I. Lebedev

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Evolutionary Aspects of Genomic Imprinting

E. Sazhenova, I. Lebedev, 2021 .

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

M. Nazarenko, O. Barbarash, V. Puzyrev, 2011, Molecular Biology.

Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss

V. Stepanov, E. A. Fonova, E. Sazhenova, 2022, Cytogenetic and Genome Research.

Relationship between morphological and cytogenetic heterogeneity in invasive micropapillary carcinoma of the breast: a report of one case

I. Lebedev, N. Cherdyntseva, E. Denisov, 2015, Journal of Clinical Pathology.

Stem Cell-Based Trophoblast Models to Unravel the Genetic Causes of Human Miscarriages

I. Lebedev, T. Nikitina, 2022, Cells.

DNA methylation profiling of the vascular tissues in the setting of atherosclerosis

M. Nazarenko, O. Barbarash, V. Puzyrev, 2013, Molecular Biology.

Epigenetic status of imprinted genes in placenta during recurrent pregnancy loss

E. Sazhenova, I. Lebedev, L. Minaycheva, 2017, Russian Journal of Genetics.

Estimation of the Prevalence and Parental Origin of Chromosomal Microdeletions and Microduplications Affecting the CNTN6 Gene in Patients with Neurodevelopmental Disorders and Healthy Individuals

I. Lebedev, S. Ivanova, M. Lopatkina, 2021 .

Preimplantation genetic diagnosis by blastocentesis: Problems and perspectives

I. Lebedev, N. Skryabin, A. Svetlakov, 2016, Russian Journal of Genetics.

Array CGH analysis of a cohort of Russian patients with intellectual disability.

V. Kučinskas, G. Romeo, E. Sazhenova, 2014, Gene.

Epigenetic status of cell cycle regulation genes in the placenta of human embryos with chromosomal mosaicism

E. Sazhenova, I. Lebedev, E. Tolmacheva, 2011, Molecular Biology.

Evolutionary Aspects of Genomic Imprinting

E. Sazhenova, I. Lebedev, 2021, Molecular Biology.

Pleiotropy of Copy Number Variation in Human Genome

I. Lebedev, A. Kashevarova, G. Drozdov, 2022, Russian Journal of Genetics.

Interloci CNV Interactions in Variability of the Phenotypes of Neurodevelopmental Disorders

I. Lebedev, E. Belyaeva, 2022, Russian Journal of Genetics.

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

I. Lebedev, N. Babushkina, A. Kashevarova, 2016, American journal of medical genetics. Part A.

Effect of the THBS1 Gene Knockout on the Radiation-Induced Cellular Response in a Model System In Vitro

V. Fishman, L. Sukhikh, I. Lebedev, 2020, Russian Journal of Genetics.

X-Linked CNV in Pathogenetics of Intellectual Disability

I. Lebedev, E. Tolmacheva, E. Fonova, 2022, Russian Journal of Genetics.

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

N. Matveeva, V. Fishman, M. Filipenko, 2018, Molecular Neurobiology.

The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes

Yiping Shen, T. Liehr, M. Crimi, 2022, HGG advances.

ADAMTS1 Is Differentially Expressed in Human Lymphocytes with Various Frequencies of Endogenous γH2AX Foci and Radiation-Induced Micronuclei

N. Skryabin, L. Sukhikh, I. Lebedev, 2022, Russian Journal of Genetics.

FISH Diagnostics of Chromosomal Translocation with the Technology of Synthesis of Locus-Specific DNA Probes Based on Long-Range PCR

I. Lebedev, E. Belyaeva, M. Lopatkina, 2020, Russian Journal of Genetics.

Genomic architecture of human chromosomal diseases

I. Lebedev, A. Kashevarova, 2016, Russian Journal of Genetics.

FISH Diagnostics of Chromosomal Translocation with the Technology of Synthesis of Locus-Specific DNA Probes Based on Long-Range PCR

I. Lebedev, E. Belyaeva, M. Lopatkina, 2020, Russian Journal of Genetics.

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

N. Matveeva, V. Fishman, M. Filipenko, 2018, Molecular Neurobiology.

Aneuploidy and DNA Methylation as Mirrored Features of Early Human Embryo Development

I. Lebedev, S. Vasilyev, E. Tolmacheva, 2020, Genes.

Ontogenetic Pleiotropy of Genes Involved in CNVs in Human Spontaneous Abortions

E. Sazhenova, I. Lebedev, A. Kashevarova, 2019, Russian Journal of Genetics.

Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay

V. Fishman, I. Lebedev, E. Belyaeva, 2021, Cytogenetic and Genome Research.

Epigenetic silencing of genomic structural variations

N. Skryabin, I. Lebedev, S. Vasilyev, 2017, Russian Journal of Genetics.

Cytogenetic effects of neutron therapy in patients with parotid gland tumors and relapse of breast cancer.

