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Н. В. Кох

Observed names: N V Kokh, N. Kokh, N. V. Kokh, N.V. Kokh, N.V. Kokh Kokh, Natalia Kokh, Natalia Viktorovna Kokh, NataliaV. Kokh, Nataly V. Kokh, Кох Н. В., Кох Наталья Викторовна, Н. Кох, Наталья Владимировна Кох
ORCID: 0000-0001-6374-1728
Observed ORCID: 0000-0001-6374-1728
OpenAlex ID: A5012574099
Introduction of modern genetic and instrumental examination methods in patients with ichthyosis vulgaris and atopic dermatitis
2023 · A.A. Eremina, A.V. Gerlinger, et al. · Russian Journal of Clinical Dermatology and Venereology · 7
Association of environmental factors with overweight and obesity in preschool and primary school children
2021 · E. V. Shrayner, N. V. Kokh, et al. · Сибирский журнал клинической и экспериментальной медицины · 7
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Identification of ethnogenetic differences in genetic markers in the clinical course and damage to target organs in arterial hypertension in Russians and Buryats
2020 · A. Kovaleva, N. Kokh, et al. · Patologiya krovoobrashcheniya i kardiokhirurgiya · 7
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The relationship of genetic risk factors with the development of arterial hypertension taking into account ethnic differences
2019 · A. Ya. Kovaleva, N. V. Kokh, et al. · Russian Journal of Cardiology · 7
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Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants
2025 · Maria Gridina, Timofey Lagunov, et al. · Genome Medicine · 6
Быстрые Темпы Насыщения Варфарином—предиктор Развития Чрезмерной Гипокоагуляции. Модернизация Алгоритма Подбора Дозы Варфарина
2015 · Е. С. Кропачева, Н. Н. Боровков, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 5
Personalized approach of medication by indirect anticoagulants tailored to the patient—Russian context: what are the prospects?
2012 · Liliya Alexandrovna Belozerceva, Elena Nikolaevna Voronina, et al. · The EPMA Journal · 5
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A HGF Mutation in the Familial Case of Primary Lymphedema: A Report
2024 · Galina Koksharova, Natalia Kokh, et al. · International Journal of Molecular Sciences · 3
Association of genetic prerequisites of vitamin D deficiency with severity of past COVID-19 infection
2022 · E. V. Shrayner, S. K. Petukhova, et al. · Экспериментальная и клиническая гастроэнтерология · 3
Clinical significance of studying the genetic polymorphism of adhesion factors in Helicobacter pylori-associated diseases
2022 · G. I. Lifshits, E. V. Shrayner, et al. · Экспериментальная и клиническая гастроэнтерология · 3
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Clinical cases of patients homozygous for the 2282del4 (rs558269137) mutation in the filaggrin gene
2022 · O.A. Makeenko, N.V. Kokh, et al. · Russian Journal of Clinical Dermatology and Venereology · 3
Relationship between cholelithiasis and metabolic syndrome: the role of genetic factors
2022 · Maria S. Novikova, Evgenia V. Shrayner, et al. · Экспериментальная и клиническая гастроэнтерология · 2
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Filaggrin gene mutations and cytokine genes polymorphism in siblings with atopic dermatitis
2021 · M.S. Novikova, N.V. Kokh, et al. · Russian Journal of Clinical Dermatology and Venereology · 2
Clinical presentation of patients with a mutation in the filaggrin gene at the dermatologist’s office
2022 · O.A. Makeenko, N.V. Kokh, et al. · Russian Journal of Clinical Dermatology and Venereology · 1
Study of the FUT2 gene association with infection and clinical manifestations of Helicobacter pylori infection
2021 · A. S. Klimova, E. V. Shrayner, et al. · Экспериментальная и клиническая гастроэнтерология · 1
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Study of association of the rs5400 polymorphic locus in the SLC2A2 (GLUT2) gene and the rs4684677 polymorphic locus in the GHRL gene with excess body weight and preference for carbohydrates in preschool and primary school-aged children
2021 · N. V. Kokh, E. V. Schreiner, et al. · Russian Pediatric Journal · 1
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Genetic risk factors of cytolysis syndrome in the treatment of recrudescence of chronic cardiovascular diseases
2018 · N. V. Kokh, E. N. Voronina, et al. · Russian Journal of Cardiology · 1
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Nutriogenetic Test in Clinical Practice: Goals and Opportunities
2017 · E M Zelenskaya, N V Kokh, et al. · Journal of clinical practice · 1
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Approaches to Prevention and Treatment of Metabolic Syndrome: Nutrigenetics
2017 · N.V. Kokh, A.A. Slepukhina, et al. · Siberian medical review · 1
Comparison of Empiric and Pharmacogenetic Approaches in Assessment of Efficacy of Anticoagulant Therapy
2015 · N.V. Kokh Kokh, A.A. Slepukhina Slepukhina, et al. · Kardiologiia · 1
Фолатный цикл: обзор и практические рекомендации по интерпретации генетических тестов
2015 · Н. В. Кох, А. А. Слепухина, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 1
Comparative characteristics of patients with follicular occlusion syndrome and severe acne
2026 · A.A. Yeremina, N.V. Kokh, et al. · Russian Journal of Clinical Dermatology and Venereology
Nucleotide sequence variants in IL4 and TNFA genes in patients with dermatoses and xerosis
2025 · O.A. Makeenko, A.A. Eremina, et al. · Russian Journal of Clinical Dermatology and Venereology
Assessment of the contribution of UGT1A gene polymorphisms to the development of cholelithiasis
2024 · E. V. Shreiner, A. I. Khavkin, et al. · Экспериментальная и клиническая гастроэнтерология
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Benefits of NGS for Genetic Testing of Primary Lymphedema
2023 · NataliaV. Kokh, Koksharova Galina Sergeevna, et al. · IEEE Ural-Siberian Conference on Computational Technologies in Cognitive Science, Genomics and Biomedicine (CSGB)
Works count: 43
Citation count: 68
H-index: 5
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