Elena O. Belyaeva

Ushaika Street 10
Tomsk, TOM 634050, Russian Federation

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 10 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

Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single-Gene BDH1 Duplications.

Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single-Gene BDH1 Duplications.

Journal: Molecular genetics & genomic medicine

Published: April 08, 2024

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

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

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

Journal: Stem cell research

Published: February 14, 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

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

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

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

Journal: Molecular cytogenetics

Published: January 08, 2018

Showing 1-10 of 10

Last Updated: 09/26/2026