I. Lebedev, L. Urazova, S. Vasilyev, 2012, Experimental oncology.

Detection of Aneuploidy in Spontaneous Abortions Using Comparative Genomic Hybridization

I. Lebedev, T. V. Nikitina, S. Nazarenko, 2002, Russian Journal of Genetics.

Epigenetic Mosaicism in Genomic Imprinting Disorders

E. Sazhenova, I. Lebedev, 2019, Russian Journal of Genetics.

Variation of DNA copies number in etiology of congenital heart defects

A. A. Slepukhina, I. Lebedev, G. Lifshitz, 2018, Russian Journal of Cardiology.

Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium

T. Schulze, R. Gainetdinov, E. Khusnutdinova, 2019, Molecular Psychiatry.

Clinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal transition and CD44+CD24- stemness

I. Lebedev, J. Wilhelm, N. Cherdyntseva, 2017, Oncotarget.

Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter

I. Lebedev, A. Markov, S. Vasilyev, 2021, MethodsX.

LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidy

E. Sazhenova, I. Lebedev, A. Markov, 2020, Journal of Assisted Reproduction and Genetics.

Mosaic Aneuploidy in Early Fetal Losses

I. Lebedev, Igor N. Lebedev, 2011, Cytogenetic and Genome Research.

Tissue-Specific Placental Mosaicism for Autosomal Trisomies in Human Spontaneous Abortuses: Mechanisms of Formation and Phenotypical Effects

I. Lebedev, S. Nazarenko, 2001, Russian Journal of Genetics.

Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells

E. D. Sorokoumov, S. Zakian, I. Lebedev, 2020, Cytotechnology.

NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss

V. Stepanov, E. Sazhenova, I. Lebedev, 2021, Journal of Assisted Reproduction and Genetics.

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

E. Sazhenova, I. Lebedev, E. Tolmacheva, 2020, Journal of Assisted Reproduction and Genetics.

Multilocus epimutations of imprintome in the pathology of human embryo development

E. Sazhenova, I. Lebedev, N. Skryabin, 2012, Molecular Biology.

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

E. Sazhenova, I. Lebedev, I. N. Lebedev, 2008, Russian Journal of Genetics.

Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis

I. Lebedev, T. V. Nikitina, S. Nazarenko, 2004, European Journal of Human Genetics.

Evaluation of the Role of Uniparental Disomy in Early Embryolethality of Man

E. Sazhenova, I. Lebedev, T. V. Nikitina, 2004, Russian Journal of Developmental Biology.

[Detection of aneuploidy in spontaneous abortions using the comparative hybridization method].

I. Lebedev, T. V. Nikitina, S. Nazarenko, 2002, Genetika.

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

E. Sazhenova, I. Lebedev, M. V. Lepshin, 2014, Russian Journal of Genetics.

Epigenetic status of imprinted genes in placenta during recurrent pregnancy loss

E. Sazhenova, I. Lebedev, L. Minaycheva, 2017, Russian Journal of Genetics.

Chapter 5 Genomic Imprinting and Human Reproduction

I. Lebedev, 2017 .

Genomic Imprinting and Human Reproduction

I. Lebedev, 2014 .

A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss

T. Liehr, J. Pavelić, I. Lebedev, 2018, Cytogenetic and Genome Research.

Multilocus epimutations of imprintome in the pathology of human embryo development

E. Sazhenova, I. Lebedev, N. Skryabin, 2012, Molecular Biology.

[Sex ratio in early embryonal mortality in man].

I. Lebedev, V. Evdokimova, T. V. Nikitina, 2000, Ontogenez.

Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses

E. Sazhenova, I. Lebedev, S. Vasilyev, 2016, Biomedicine Hub.

A mathematical model for evaluation of maternal cell contamination in cultured cells from spontaneous abortions: significance for cytogenetic analysis of prenatal selection factors.

