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Mikhail А. Fedyakov

Observed names: Michael Fedyakov, Mikhail A. Fedyakov, Mikhail Fedyakov, М. А. Федяков, М.А. Федяков
ORCID: 0000-0002-3291-3811
Observed ORCID: 0000-0002-3291-3811
OpenAlex ID: A5001787554
Analysis of the Spectrum of ACE2 Variation Suggests a Possible Influence of Rare and Common Variants on Susceptibility to COVID-19 and Severity of Outcome
2020 · Anton E. Shikov, Yury A. Barbitoff, et al. · Frontiers in Genetics · 41
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Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes
2019 · Oleg Glotov, Elena Serebryakova, et al. · Molecular Medicine Reports · 36
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Whole‐exome sequencing provides insights into monogenic disease prevalence in Northwest Russia
2019 · Yury A. Barbitoff, Rostislav K. Skitchenko, et al. · Molecular Genetics & Genomic Medicine · 33
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Identification of novel variants in the LDLR gene in Russian patients with familial hypercholesterolemia using targeted sequencing
2020 · Valentina Miroshnikova, Olga Romanova, et al. · Biomedical Reports · 26
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The spectrum of pathogenic variants of the ATP7B gene in Wilson disease in the Russian Federation
2019 · Mariya S. Balashova, Inna G. Tuluzanovskaya, et al. · Journal of Trace Elements in Medicine and Biology · 22
Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population
2022 · Oleg S. Glotov, Kirill V. Savostyanov, et al. · International Journal of Molecular Sciences · 15
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X-linked and autosomal dominant forms of the ichthyosis in coinheritance
2019 · Diana A. Alaverdian, Mikhail Fedyakov, et al. · Drug Metabolism and Personalized Therapy · 6
Personalized medicine: the role of sequencing technologies in diagnostics, prediction and selection of treatment of monogenous and multifactorial diseases
2022 · Oleg Glotov, Alexandr Chernov, et al. · Biological Communications · 2
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The Incidence of Lysosomal Acid Lipase Deficiency in the Russian Population
2018 · Mikhail А. Fedyakov, Yuriy А. Barbitov, et al. · Педиатрическая фармакология · 2
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The application of Nanopore sequencing for variant calling on the human mitochondrial DNA
2021 · Anton Shikov, Viktoriya Tsay, et al. · Biological Communications · 1
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The Effect of Pathogenic Tumor Suppressor Gene Variants on COVID-19: A Report of Three Cases with Varied Severity and Outcomes
2023 · Rostislav K. Skitchenko, Yury A. Barbitoff, et al. · Preprints.org
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Genetics in Ophthalmology
2020 · А.Ю. Рудник, М.А. Федяков, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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Application of NGS to improve the effectiveness of molecular genetic diagnostics of monogenic forms of diabetes in children
2020 · О.С. Глотов, Е.А. Серебрякова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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More on differential diagnosis of demyelinating and hereditary diseases
2020 · А.С. Агафьина, А.Ю. Рудник, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
Аритмогенная Кардиомиопатия/дисплазия Правого Желудочка: Клинические И Молекулярно-генетические Особенности
2015 · М. А. Федяков, О. Е. Велеславова, et al. · Journal of Arrhythmology
Works count: 15
Citation count: 184
H-index: 6
I10-index: 6
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