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Denis K. Chernevskiy

Observed names: D. K. Chernevskii, D. K. Chernevskiy, D. K. Chernevsky, D.K. Chernevskiy, D.  K. Chernevskiy, DK Chernevskiy, Denis Chernevskiy, Denis Konstantinovich Chernevskiy, Д. К. Черневский, Денис Константинович Черневский, Черневский Д.К., Черневский, Денис
ORCID: 0000-0002-9734-017X
Observed ORCID: 0000-0002-9734-017X
OpenAlex ID: A5035376587
CDKN2A Gene Mutations: Implications for Hereditary Cancer Syndromes
2023 · Anastasiia Danishevich, Airat Bilyalov, et al. · Biomedicines · 31
Variation of Genomic Sites Associated with Severe Covid-19 Across Populations: Global and National Patterns
2021 · Oleg Balanovsky, Valeria Petrushenko, et al. · Pharmacogenomics and Personalized Medicine · 21
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Cartographic atlas of frequency variation for 45 pharmacogenetic markers in populations of Russia and its neighbor states
2020 · EV Balanovska, VS Petrushenko, et al. · Bulletin of Russian State Medical University · 16
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Genogeografiya v Rossii i mire SNP-markerov gena LZTFL1, associirovannyh s tyazhelym techeniem COVID-19
2022 · EV Balanovska, IO Gorin, et al. · Bulletin of Russian State Medical University · 10
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Gene pool of the Novgorod population: Between the north and the south
2017 · E. V. Balanovska, A. T. Agdzhoyan, et al. · Russian Journal of Genetics · 9
The CFTR Gene Germline Heterozygous Pathogenic Variants in Russian Patients with Malignant Neoplasms and Healthy Carriers: 11,800 WGS Results
2023 · Maria Makarova, Marina Nemtsova, et al. · International Journal of Molecular Sciences · 7
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Capabilities of Molecular Genetic Methods for Effective Hereditary Cancers Detection in Individuals with High Cancer Risk Factors
2023 · Anna B. Semenova, Mariya M. Byakhova, et al. · City Healthcare · 3
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Gene Pools of Udmurts and Besermyans in the Context of Finno-ugric and Other Neighboring Ethnic Groups: the Genome-wide and Pharmacogenetic Data
2022 · Elena Vladimirovna Balanovska, Vladimir Vladimirovich Napolskikh, et al. · Ежегодник финно-угорских исследований · 3
ГЕНОФОНД НОВГОРОДЦЕВ: МЕЖДУ СЕВЕРОМ И ЮГОМ, "Генетика"
2017 · Е.В. Балановская, А.Т. Агджоян, et al. · Генетика · 3
Medical genetic counseling for patients with identified clinically significant genetic variants associated with hereditary tumor syndromes and their relatives
2023 · M.V, Makarova, M.V. Nemcova, et al. · 1
The diagnosis of hereditary cancer syndromes with atypical manifestation: clinical cases
2023 · M.  V. Makarova, M.  V. Nemtsova, et al. · Malignant tumours · 1
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The structure of pathogenic germline variants in colorectal cancer in Moscow patients
2023 · A.B. Semenova, M.M. Byakhova, et al. · Russian Journal of Archive of Pathology · 1
Breast cancer as part of Cowden syndrome
2022 · M.  M. Byakhova, A.  B. Semenova, et al. · Malignant tumours · 1
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Challenges in the differential diagnosis of 1p36 deletion syndrome and Prader–Willi syndrome
2026 · N. A. Chernevskay, O. D. Elshina, et al. · Zabajkalʹskij medicinskij vestnik
Clinical and genetic characteristics of pediatric patients with suspected hereditary liver diseases: an algorithm for differential diagnosis
2024 · D.K. Chernevskiy, A.E. Lavrova, et al. · PEDIATRIA Journal named after G N SPERANSKY
Wilson’s Disease Caused by Previously Undescribed Homozygous Nucleotide Variant of the ATP7B Gene: Clinical Cases
2024 · Denis K. Chernevskiy, Alla E. Lavrova, et al. · Вопросы современной педиатрии
Hereditary predisposition syndromes to myeloid neoplasms: diseases, genes and mechanisms of development
2024 · M. V. Makarova, M. V. Nemtsova, et al. · Oncohematology
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Особенности валидации герминальных вариантов в гене PMS2 у пациентов с наследственными опухолевыми синдромами
2024 · Ревкова М.А., Криницина А.А., et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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Possibilities of Molecular Genetic Testing of Tumor Tissue for Personalized Breast Cancer Treatment
2023 · Мария Владимировна Макарова, Марина Вячеславовна Немцова, et al. · Voprosy Onkologii
Применение расширенной NGS-панели для подбора персонализированной лекарственной терапии при метастатическом колоректальном раке: клинический случай
2023 · М. А. Ревкова, М. В. Макарова, et al. · Pharmacogenetics and Pharmacogenomics
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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
2023 · Marina Kolosnitsyna, Maria Makarova, et al. · Social Aspects of Population Health
Level of awareness as the main cause of ethical problems in genetic studies
2022 · D.K. Chernevskiy, E.A. Rozova, et al. · Neonatology News Opinions Training
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Своеобразие Новгородского генофонда в контексте народонаселения европейской части России
2021 · Балановская, Елена, Черневский, Денис, et al.
Works count: 23
Citation count: 107
H-index: 6
I10-index: 4
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