E. Sazhenova, I. Lebedev, T. V. Nikitina, 2005, Fertility and sterility.

About the sex ratio in connection with early embryonic mortality in man

I. Lebedev, V. Evdokimova, T. V. Nikitina, 2000, Russian Journal of Developmental Biology.

Cytogenetics of recurrent pregnancy loss

I. Lebedev, T. Nikitina, 2014, Russian Journal of Genetics.

Epimutations of imprinted genes in the human genome: Classification, causes, association with hereditary pathology

E. Sazhenova, I. Lebedev, 2008, Russian Journal of Genetics.

Epigenetic perspectives of safety in assisted reproductive technologies

I. Lebedev, V. P. Puzyrev, 2007, Russian Journal of Genetics.

Specific Features of Phenotypic Expression of Autosomal Monosomies during Pathological Postimplantation Development of Man

I. Lebedev, S. Nazarenko, 2004, Russian Journal of Developmental Biology.

Maternal Cell Contamination of Cultures of Spontaneous Abortion Fibroblasts: Importance for Cytogenetic Analysis of Embryonic Lethality

E. Sazhenova, I. Lebedev, T. V. Nikitina, 2004, Russian Journal of Genetics.

Molecular Cytogenetic Characteristics of Chromosome Imbalance in Spontaneous Human Abortion Cells with Low Proliferative Activity in Vitro

I. Lebedev, T. V. Nikitina, S. Nazarenko, 2003, Russian Journal of Genetics.

Estimation of the mehylation status of the promoter region of the cell cycle control gene P14ARF in placental tissues of spontaneous abortions with chromosomal mosaicism

E. Sazhenova, I. Lebedev, E. Tolmacheva, 2009, Russian Journal of Genetics.

Chromosomal Instability and Karyotype Correction in Human Induced Pluripotent Stem Cells

I. Lebedev, A. Kashevarova, T. Nikitina, 2019, Russian Journal of Genetics.

Transcriptome Analysis as a Tool for Investigation of Pathogenesis of Chromosomal Diseases

I. Lebedev, M. Lopatkina, 2020, Russian Journal of Genetics.

Aneugenic effect of ionizing radiation in mammalian and human somatic cells

I. Lebedev, S. Vasilyev, V. A. Timoshevsky, 2009, Russian Journal of Genetics.

Estimation of the Prevalence and Parental Origin of Chromosomal Microdeletions and Microduplications Affecting the CNTN6 Gene in Patients with Neurodevelopmental Disorders and Healthy Individuals

I. Lebedev, S. Ivanova, M. Lopatkina, 2021, Russian Journal of Genetics.

Epigenetic regulation and role of LINE-1 retrotransposon in embryogenesis

I. Lebedev, S. Vasilyev, E. Tolmacheva, 2016, Russian Journal of Genetics.

The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing

V. Trifonov, K. Orishchenko, I. Lebedev, 2022, Biomedicines.

BiasCorrector: Fast and accurate correction of all types of experimental biases in quantitative DNA methylation data derived by different technologies

J. Hoheisel, S. Mate, Andrea S Bauer, 2021, International journal of cancer.

Identification of differentially methylated genes in first-trimester placentas with trisomy 16

E. Sazhenova, I. Lebedev, A. Markov, 2022, Scientific reports.

Skewed X-chromosome inactivation in human miscarriages

E. Sazhenova, I. Lebedev, E. Tolmacheva, 2016, Cell and Tissue Biology.

From contemplation to classification of chromosomal mosaicism in human preimplantation embryos

I. Lebedev, D. Zhigalina, 2021, Journal of Assisted Reproduction and Genetics.

A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disability

V. Fishman, G. Romeo, I. Lebedev, 2018, American journal of medical genetics. Part A.

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

I. Lebedev, O. Serov, M. Gridina, 2021, Scientific Reports.

A Comparison of Genome-Wide DNA Methylation Patterns between Different Vascular Tissues from Patients with Coronary Heart Disease

M. Nazarenko, M. Freidin, O. Barbarash, 2015, PloS one.

Dynamics of aberrant methylation of functional groups of genes in progression of breast cancer

I. Lebedev, N. Cherdyntseva, E. Slonimskaya, 2013, Molecular Biology.

Runs of homozygosity in spontaneous abortions from families with recurrent pregnancy loss

I. Lebedev, N. Babushkina, S. Vasilyev, 2019, Vavilov Journal of Genetics and Breeding.

Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22

I. Lebedev, E. Belyaeva, S. Vasilyev, 2018, Molecular Cytogenetics.

46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study

I. Lebedev, E. Belyaeva, A. Zarubin, 2020, Genes.

Effect of ADAMTS1 Differential Expression on the Radiation-Induced Response of HеLа Cell Line

L. Sukhikh, I. Lebedev, A. A. Murashkina, 2021, Russian Journal of Genetics.

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

E. Sazhenova, I. Lebedev, S. Vasilyev, 2015, Molecular Biology.

Derivation of Induced Pluripotent Stem Cells from Fetal Human Skin Fibroblasts

A. G. Shilov, I. Zhimulev, A. Shevchenko, 2010, Acta naturae.

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing

I. Lebedev, A. Makunin, N. Rubtsov, 2021, Biomedicines.

Generation and characterization of iPSCs from human embryonic dermal fibroblasts of a healthy donor from Siberian population

