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Irina Zh. Zhalsanova

Observed names: I. Z. Zhalsanova, I. Zh. Zhalsanova, I. Zhalsanova, I.Zh. Zhalsanova, Irina Z. Zhalsanova, Irina Z.H. Zhalsanova, Irina Zhalsanova, Irina Zhargalovna Zhalsanova, Zhalsanova I Zh, Жалсанова Ирина Жаргаловна, И. Ж. Жалсанова, И.Ж. Жалсанова, Ирина Жаргаловна Жалсанова
ORCID: 0000-0001-6848-7749
Observed ORCID: 0000-0001-6848-7749
OpenAlex ID: A5003106718
Molecular Relationships between Bronchial Asthma and Hypertension as Comorbid Diseases
2018 · Elena Yu. Bragina, Irina A. Goncharova, et al. · Berichte aus der medizinischen Informatik und Bioinformatik/Journal of integrative bioinformatics · 20
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Genetic comorbidity of hypertension and bronchial asthma
2022 · E. Yu. Bragina, I A. Goncharova, et al. · Arterial’naya Gipertenziya (Arterial Hypertension) · 5
Modifier Genes as a Cause of Wilson–Konovalov Disease Clinical Polymorphism
2021 · A. E. Postrigan, I. Zh. Zhalsanova, et al. · Russian Journal of Genetics · 4
Effect of IL10 (rs1800872) and CXCL10 (rs4386624, rs4256246) genes polymorphism in the development of viral and bacterial infectious diseases
2019 · Irina A. Goncharova, Elena Yu. Bragina, et al. · RESEARCH RESULTS IN BIOMEDICINE · 4
Analysis of Haplotypes of Cat, Tlr4, and Il10 Genes in Bronchial Asthma Patients Comorbid With Arterial Hypertension
2019 · E. Y. Bragina, I. A. Goncharova, et al. · Сибирский научный медицинский журнал · 4
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Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI
2023 · Irina Zh. Zhalsanova, Anna Evgenievna Postrigan, et al. · International Journal of Molecular Sciences · 3
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The ATOX1 Gene Role in Copper Metabolism and the Pathogenesis of Copper-Induced Diseases
2023 · I. Zh. Zhalsanova, E. A. Fonova, et al. · Russian Journal of Genetics · 3
Case Report: Compound Heterozygous Variants of the MAN1B1 Gene in a Russian Patient with Rafiq Syndrome
2022 · Irina Zh. Zhalsanova, Ekatherina G. Ravzhaeva, et al. · International Journal of Molecular Sciences · 3
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The heterogeneity of non-motor symptoms in patients with Parkinson's disease in Tomsk region
2019 · M.A. Nikitina, N.G. Zhukova, et al. · Yakut Medical Journal · 3
The analysis of associations between cytokine network genes and inverse co-morbidity of bronchial asthma and tuberculosis
2016 · Bragina E Yu, Freidin MB, et al. · Biomedical Genetics and Genomics · 3
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Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1 Duplications
2024 · A. A. Kashevarova, M. E. Lopatkina, et al. · Molecular Genetics & Genomic Medicine · 2
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Current aspects and approaches to molecular diagnostics of hereditary neuromuscular diseases
2024 · Elizaveta A. Fonova, Irina Zh. Zhalsanova, et al. · RUDN Journal of Medicine · 2
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Bronchial asthma in the genetic framework of cardiovascular continuum syntropy
2022 · E. Yu. Bragina, I. A. Goncharova, et al. · Сибирский журнал клинической и экспериментальной медицины · 2
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The role of the TNF (rs1800629), TNFB (rs2239704) and TNFRSF1B (rs652625) genes polymorphic variants in the allergic and infectious disease's development
2020 · И.Ж. Жалсанова, Е.Ю. Брагина, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 2
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Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing
2022 · A. A. Sivtsev, I. Zh. Zhalsanova, et al. · Russian Clinical Laboratory Diagnostics · 1
Analysis of mutations spectrum in the KCNQ1, KCNH2 and SCN5A genes in patients with long QT syndrome using massively parallel sequencing
2020 · А.А. Сивцев, Л.И. Свинцова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 1
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Association of celiac disease genetic markers with reproduction disorders
2019 · L. I. Minaycheva, E. Yu. Bragina, et al. · Almanac of Clinical Medicine · 1
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The role of genes IL10 (rs1800872) and TNF (rs2239704) in the pathogenesis of bronchial asthma and tuberculosis
2018 · Irina Zhalsanova, Elena Bragina, et al. · European Respiratory Journal · 1
A novel variant of NF1 gene in a patient with neurofibromatosis type 1: a case report
2026 · I. Zh. Zhalsanova, E. A. Fonova, et al. · Siberian Journal of Oncology
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A novel homozygous variant in the ATP7B gene in a patient with Wilson’s disease: a case report
2026 · Valentina E. Shavrak, Irina Z. Zhalsanova, et al. · Frontiers in Medicine
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A familial case of Bothnian palmoplantar keratoderma caused by the c.103T>G substitution in the AQP5 gene
2025 · E.A. Fonova, I.Zh. Zhalsanova, et al. · Russian Journal of Clinical Dermatology and Venereology
A familial case of Marfan syndrome: a novel variant in the FBN1 gene
2025 · Vsevolod I. Stepanenko, Irina Z.H. Zhalsanova, et al. · RUDN Journal of Medicine
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PP275 Multi-omics of early-onset oral cancer
2025 · E. Kolegova, M. Patysheva, et al. · ESMO Open
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Case Report: a novel splice variant of SPAST gene in autosomal dominant spastic paraplegia, type 4
2025 · Irina Zh. Zhalsanova, Elizaveta A. Fonova, et al. · Vestnik Tomskogo gosudarstvennogo universiteta Biologiya
Case Report: A Novel Homozygous Variant of the CTSK Gene in Rare Pycnodysostosis
2024 · Irina Zhargalovna Zhalsanova, Elizaveta Alekseevna Fonova, et al. · International Journal of Molecular Sciences
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Works count: 38
Citation count: 64
H-index: 4
I10-index: 1
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