N. Skryabin

发表

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.

Epigenetic status of imprinted genes in placenta during recurrent pregnancy loss

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

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.

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.

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.

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.

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.

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.

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.

Multilocus epimutations of imprintome in the pathology of human embryo development

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

Epigenetic status of imprinted genes in placenta during recurrent pregnancy loss

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

Multilocus epimutations of imprintome in the pathology of human embryo development

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

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

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

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.

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.

Phenotypic Drift as a Cause for Intratumoral Morphological Heterogeneity of Invasive Ductal Breast Carcinoma Not Otherwise Specified

N. Cherdyntseva, E. Denisov, E. Slonimskaya, 2013, BioResearch open access.

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.

Genomic structural variations for cardiovascular and metabolic comorbidity

M. Nazarenko, O. Barbarash, M. Golubenko, 2017, Scientific Reports.

Epigenetic effects of trisomy 16 in human placenta

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

Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI

V. Stepanov, A. E. Postrigan, I. Zhalsanova, 2023, International Journal of Molecular Sciences.

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.

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.

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.

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

DNA methylation profile in human placental tissues

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

Gene Expression Profiling Revealed 2 Types of Bronchial Basal Cell Hyperplasia and Squamous Metaplasia With Different Progression Potentials

E. Denisov, O. Pankova, T. Gerashchenko, 2019, Applied immunohistochemistry & molecular morphology : AIMM.

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

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

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.