S. Zakian, I. Lebedev, A. Malakhova, 2018, bioRxiv.

Epigenetic effects of trisomy 16 in human placenta

I. Lebedev, E. Tolmacheva, A. Kashevarova, 2013, Molecular Biology.

Epigenetic regulation and role of LINE-1 retrotransposon in embryogenesis

I. Lebedev, S. Vasilyev, E. Tolmacheva, 2016, Russian Journal of Genetics.

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

M. Nazarenko, O. Barbarash, O. Barbarash, 2014, Russian Journal of Genetics.

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

E. Sazhenova, I. Lebedev, S. Vasilyev, 2023, Vavilovskii zhurnal genetiki i selektsii.

Cytogenetics of recurrent pregnancy loss

I. Lebedev, T. V. Nikitina, 2014, Russian Journal of Genetics.

Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene.

I. Lebedev, O. Serov, M. Gridina, 2019, Stem cell research.

Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13.

I. Lebedev, O. Serov, M. Gridina, 2018, Stem cell research.

Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22.

I. Lebedev, O. Serov, M. Gridina, 2018, Stem cell research.

Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication.

I. Lebedev, O. Serov, N. V. Shilova, 2019, Stem cell research.

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability

Z. Tümer, G. Romeo, I. Lebedev, 2014, Molecular Cytogenetics.

Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass.

A. Salumets, A. Kurg, I. Lebedev, 2018, Fertility and Sterility.

The karyotype of the blastocoel fluid demonstrates low concordance with both 1 trophectoderm and inner cell mass 2 Running title : Genomic profiling of BF , TE and ICM 3

A. Salumets, A. Kurg, I. Lebedev, 2019 .

Molecular karyotyping of cell-free DNA from blastocoele fluid as a basis for noninvasive preimplantation genetic screening of aneuploidy

I. A. Stepanov, I. Lebedev, N. Skryabin, 2015, Russian Journal of Genetics.

Epigenetic silencing of genomic structural variations

I. Lebedev, S. Vasilyev, N. Skryabin, 2017, Russian Journal of Genetics.

A cookbook for DNase Hi-C

E. Mozheiko, V. Fishman, I. Lebedev, 2021, Epigenetics & chromatin.

Frequencies of C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene at the early stage of human development

M. Nazarenko, I. Lebedev, V. P. Puzyrev, 2006, Russian Journal of Genetics.

Skewed X-chromosome inactivation in human miscarriages

E. Sazhenova, I. Lebedev, S. A. Vasil’ev, 2016, Cell and Tissue Biology.

Skewed X-chromosome inactivation in human embryos with mosaic trisomy 16

V. Kharkov, I. Lebedev, E. Tolmacheva, 2011, Russian Journal of Genetics.

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

I. Lebedev, E. Belyaeva, O. Serov, 2020, Stem cell research.

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

I. Lebedev, O. Serov, M. Gridina, 2020, Stem cell research.

I. Lebedev, J. Wilhelm, N. Cherdyntseva, 2017, Oncotarget.

DNA methylation profile in human placental tissues

I. Lebedev, E. Tolmacheva, A. Kashevarova, 2011, Molecular Biology.

Epigenetic inactivation of the RB1 gene as a factor of genomic instability: A possible contribution to etiology of chromosomal mosaicism during human embryo development

E. Sazhenova, I. Lebedev, E. Tolmacheva, 2008, Russian Journal of Genetics.

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

I. Lebedev, E. Belyaeva, M. Gridina, 2023, Vavilovskii zhurnal genetiki i selektsii.

Generation and application of dynamic standard reference intervals for analyzing results of comparative genomic hybridization

I. Lebedev, V. Zemlyakova, T. V. Zolotukhina, 2013, Russian Journal of Genetics.

Dynamics of aberrant methylation of functional groups of genes in progression of breast cancer

I. Lebedev, N. Cherdyntseva, E. Slonimskaya, 2013, Molecular Biology.

Estimation of association of CNTN6 copy number variation with idiopathic intellectual disability

I. Lebedev, A. Kashevarova, M. Lopatkina, 2016, Russian Journal of Genetics.

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability

Z. Tümer, G. Romeo, I. Lebedev, 2014, Molecular Cytogenetics.

Regulation of karyotype stability in human induced pluripotent stem cells

T. V. Nikitina, I. Lebedev, 2018 .

Germline Mutations of Tetranucleotide DNA Repeats in Families with Normal Children and Reproductive Pathology

I. Lebedev, T. V. Nikitina, S. Nazarenko, 2005, Russian Journal of Genetics.