Ekaterina N. Tolmacheva

Tomsk, TOM, Russian Federation

Last Updated: 09/26/2026

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Found 27 publications

A family case of a rare Xq28 duplication.

A family case of a rare Xq28 duplication.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: March 05, 2025

Transposable elements as key regulators of placental development.

Transposable elements as key regulators of placental development.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: February 18, 2025

Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy X.

Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy X.

Journal: Journal of assisted reproduction and genetics

Published: October 25, 2024

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

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss.

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss.

Journal: Nature medicine

Published: May 26, 2023

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

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

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: January 18, 2023

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

Comparative cytogenetics of anembryonic pregnancies and missed abortions in human.

Comparative cytogenetics of anembryonic pregnancies and missed abortions in human.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: September 30, 2022

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

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

Journal: Cytogenetic and genome research

Published: November 09, 2021

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

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

Journal: MethodsX

Published: May 07, 2021

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

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

Journal: Scientific reports

Published: April 30, 2021

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

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

Journal: Journal of assisted reproduction and genetics

Published: April 19, 2021

Showing 1-12 of 27

Last Updated: 09/26/2026