Valeriia Danilchenko

Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss

O. Posukh, E. A. Maslova, M. V. Zytsar, 2022, International journal of molecular sciences.

Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia)

O. Posukh, E. A. Maslova, N. Barashkov, 2021, Diagnostics.

High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect

O. Posukh, E. A. Maslova, N. Barashkov, 2020, Genes.

Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

O. Posukh, N. Barashkov, A. Bondar, 2018, BMC Medical Genetics.

Gene therapy for Angelman Syndrome: Contemporary approaches and future endeavors.

C. Tsagkaris, L. Matiashova, V. Papakosta, 2020, Current gene therapy.

Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia)

O. Posukh, E. A. Maslova, K. Orishchenko, 2023, Genes.

Children growing up in conflict zones in Ukraine and beyond need urgent mental health support

M. Y. Essar, C. Tsagkaris, L. Matiashova, 2022, The Lancet.