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Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming

Scientific reports, 2021-02, Vol.11 (1), p.4325-4325, Article 4325

2021

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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability

European psychiatry, 2023-03, Vol.66 (S1), p.S887-S887

2023

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A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication

Frontiers in genetics, 2024, Vol.15, p.1331066-1331066

2024

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Comparative cytogenetics of anembryonic pregnancies and missed abortions in human

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2023-03, Vol.27 (1), p.28-35

2023

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Aberrant methylation of placental development genes in chorionic villi of spontaneous abortions with trisomy 16

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2024-04, Vol.28 (2), p.198-203

2024

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Influence of human peripheral blood samples preprocessing on the quality of Hi-C libraries

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2023-03, Vol.27 (1), p.83-87

2023

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Expression of the NUP153 and YWHAB genes from their canonical promoters and alternative promoters of the LINE-1 retrotransposon in the placenta of the first trimester of pregnancy

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2023-03, Vol.27 (1), p.63-71

2023

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The Use of Thyristor Switches in the Power Supply of Nuclotron Booster Inflector Plates

Physics of particles and nuclei letters, 2023-08, Vol.20 (4), p.763-766

2023

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Evolutionary Aspects of Genomic Imprinting

Molecular biology (New York), 2021, Vol.55 (1), p.1-15

2021

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On the 40th anniversary of the Research Institute of Medical Genetics, Tomsk National Research Medical Center

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2023-03, Vol.27 (1), p.5-6

2023

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Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss

Journal of assisted reproduction and genetics, 2020-03, Vol.37 (3), p.517-525

2020

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Cytogenetics of recurrent pregnancy loss

Russian journal of genetics, 2014-05, Vol.50 (5), p.435-446

2014

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Somatic genome variations in vascular tissues and peripheral blood leukocytes in patients with atherosclerosis

Genetika, 2014-08, Vol.50 (8), p.870-878

2014

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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies

European psychiatry, 2023-03, Vol.66 (S1), p.S887-S887

2023

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Multiple epimutations in imprinted genes in the human genome and congenital disorders

Russian journal of genetics, 2014-03, Vol.50 (3), p.221-236

2014

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Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4

Stem cell research, 2022-05, Vol.61, p.102740-102740, Article 102740

2022

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Methylation status of LINE-1 retrotransposon in chromosomal mosaicism during early stages of human embryonic development

Molecular biology (New York), 2015, Vol.49 (1), p.144-152

2015

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Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18

Stem cell research, 2020-12, Vol.49, p.102076-102076, Article 102076

2020

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Simulation and Equipment for Magnetic Measurements on a Prototype Iron-Free Kicker Magnet with Impacting-Pulse Flat-Top Correction

Physics of particles and nuclei letters, 2018-12, Vol.15 (7), p.860-862

2018

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Methylation profiling of DNA in the area of atherosclerotic plaque in humans

Molecular biology (New York), 2011-08, Vol.45 (4), p.561-566

2011

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Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson’s disease

Stem cell research, 2020-08, Vol.47, p.101922-101922, Article 101922

2020

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Cytogenetic mechanisms of aneuploidy in somatic cells of chemonuclear industry professionals with incorporated plutonium-239

Russian journal of genetics, 2010-11, Vol.46 (11), p.1381-1385

2010

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Generation of Induced Pluripotent Stem Cell Line iTAF15Xsk4 from Fibroblasts of a Patient with Microdeletion at Xq24

Russian journal of developmental biology, 2023, Vol.54 (6), p.358-364

2023

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Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,–8 mosaicism

Stem cell research, 2020-12, Vol.49, p.102024-102024, Article 102024

2020

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Epimutations of the KCNQ1OT1 imprinting center of chromosome 11 in early human embryolethality

Russian journal of genetics, 2008-12, Vol.44 (12), p.1394-1399

2008

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Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming

Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability

A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication

Comparative cytogenetics of anembryonic pregnancies and missed abortions in human

Aberrant methylation of placental development genes in chorionic villi of spontaneous abortions with trisomy 16

Influence of human peripheral blood samples preprocessing on the quality of Hi-C libraries

Expression of the NUP153 and YWHAB genes from their canonical promoters and alternative promoters of the LINE-1 retrotransposon in the placenta of the first trimester of pregnancy

The Use of Thyristor Switches in the Power Supply of Nuclotron Booster Inflector Plates

Evolutionary Aspects of Genomic Imprinting

On the 40th anniversary of the Research Institute of Medical Genetics, Tomsk National Research Medical Center

Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss

Cytogenetics of recurrent pregnancy loss

Somatic genome variations in vascular tissues and peripheral blood leukocytes in patients with atherosclerosis

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies

Multiple epimutations in imprinted genes in the human genome and congenital disorders

Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4

Methylation status of LINE-1 retrotransposon in chromosomal mosaicism during early stages of human embryonic development

Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18

Simulation and Equipment for Magnetic Measurements on a Prototype Iron-Free Kicker Magnet with Impacting-Pulse Flat-Top Correction

Methylation profiling of DNA in the area of atherosclerotic plaque in humans

Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson’s disease

Cytogenetic mechanisms of aneuploidy in somatic cells of chemonuclear industry professionals with incorporated plutonium-239

Generation of Induced Pluripotent Stem Cell Line iTAF15Xsk4 from Fibroblasts of a Patient with Microdeletion at Xq24

Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,–8 mosaicism

Epimutations of the KCNQ1OT1 imprinting center of chromosome 11 in early human embryolethality

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