21.21-q21.22 in a patient with a vascular malignant hemangioma, elongated sigmoid colon, developmental delay, and absence of speech.Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22.[Epigenetic effects of trisomy 16 in the human placenta]Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell massKaryotype evaluation of repeated abortions in primary and secondary recurrent pregnancy lossGeneration of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disabilityGeneration of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortiumA mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disability
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Igor Lebedev
@en
Igor N Lebedev
@ast
Igor N Lebedev
@es
Igor N Lebedev
@nl
Igor Nikolajewitsch Lebedew
@de
Игорь Николаевич Лебедев
@ru
type
label
Igor Lebedev
@en
Igor N Lebedev
@ast
Igor N Lebedev
@es
Igor N Lebedev
@nl
Igor Nikolajewitsch Lebedew
@de
Игорь Николаевич Лебедев
@ru
altLabel
Igor Lebedew
@de
Igor N Lebedev
@en
Igor Nikolayevich Lebedev
@en
prefLabel
Igor Lebedev
@en
Igor N Lebedev
@ast
Igor N Lebedev
@es
Igor N Lebedev
@nl
Igor Nikolajewitsch Lebedew
@de
Игорь Николаевич Лебедев
@ru
P106
P1153
7103250270
P21
P31
P496
0000-0002-0482-8046