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Alena P. Mikhalenka

Observed names: A. Mikhalenka, A. P. Mikhalenka, A. P. Mikhalenko, A. P. Mikhalenkа, A. P. Mikhalenkо, A.P. Mikhalenka, A.  P. Mikhalenka, ALENA P. MIKHALENKA, Alena Mikhalenka, Alena Petrovna Mikhalenko
ORCID: 0000-0003-4543-2862
Observed ORCID: 0000-0003-4543-2862
OpenAlex ID: A5076449099
Genetic aspects of congenital anomalies of the kidney and urinary tract
2020 · A. V. Sukalo, A. V. Kilchevsky, et al. · Nephrology (Saint-Petersburg) · 5
Genetic polymorphism of SP-B and SP-C surfactant proteins in preterm infants with respiratory complications
2022 · V. M. Malyshava, A. P. Mikhalenka, et al. · Doklady of the National Academy of Sciences of Belarus · 4
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Association of Polymorphic Variants of VEGF and KDR Genes with Development and Metastasing of Non-Small Cell Lung Cancer
2018 · А. N. Shchayuk, E. V. Krupnova, et al. · Journal of Cancer Therapy · 3
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Prognostic Significance of Comparison of Clinical Indicators with Manifestations of Genetic Polymorphism of Glutathione-S-Transferases in Non-Small Cell Lung Cancer
2018 · Mikhail N. Shapetska, Evelina V. Krupnova, et al. · Journal of Cancer Therapy · 3
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Studying the Gut Microbiome in People Over 60
2022 · I. N. Andreeva, R. S. Shulinski, et al. · Молекулярная и прикладная генетика · 2
Determining the methylation status of the promoter regions of MARCH11, HOXA9, PTGDR, and UNCX genes in patients with non-small cell lung cancer
2023 · A. P. Mikhalenka, A. N. Shchayuk, et al. · Doklady of the National Academy of Sciences of Belarus · 1
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Germline mutations in patients with oral mucosal leukoplakia and squamous cell carcinoma: a prospective observational study
2023 · N. A. Karpuk, S. P. Rubnikovich, et al. · Кубанский научный медицинский вестник · 1
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Analysis of the function of the genes with the highest number of germinal mutations in patients with leukoplakia and cancer of the oral mucosa
2023 · Natalia Anatolievna Karpuk, Sergey Rubnikovich, et al. · Medical news of the North Caucasus · 1
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A Clinical Case of Congenital Alveolar Capillary Dysplasia: Use of High Throughput Sequencing to Verify a Diagnosis
2022 · A. P. Mikhalenka, V. M. Malyshava, et al. · Молекулярная и прикладная генетика · 1
A Range of Mutations in Patients With Isolated and Syndromal Forms of Congenital Anomalies of the Kidney and Urinary Tract
2022 · A. Ch. Mazur, A. P. Mikhalenkа, et al. · Молекулярная и прикладная генетика · 1
Polymorphisms of Drug-metabolizing Enzymes Cyp1a2, Cyp2d6, Gst, Nat2 and Transporter Mdr1 in Population of Belarus: Comparison With Selected European and Asian Populations
2016 · Alena Mikhalenka, Natalia Chebotareva, et al. · EUREKA Life Sciences · 1
Sialidosis Type II in Siblings with a Novel NEU1 Variant: Clinical and Molecular Genetic Analysis
2026 · Oksana Ch Mazur, Sergey V. Baiko, et al. · SN Comprehensive Clinical Medicine
The role of molecular genetic markers in the development of comorbid diseases in premature infants
2026 · A. P. Mikhalenka, A. P. Sukharava, et al. · Proceedings of the National Academy of Sciences of Belarus Medical series
The role of intragenic and intergenic combinations of SFTPB and SFTPC gene polymorphisms in the pathogenesis of respiratory distress syndrome and bronchopulmonary dysplasia in preterm newborns
2025 · V. M. Malyshava, A. P. Mikhalenka, et al. · Doklady of the National Academy of Sciences of Belarus
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Congenital Defects of the Immune System as a Manifestation of Monogenic Inflammatory Bowel Disease in Children
2024 · L. I. Kastsiukevich, O. N. Romanova, et al. · Hepatology and Gastroenterology
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Effect of VEGF gene polymorphism on the survival of a patient with non-small cell lung cancer
2024 · M. N. Shapetska, A. P. Mikhalenka, et al. · Doklady of the National Academy of Sciences of Belarus
Assessing the Biodiversity of the Microbiome of Endoscopically Healthy and Inflammatory Colonic Mucosa in Children With Inflammatory Bowel Disease
2024 · A.V. Gorbach, A.P. Mikhalenka, et al.
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Analysis of the relationship of somatic mutations with the development of leukoplakia and squamous cell carcinoma of the oral mucosa
2023 · N. A. Karpuk, S. P. Rubnikovich, et al. · Proceedings of the National Academy of Sciences of Belarus Medical series
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Clinical Significance of Pathogenicity of Somatic Mutations in Oral Leukoplakia: a Prospective Observational Study
2023 · N. A. Karpuk, S. P. Rubnikovich, et al. · Кубанский научный медицинский вестник
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Somatic Mutations in Patients With Leukoplakia of the Oral Mucosa
2023 · NATALIA A. KARPUK, SERGEY P. RUBNIKOVICH, et al. · The Bulletin of Contemporary Clinical Medicine
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Study of Genetic Polymorphism of Dna Methyltransferase Dnmt3b in the Patients With Nonsmall Cell Lung Cancer
2022 · A. P. Mikhalenka, А. N. Shchayuk, et al. · Молекулярная и прикладная генетика
ABCA3 gene mutations in 2 premature infants with respiratory distress syndrome
2021 · Alena Mikhalenka, V.M. Malyshava, et al. · XIth International Congress of Geneticists and Breeders from the Republic of Moldova
CYP19A1 and СOMT polymorphisms in elderly people and long-livers of Belarus
2021 · V.Y. Vinnikava, Alena Mikhalenka, et al. · XIth International Congress of Geneticists and Breeders from the Republic of Moldova
Analysis of clinically significant mutations in non-small cell lung cancer tumors
2021 · Alena Mikhalenka, A.N. Shchayuk, et al. · XIth International Congress of Geneticists and Breeders from the Republic of Moldova
The role of genetic disorders in the formation of disabling effects in the premature newborn
2020 · V. M. Malyshava, A. P. Mikhalenka, et al. · Proceedings of the National Academy of Sciences of Belarus Biological Series
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Works count: 32
Citation count: 23
H-index: 3
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