Author

Natalia Doroschuk

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Research Focus:database / resource· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Mary V. WoroncowiD· 3 shared Olesya V. SagaydakiD· 3 shared Pavel VolchkoviD· 3 shared Viktor P. BogdanoviD· 3 shared Elizaveta V. SaryginaiD· 2 shared Eugene Albert· 2 shared Julia Krupinova· 2 shared Olga N. MityaevaiD· 2 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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3 shared papersGenomics

Mary V. WoroncowORCID

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Author profile →

3 papers

Recent·Most cited

HLA alleles and haplotype distribution across Russian population groups

Varvara V. Kucherenko, Natalia Doroschuk, Elizaveta V. Sarygina, Olesya V. Sagaydak, Viktor P. Bogdanov, Olga N. Mityaeva, Julia Krupinova, Mary V. Woroncow, Eugene Albert, Pavel Volchkov

This study reports HLA allele and haplotype frequencies across 14 Russian ethnic groups using whole genome sequencing data, highlighting differences in risk alleles for type 1 diabetes and improving HLA frequency coverage in eastern Europe and northern Asia.

International Journal of Molecular Sciences · Jun 3, 2026Peer-reviewedGenetics

Systematic analysis of insertions signature in gnomAD revealed large set of novel processed pseudogenes

Artem Podvalnyi, Varvara V. Kucherenko, Natalia Doroschuk, Elizaveta V. Sarygina, Olesya V. Sagaydak, Olga N. Mityaeva, Viktor P. Bogdanov, Julia Krupinova, Mary V. Woroncow, Pavel Volchkov, Eugene Albert

The paper identifies novel non-reference processed pseudogenes by analyzing insertion artifacts in gnomAD data, improving variant interpretation.

bioRxiv · Jan 15, 2026 · PreprintGenomics

Sanger validation of WGS variants - when to?

Arina Kopernik, Г.Ю. Зобкова, Natalia Doroschuk, Anna Smirnova, Daria Molodtsova-Zolotukhina, Olesya V. Sagaydak, О. П. Рыжкова, Sergey Ivanovich Kutsev, Olga S. Groznova, L. P. Melikyan, Elizaveta Bondarchuk, Mary V. Woroncow, Eugene A Albert, Viktor P. Bogdanov, Pavel Volchkov

This study evaluates concordance between whole genome sequencing variants and Sanger validation to establish thresholds for high-quality variant filtering.

bioRxiv · Apr 19, 2024 · PreprintGenomics