Vitaly V Kadyshev

21PUBLICATIONS
67CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene mappingCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Optical technology
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Publications (21)

|Oct 27, 2026
Whole-Genome Sequencing in Diagnostics of Unsolved Cases of Inherited Retinal Diseases.

|Jul 15, 2026
Bayesian Population-Based Prevalence Estimation of KCNV2-Associated Retinopathy: A Comparative Analysis of Disease-Associated Variant Frequencies in Russian and Global Populations.

|Jun 26, 2026
Clinical and Genetic Characterization of a Russian Family with Bardet-Biedl Syndrome Carrying a Previously Undescribed Missense Variant and a Recurrent Pathogenic Frameshift Variant in BBS7 Gene.

|Mar 18, 2026
[Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 2. Clinical, social and demographic characteristics of inherited retinal pathologies].

V V Kadyshev, A A Stepanova, K K Shefer

|Mar 18, 2026
[Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 1. Molecular genetic characteristics of inherited retinal pathologies].

V V Kadyshev, A A Stepanova, K K Shefer

|Apr 28, 2025
Expanding the Clinical Spectrum of BCARD Syndrome Caused by Novel Biallelic Variants in the PLOD3 Gene.

Evgeniya Melnik, Tatiana Markova, Yana Fedotova

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Frequent Collaborators

11 joint publications

Rena Zinchenko

9 joint publications

Andrey V Marakhonov

8 joint publications

Olga Shchagina

8 joint publications

Anna Stepanova