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Aliy Yu. Asanov

Observed names: A Yu Asanov, A. Asanov, A. Y. Asanov, A. Yu. Asanov, A.Y. Asanov, A.Y. Asanov Asanov, A.Yu. Asanov, A.Yu. Asanov Asanov, Aliy Asanov, Aliy Y. Asanov, А.Yu. А.Yu.Asanov
ORCID: 0000-0002-5388-8133
Observed ORCID: 0000-0002-5388-8133
OpenAlex ID: A5038353263
Skin DNA methylation profile in atopic dermatitis patients: A case–control study
2019 · Olga Yu. Olisova, Nikolay G. Kochergin, et al. · Experimental Dermatology · 26
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 · 19
The prevalence of Fabry disease among 1009 unrelated patients with hypertrophic cardiomyopathy: a Russian nationwide screening program using NGS technology
2022 · K. Savostyanov, A. Pushkov, et al. · Orphanet Journal of Rare Diseases · 15
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Prevalence and descriptive epidemiology of esophageal atresia in the Russian Federation
2016 · Nataliya S. Demikova, Yulia V. Vydrych, et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 15
Association of CASR, CALCR, and ORAI1 Genes Polymorphisms With the Calcium Urolithiasis Development in Russian Population
2021 · Maria M. Litvinova, Kamil Khafizov, et al. · Frontiers in Genetics · 12
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Trisomy 21 (down Syndrome) Incidence Dynamics in the Regions of the Russian Federation in 2011–2017
2019 · N.S. Demikova, M.A. Podolnaya, et al. · PEDIATRIA Journal named after G N SPERANSKY · 12
Model of Moderate Hyperhomocisteinemia Associated with Mechanical Injury: Dynamics of Morphometric Parameters of Microcirculatory Vessels
2019 · Yu. I. Pigolkin, D. B. Nikityuk, et al. · Bulletin of Experimental Biology and Medicine · 8
Genotype–Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants
2023 · Kirill Savostyanov, Alexander Pushkov, et al. · Genes · 5
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Genetic factors of the development of chronic pancreatitis
2018 · М.М. Litvinova, K.F. Khafizov, et al. · Voprosy praktičeskoj pediatrii · 5
Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters
2024 · Maria Amosova, Irina Poluboyarinova, et al. · JCEM Case Reports · 4
Ribosomal DNA Abundance in the Patient’s Genome as a Feasible Marker in Differential Diagnostics of Autism and Childhood-Onset Schizophrenia
2022 · Elizaveta Ershova, Natalia Veiko, et al. · Journal of Personalized Medicine · 4
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Genetic and Clinical Features of Shwachman-Diamond Syndrome in Russian Population: Prospective Study
2020 · Maria G. Ipatova, Ekaterina A. Deordieva, et al. · Вопросы современной педиатрии · 4
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Genetic and Clinical Features of Schimke Immuno-Osseous Dysplasia: Single-Centre Retrospective Study of 21 Unrelated Paediatric Patients over a Period of 20 Years
2025 · Anastasiia Milovanova, Petr Ananin, et al. · International Journal of Molecular Sciences · 3
Psychological rehabilitation of medical workers with emotional burnout syndrome
2019 · E. E. Achkasov, A. I. Melnikov, et al. · Russian Journal of Occupational Health and Industrial Ecology · 3
Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder
2020 · T.V. Filippova Filippova, D.V. Svetlichnaya Svetlichnaya, et al. · Urologiia · 2
Combination of multiple sclerosis and neurofibromatosis type I, remained undiagnosed from early childhood
2019 · O.N. Voskresenskaya, T.E. Shmidt, et al. · Voprosy praktičeskoj pediatrii · 2
Genetic factors for monogenic forms of calcium urolithiasis
2018 · T.V. Filippova Filippova, M.M. Litvinova Litvinova, et al. · Urologiia · 2
GC-Reach DNA Fragments Reduce the Expression of Survival Genes in MCF7 Breast Carcinoma Cells: TLR9/MyD88/NF-κB Signaling Pathway as a Potential Target for Cancer Therapy
2025 · E. M. Malinovskaya, G. V. Shmarina, et al. · Bulletin of Experimental Biology and Medicine · 1
Geno-phenotypic features of cystic fibrosis in Russian children from the Chechen and Karachay-Cherkess Republics
2024 · Maxim V. Simonov, Yulia V. Gorinova, et al. · RESEARCH RESULTS IN BIOMEDICINE · 1
Calcium-sensing receptor gene polymorphisms and their effect on response to cinacalcet treatment in patients with secondary hyperparathyroidism in chronic kidney diseases
2020 · Lilit Egshatyan, Tamara Filippova, et al. · Endocrine Abstracts · 1
DNA methylation profile in the skin of patients with atopic dermatitis
2019 · N.G. Kochergin, L.N. Kayumova, et al. · Voprosy praktičeskoj pediatrii · 1
Wilson's disease: intrafamilial clinical polymorphism
2017 · I.G. Tuluzanovskaya, N.A. Zhuchenko, et al. · PEDIATRIA Journal named after G N SPERANSKY · 1
GC-reach DNA fragments reduce survival genes expression in MCF7 cells knocked out by the TLR9 gene: TLR9/MYD88/NF-κB signaling as a potential target for cancer therapy
2024 · E. M. Malinovskaya, G. V. Shmarina, et al. · Bulletin of Experimental Biology and Medicine
Epidemiology of omphalocele: data analysis of regional congenital malformation registers in the Russian Federation
2021 · N.S. Demikova, M.A. Podolnaya, et al. · Voprosy ginekologii akušerstva i perinatologii
Lynch syndrome associated with a MLH1 gene mutation: preventive and personalized monitoring based on the results of molecular testing
2019 · M.M. Litvinova, T.S. Lisitsa, et al. · Voprosy praktičeskoj pediatrii
Works count: 31
Citation count: 146
H-index: 7
I10-index: 6
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