Lyudmila P. Nazarenko

Ushaika Street 10
Tomsk, TOM 634050, Russian Federation

Last Updated: 09/26/2026

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Found 20 publications

Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders.

Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders.

Journal: Molecular cytogenetics

Published: September 02, 2024

Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants.

Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants.

Journal: Genome medicine

Published: May 04, 2024

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

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

Journal: Frontiers in genetics

Published: October 31, 2023

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

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

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: November 08, 2022

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.

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.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: October 13, 2022

Comparision of fluorimetric and mass spectrometric methods for Fabry disease newborn screening.

Comparision of fluorimetric and mass spectrometric methods for Fabry disease newborn screening.

Journal: Klinicheskaia laboratornaia diagnostika

Published: May 16, 2022

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

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

Journal: Genes

Published: November 19, 2020

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

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

Journal: Cytogenetic and genome research

Published: October 12, 2020

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

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

Journal: Stem cell research

Published: September 25, 2020

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

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

Journal: Stem cell research

Published: August 01, 2020

Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy Loss.

Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy Loss.

Journal: Cytogenetic and genome research

Published: January 05, 2020

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

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

Journal: Stem cell research

Published: August 12, 2019

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Last Updated: 09/26/2026