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A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches

Human Genetics, 2015-11, Vol.134 (11-12), p.1143-1162

2015

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Involvement of Mitochondria in Neurodegeneration in Multiple Sclerosis

Biochemistry (Moscow), 2018-07, Vol.83 (7), p.813-830

2018

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Multiplex Analysis of Serum Cytokine Profiles in Systemic Lupus Erythematosus and Multiple Sclerosis

International journal of molecular sciences, 2022-11, Vol.23 (22), p.13829

2022

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Analysis of miRNA Expression from the DLK1-DIO3 Locus in CD4+ and CD14+ Cells in Relapsing-Remitting Multiple Sclerosis

Neuroscience and behavioral physiology, 2023-05, Vol.53 (4), p.475-482

2023

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Family hyperaldosteronism type I: a clinical case and review of literature

Terapevtic̆eskii arhiv, 2018-09, Vol.90 (9), p.115

2018

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DNA Methylation Profile of CD14+ Monocytes Changes in Primary Progressive Multiple Sclerosis

Molecular biology (New York), 2023-10, Vol.57 (5), p.836-842

2023

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The levels of certain circulating microRNAs in hypertrophic cardiomyopathy are associated with echocardiographic parameters

Terapevtic̆eskii arhiv, 2023-05, Vol.95 (4), p.302

2023

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Variants of the Coagulation and Inflammation Genes Are Replicably Associated with Myocardial Infarction and Epistatically Interact in Russians

PloS one, 2015-12, Vol.10 (12), p.e0144190-e0144190

2015

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Hypertrophic Cardiomyopathy as an Oligogenic Disease: Transcriptomic Arguments

Molecular biology (New York), 2020-11, Vol.54 (6), p.840-850

2020

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A Markov Chain Monte Carlo Technique for Identification of Combinations of Allelic Variants Underlying Complex Diseases in Humans

Genetics (Austin), 2005-12, Vol.171 (4), p.2113-2121

2005

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GWAS-identified multiple sclerosis risk loci involved in immune response: Validation in Russians

Journal of neuroimmunology, 2015-05, Vol.282, p.85-91

2015

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MiRNA miR-375 as a Multifunctional Regulator of the Cardiovascular System

Molecular biology (New York), 2022-06, Vol.56 (3), p.363-371

2022

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Autophagy: Mechanisms, regulation, and its role in tumorigenesis

Biochemistry (Moscow), 2013-04, Vol.78 (4), p.355-367

2013

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Kinase mTOR: Regulation and role in maintenance of cellular homeostasis, tumor development, and aging

Biochemistry (Moscow), 2014-02, Vol.79 (2), p.88-101

2014

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Association of Polymorphic Genome Variants in the 2q32.1 Locus with the Development of Vasovagal Syncope

Molecular biology (New York), 2023-10, Vol.57 (5), p.843-847

2023

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Age-Dependent Approach to Search for Genetic Variants Associated with Myocardial Infarction

Molecular biology (New York), 2020-07, Vol.54 (4), p.618-622

2020

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Genome-Wide Analysis of DNA Methylation in Cd4+ T Lymphocytes of Patients with Primary Progressive Multiple Sclerosis Indicates Involvement of This Epigenetic Process in the Disease Immunopathogenesis

Molecular biology (New York), 2022-06, Vol.56 (3), p.417-423

2022

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Risk of Multiple Sclerosis: Analysis of Interactions between Variants of Nuclear and Mitochondrial Genomes

Molecular biology (New York), 2021-11, Vol.55 (6), p.839-846

2021

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Genetic Markers for Personalized Therapy of Polygenic Diseases: Pharmacogenetics of Multiple Sclerosis

Molecular biology (New York), 2019-07, Vol.53 (4), p.513-534

2019

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The Myocardial Infarction Associated Variant in the MIR196A2 Gene and Presumable Signaling Pathways to Involve miR-196a2 in the Pathological Phenotype

Molecular biology (New York), 2018-11, Vol.52 (6), p.872-877

2018

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Variability of the Mitochondrial Genome and Development of the Primary Progressing form of Multiple Sclerosis

Molecular biology (New York), 2020-07, Vol.54 (4), p.535-540

2020

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Circular RNAs: Biogenesis, Functions, and Role in Myocardial Hypertrophy

Biochemistry (Moscow), 2024, Vol.89 (Suppl 1), p.S1-S13

2024

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Metal-dependent hydrolysis of myelin basic protein by IgGs from the sera of patients with multiple sclerosis

Immunology Letters, 2006-02, Vol.103 (1), p.75-81

2006

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Analysis of Associations of Polymorphisms of Genes Encoding Cytokine Receptors with the Clinical Features of Multiple Sclerosis

Neuroscience and behavioral physiology, 2018-03, Vol.48 (3), p.337-341

2018

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Variability of the MIR196A2 Gene as a Risk Factor in Primary-Progressive Multiple Sclerosis Development

Molecular biology (New York), 2019-03, Vol.53 (2), p.249-255

2019

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A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches

Involvement of Mitochondria in Neurodegeneration in Multiple Sclerosis

Multiplex Analysis of Serum Cytokine Profiles in Systemic Lupus Erythematosus and Multiple Sclerosis

Analysis of miRNA Expression from the DLK1-DIO3 Locus in CD4+ and CD14+ Cells in Relapsing-Remitting Multiple Sclerosis

Family hyperaldosteronism type I: a clinical case and review of literature

DNA Methylation Profile of CD14+ Monocytes Changes in Primary Progressive Multiple Sclerosis

The levels of certain circulating microRNAs in hypertrophic cardiomyopathy are associated with echocardiographic parameters

Variants of the Coagulation and Inflammation Genes Are Replicably Associated with Myocardial Infarction and Epistatically Interact in Russians

Hypertrophic Cardiomyopathy as an Oligogenic Disease: Transcriptomic Arguments

A Markov Chain Monte Carlo Technique for Identification of Combinations of Allelic Variants Underlying Complex Diseases in Humans

GWAS-identified multiple sclerosis risk loci involved in immune response: Validation in Russians

MiRNA miR-375 as a Multifunctional Regulator of the Cardiovascular System

Autophagy: Mechanisms, regulation, and its role in tumorigenesis

Kinase mTOR: Regulation and role in maintenance of cellular homeostasis, tumor development, and aging

Association of Polymorphic Genome Variants in the 2q32.1 Locus with the Development of Vasovagal Syncope

Age-Dependent Approach to Search for Genetic Variants Associated with Myocardial Infarction

Genome-Wide Analysis of DNA Methylation in Cd4+ T Lymphocytes of Patients with Primary Progressive Multiple Sclerosis Indicates Involvement of This Epigenetic Process in the Disease Immunopathogenesis

Risk of Multiple Sclerosis: Analysis of Interactions between Variants of Nuclear and Mitochondrial Genomes

Genetic Markers for Personalized Therapy of Polygenic Diseases: Pharmacogenetics of Multiple Sclerosis

The Myocardial Infarction Associated Variant in the MIR196A2 Gene and Presumable Signaling Pathways to Involve miR-196a2 in the Pathological Phenotype

Variability of the Mitochondrial Genome and Development of the Primary Progressing form of Multiple Sclerosis

Circular RNAs: Biogenesis, Functions, and Role in Myocardial Hypertrophy

Metal-dependent hydrolysis of myelin basic protein by IgGs from the sera of patients with multiple sclerosis

Analysis of Associations of Polymorphisms of Genes Encoding Cytokine Receptors with the Clinical Features of Multiple Sclerosis

Variability of the MIR196A2 Gene as a Risk Factor in Primary-Progressive Multiple Sclerosis Development

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