Get started
Author

Yuri V. Vyatkin

Observed names: Vyatkin, Yuri, Y Vyatkin, Y. V. Vyatkin, Y. Vyatkin, Y.V. Vyatkin, Yu. V Vyatkin, Yu. V. Vyatkin, Yu.V. Vyatkin, Yuri Vyatkin, Вяткин Ю. В., Ю. В. Вяткин, Ю.В. Вяткин
Observed institutions: Novosibirsk State University, Lomonosov Moscow State University, National Research Center for Preventive Medicine, Institute of Cytology and Genetics, Ministry of Health of the Russian Federation, Siberian Branch of the Russian Academy of Sciences, St. Laurent Institute
ORCID: 0000-0002-9056-8796
Observed ORCID: 0000-0002-9056-8796
OpenAlex ID: A5050455475
On the importance of small changes in RNA expression
2013 · Georges St. Laurent, Dmitry Shtokalo, et al. · Methods · 84
Deep Sequencing Transcriptome Analysis of Murine Wound Healing: Effects of a Multicomponent, Multitarget Natural Product Therapy-Tr14
2017 · Georges St. Laurent, Bernd Seilheimer, et al. · Frontiers in Molecular Biosciences · 55
PDF
Dark matter RNA illuminates the puzzle of genome-wide association studies
2014 · Georges St. Laurent, Yuri Vyatkin, et al. · BMC Medicine · 47
PDF
Identification of novel GLI1 target genes and regulatory circuits in human cancer cells
2018 · Yumei Diao, Mohammed Ferdous‐Ur Rahman, et al. · Molecular Oncology · 42
PDF
Functional annotation of the vlinc class of non-coding RNAs using systems biology approach
2016 · Georges St. Laurent, Yuri Vyatkin, et al. · Nucleic Acids Research · 42
PDF
Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region
2021 · Vasily E. Ramensky, Alexandra I. Ershova, et al. · Frontiers in Genetics · 35
Generation of induced pluripotent stem cell lines ICGi021-A and ICGi022-A from peripheral blood mononuclear cells of two healthy individuals from Siberian population
2020 · A.A. Malakhova, E.V. Grigor'eva, et al. · Stem Cell Research · 31
PDF
Very long intergenic non-coding (vlinc) RNAs directly regulate multiple genes in cis and trans
2021 · Huifen Cao, Dongyang Xu, et al. · BMC Biology · 28
PDF
Biomarker discovery in attention deficit hyperactivity disorder: RNA sequencing of whole blood in discordant twin and case-controlled cohorts
2020 · Timothy A. McCaffrey, Georges St. Laurent, et al. · BMC Medical Genomics · 23
PDF
Style transfer with variational autoencoders is a promising approach to RNA-Seq data harmonization and analysis
2020 · Nikolai Russkikh, Denis Antonets, et al. · Bioinformatics · 21
PDF
Applying Patient-Specific Induced Pluripotent Stem Cells to Create a Model of Hypertrophic Cardiomyopathy
2019 · E. V. Dementyeva, S. P. Medvedev, et al. · Biochemistry (Moscow) · 20
Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot Study
2023 · Anastasia V. Blokhina, Alexandra I. Ershova, et al. · International Journal of Molecular Sciences · 17
PDF
Genetic analysis of patients with hypertrophic cardiomyopathy
2020 · E. V Dementyeva, Yu. V Vyatkin, et al. · Genes and Cells · 16
PDF
Genetic landscape in Russian patients with familial left ventricular noncompaction
2023 · Alexey N. Meshkov, Roman P. Myasnikov, et al. · Frontiers in Cardiovascular Medicine · 15
Genome-wide profiling and differential expression of microRNA in rat pluripotent stem cells
2017 · Vladimir V. Sherstyuk, Sergey P. Medvedev, et al. · Scientific Reports · 15
PDF
The Metagenomic Analysis of Viral Diversity in Colorado Potato Beetle Public NGS Data
2023 · Maria Starchevskaya, Ekaterina Kamanova, et al. · Viruses · 13
PDF
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene
2022 · Roman Myasnikov, Anna Bukaeva, et al. · Genes · 13
PDF
Creation of Induced Pluripotent Stem Cells ICGi044-B and ICGi044-C Using Reprogramming of Peripheral Blood Mononuclear Cells of a Patient with Parkinson’s Disease Associated with c.1492T>G Mutation in the GLUD2 Gene
2023 · D. A. Sorogina, E. V. Grigor’eva, et al. · Russian Journal of Developmental Biology · 10
Generation of induced pluripotent stem cell line, ICGi034-A, by reprogramming peripheral blood mononuclear cells from a patient with Parkinson’s disease associated with GBA mutation
2021 · Elena V. Grigor'eva, Elena S. Drozdova, et al. · Stem Cell Research · 10
PDF
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases
2022 · Evgeniia A. Sotnikova, Anna V. Kiseleva, et al. · Journal of Personalized Medicine · 9
PDF
Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia
2024 · Anastasia V. Blokhina, Alexandra I. Ershova, et al. · International Journal of Molecular Sciences · 8
PDF
Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study
2024 · Anastasia V. Blokhina, Alexandra I. Ershova, et al. · PLoS ONE · 7
Validation of genetic risk scores for coronary artery disease, developed on European population samples, in Russian population
2024 · A. I. Ershova, A. N. Meshkov, et al. · CARDIOVASCULAR THERAPY AND PREVENTION · 7
PDF
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities
2024 · Anna Bukaeva, Roman Myasnikov, et al. · International Journal of Molecular Sciences · 6
Assessment of polygenic risk of hypertension
2023 · A. S. Limonova, A. I. Ershova, et al. · CARDIOVASCULAR THERAPY AND PREVENTION · 6
PDF
Works count: 78
Citation count: 657
H-index: 15
I10-index: 19
Year
Topic
Type