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Research Interests

Papers共 47 篇Author StatisticsCo-AuthorSimilar Experts

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Sanger validation of WGS variants - when to
Arina Kopernik,Gaukhar Zobkova, Natalia Doroschuk, Anna Smirnova, Daria Molodtsova-Zolotukhina,Olesya Sagaydak,Oxana Ryzhkova,Sergey Kutsev, Olga Groznova, Lyusya Melikyan, Elizaveta Bondarchuk, Mary Woroncow, Eugene Albert, Viktor Bogdanov,Pavel Volchkov
biorxiv（2024）
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A MODEL FOR ASSESSING MEDICAL EFFICACY AND COST EFFECTIVENESS OF EARLY DETECTION OF HEREDITARY CANCER USING WHOLEGENOME AND TARGETED GENETIC TESTING
Marina Kolosnitsyna,Maria Makarova, Anastasia Vladimirskaya, D.K. Chernevskiy,Olesya V. Sagaydak, M.A. Patrushev, A. S. Dorofeev
Socialʹnye aspekty zdorovʹâ naseleniâno. 5 (2023): 14-14
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The Diagnosis of Hereditary Cancer Syndromes with Atypical Manifestation: Clinical Cases
M. V. Makarova,Marina V. Nemtsova,Maxim S. Belenikin,Anastasia A. Krinitsina, D. K. Chernevskiy,Elena E. Baranova,Olesya V. Sagaydak, M. M. Byakhova, E. N. Kulikova, A. P. Chernova, А. А. Дорофеев
Zlokačestvennye opuholino. 4 (2023): 93-100
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CDKN2A Gene Mutations: Implications for Hereditary Cancer Syndromes
Anastasiia Danishevich,Airat Bilyalov,Sergey Nikolaev, Nodirbec Khalikov, Daria Isaeva, Yuliya Levina,Maria Makarova, Marina Nemtsova, Denis Chernevskiy,Olesya Sagaydak,Elena Baranova,Maria Vorontsova, Mariya Byakhova, Anna Semenova, Vsevolod Galkin,Igor Khatkov,Saida Gadzhieva,Natalia Bodunova
Biomedicinesno. 12 (2023): 3343-3343
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Early diagnosis of camurati–engelmann disease, also known as progressive diaphyseal dysplasia: detection of a causative mutation by whole genome sequencing
O.S. Kokorina, ,O.V. Sagaydak,E.E. Baranova,G.Yu. Zobkova,M.S. Belenikin, O.S. Groznova, L.P. Melikyan, O.A. Shidlovskaya, , , , , , , , , ,
Педиатрияno. 5 (2022): 168-172
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Author Statistics

#Papers: 47

#Citation: 203

H-Index: 4

G-Index: 14

Sociability: 5

Diversity: 2

Activity: 3

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