Elena A Bliznetz (E A Bliznets, Elena Bliznetz, Elena Bliznets)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Topics

Spectrum Disorder

Top Venues

Journal of personalized medicine

Vestnik otorinolaringologii

This page only lists publications with an associated author ORCID identifier.

Publications

Olga A Shchagina, Elena Gracheva, Alyona Chukhrova, Elena A Bliznetz, Igor O Bychkov, Sergey Kutsev, Aleksander Polyakov
Functional Characterization of Two Novel Intron 4 SERPING1 Gene Splice Site Pathogenic Variants in Families with Hereditary Angioedema. Biomedicines 12 (1) (2023)
Olga A Shchagina, Elena Gracheva, Alyona Chukhrova, Elena A Bliznetz, Igor O Bychkov, Sergey Kutsev, Aleksander Polyakov
Functional Characterization of Two Novel Intron 4 SERPING1 Gene Splice Site Pathogenic Variants in Families with Hereditary Angioedema. Biomedicines 12 (1) (2023)
Tatiana Markova, Natalia Alekseeva, Maria Lalayants, Oxana P Ryzhkova, Olga Mironovich, Nailya Galeeva, Elena A Bliznetz, Oleg Belov, Svetlana Chibisova, Alexander Polyakov, George Tavarkiladze
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss. Journal of personalized medicine 12 (11) (2022)
Tatiana Markova, Natalia Alekseeva, Maria Lalayants, Oxana P Ryzhkova, Olga Mironovich, Nailya Galeeva, Elena A Bliznetz, Oleg Belov, Svetlana Chibisova, Alexander Polyakov, George Tavarkiladze
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss. Journal of personalized medicine 12 (11) (2022)
Aisen V Solovyev, Alena Kushniarevich, Elena A Bliznetz, Marita Bady-Khoo, Maria R Lalayants, Tatiana G Markova, Gabriel Minárik, L'udevít Kádasi, Ene Metspalu, Vera G Pshennikova, Fedor M Teryutin, Elza K Khusnutdinova, Alexander Poliakov, Mait Metspalu, Olga L Posukh, Nikolay A Barashkov, Sardana A Fedorova
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia. Human genetics (2021)
Maria R Lalayants, Olga Mironovich, Elena A Bliznetz, Tatiana G Markova, Alexander V Polyakov, George Tavarkiladze
[OTOF-related auditory neuropathy spectrum disorder]. Vestnik otorinolaringologii 85 (2) (2020)
Tatiana G Markova, N N Alekseeva, Olga Mironovich, Elena A Bliznetz, Maria R Lalayants, Alexander V Polyakov, George Tavarkiladze
[Hearing loss due to mutations or lack of the gene coding protein stereocillin]. Vestnik otorinolaringologii 85 (2) (2020)
Polina Gundorova, Rena A Zinchenko, Irina A Kuznetsova, Elena A Bliznetz, Anna A Stepanova, Aleksander V Polyakov
Molecular-genetic causes for the high frequency of phenylketonuria in the population from the North Caucasus. PloS one 13 (8) (2018)