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Renata R. Savchenko

Observed names: R. R. Savchenko, R.R. Savchenko, Renata Savchenko, Savchenko, R.R., Savchenko, Renata, Р. Р. Савченко, Р.Р. Савченко, Рената Ренатовна Савченко
ORCID: 0000-0003-3839-3543
Observed ORCID: 0000-0003-3839-3543
OpenAlex ID: A5061287876
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22
2018 · Anna A. Kashevarova, Elena O. Belyaeva, et al. · Molecular Cytogenetics · 17
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Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay
2021 · Stanislav A. Vasilyev, Nikolay A. Skryabin, et al. · Cytogenetic and Genome Research · 14
Effect of Fluoxetine on Neurogenesis in Hippocampal Dentate Gyrus after Global Transient Cerebral Ischemia in Rats
2016 · M. Yu. Khodanovich, A. A. Kisel’, et al. · Bulletin of Experimental Biology and Medicine · 12
FISH Diagnostics of Chromosomal Translocation with the Technology of Synthesis of Locus-Specific DNA Probes Based on Long-Range PCR
2020 · D. I. Zhigalina, N. A. Skryabin, et al. · Russian Journal of Genetics · 8
Transcription factor TCF4: structure, function, and associated diseases
2024 · R. R. Savchenko, N. A. Skryabin · Vavilov Journal of Genetics and Breeding · 5
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Ontogenetic Pleiotropy of Genes Involved in CNVs in Human Spontaneous Abortions
2019 · A. A. Kashevarova, N. A. Skryabin, et al. · Russian Journal of Genetics · 4
Osteoinductive Properties of Secretome of Human Mesenchymal Stem Cells, Obtained with Automatic Cell Culture System
2020 · S. A. Aleksandrova, Yu. A. Nashchekina, et al. · Cell and Tissue Biology · 3
Hippocampal neurogenesis in the new model of global cerebral ischemia
2015 · A. A. Kisel, G. A. Chernysheva, et al. · AIP conference proceedings · 3
Анализ CNVs при анэмбрионии и неразвивающейся беременности
2018 · Р. Р. Савченко, А. А. Кашеварова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 2
Dark side of glial talk: Role of neuroinflammation in neurodegeneration
2026 · Alexandr D. Okhalnikov, Renata Savchenko, et al. · Neural Regeneration Research · 1
Functional analysis of a new splicing mutation in the MYBPC3 gene in hypertrophic cardiomyopathy
2024 · R. R. Salakhov, M. V. Golubenko, et al. · Bulletin of Siberian Medicine · 1
Effect of ADAMTS1 Differential Expression on the Radiation-Induced Response of HеLа Cell Line
2021 · R. R. Savchenko, A. A. Murashkina, et al. · Russian Journal of Genetics · 1
Runs of homozygosity in spontaneous abortions from families with recurrent pregnancy loss
2019 · N. A. Skryabin, S. A. Vasilyev, et al. · Vavilov Journal of Genetics and Breeding · 1
Онтогенетическая плейотропия генов, вовлеченных в CNV у спонтанных абортусов человека
2019 · А. А. Кашеварова, Н. А. Скрябин, et al. · Генетика · 1
Microarray Analysis of Differential Expression of Long Non-coding RNAs in Peripheral Blood Mononuclear Cells in Luminal A Breast Cancer
2025 · Varvara I. Minina, Ruslan A. Titov, et al. · Gene Expression
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Microarray Analysis of the Transcriptome of Peripheral Blood Lymphocytes in Breast Cancer Patients
2025 · V. I. Minina, R. A. Titov, et al. · Russian Journal of Genetics
Generation of an Induced Pluripotent Stem Cell Line TNRMCi001-A by Reprogramming Fibroblasts from a Homozygous F508del Cystic Fibrosis Patient
2023 · D. I. Zhigalina, T. N. Kireeva, et al. · Russian Journal of Developmental Biology
ADAMTS1 Is Differentially Expressed in Human Lymphocytes with Various Frequencies of Endogenous γH2AX Foci and Radiation-Induced Micronuclei
2022 · S. A. Vasilyev, R. R. Savchenko, et al. · Russian Journal of Genetics
Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene
2021 · D.I. Zhigalina, A.A. Malakhova, et al. · Stem Cell Research
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Влияние дифференциальной экспрессии гена ADAMTS1 на радиационно-индуцированный ответ клеточной линии HеLа
2021 · Р. Р. Савченко, А. А. Мурашкина, et al. · Генетика
Supplementary Material for: Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay
2021 · Vasilyev, S.A., Skryabin, N.A., et al. · Figshare
The effect of ADAMTS1, RBFOX2, THBS1 and WHSC1 gene expression on the formation of a radiation-induced cellular response
2020 · Р.Р. Савченко, С.А. Васильев, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
Effect of the THBS1 Gene Knockout on the Radiation-Induced Cellular Response in a Model System In Vitro
2020 · R. R. Savchenko, S. A. Vasilyev, et al. · Russian Journal of Genetics
Влияние нокаута гена THBS1 на формирование радиационно-индуцированного клеточного ответа в модельной системе in vitro
2020 · Р. Р. Савченко, С. А. Васильев, et al. · Генетика
Osteoinductive Properties of PLGA/HA/β-TCP Composite Polymer Scaffolds
2019 · Svetlana Aleksandrova, Liubov Pokrovskaya, et al. · Proceedings of the World Congress on Electrical Engineering and Computer Systems and Science
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Works count: 30
Citation count: 72
H-index: 5
I10-index: 3
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