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Ilya V. Volodin

Observed names: I. V. Volodin, I. Volodin, I.V. Volodin, Ilya Volodin, Volodin, Ilya V., И.В. Володин
ORCID: 0000-0001-6539-3763
Observed ORCID: 0000-0001-6539-3763
OpenAlex ID: A5076458679
DNA methylation markers panel can improve prediction of response to neoadjuvant chemotherapy in luminal B breast cancer
2020 · Vladimir O. Sigin, Alexey I. Kalinkin, et al. · Scientific Reports · 47
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Association of oxidative stress-related genes with idiopathic recurrent miscarriage
2014 · M. B. Khadzhieva, N. N. Lutcenko, et al. · Free Radical Research · 35
Fibulin-5 (FBLN5) gene polymorphism is associated with pelvic organ prolapse
2014 · Maryam B. Khadzhieva, Svetlana V. Kamoeva, et al. · Maturitas · 33
Genetic screening of Russian Usher syndrome patients toward selection for gene therapy
2018 · Marianna E. Ivanova, Vladimir N. Trubilin, et al. · Ophthalmic Genetics · 18
New Pharmacogenetic Markers to Predict the Risk of Bleeding During Taking of Direct Oral Anticoagulants
2020 · K. B. Mirzaev, D. V. Ivashchenko, et al. · Rational Pharmacotherapy in Cardiology · 6
Mosaic Form of von Hippel–Lindau Syndrome: Case Report and Literature Review
2025 · Dmitry S. Mikhaylenko, Natalya B. Kuryakova, et al. · International Journal of Molecular Sciences · 3
Делеция импринтированного региона 14q32.2 у пациента с синдромом Кагами-Огата
2018 · Natalia Semenova, И. В. Анисимова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 2
Patients with Papillary Renal Cancer and Germline Duplication of MET Exons 5-21
2025 · Dmitry S. Mikhaylenko, Natalya B. Kuryakova, et al. · Biomedicines · 1
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Pediatric chordoma associated with tuberous sclerosis complex: A rare case report with a thorough analysis of potential therapeutic molecular targets
2022 · Kirill Anoshkin, Denis Zosen, et al. · Heliyon · 1
Initial Experience in Estimating Tumor Mutation Burden in Pediatric Hepatocellular Carcinoma
2021 · D.G. Akhaladze, G.S. Rabaev, et al. · PEDIATRIA Journal named after G N SPERANSKY · 1
Diagnostic Yield and Variant Spectrum in 375 Patients with Segmental Overgrowth and Vascular Malformations: Implications for Panel Design and Molecular Testing Strategies
2026 · Ekaterina V. Bychkova, Natalia A. Semenova, et al. · International Journal of Molecular Sciences
DNA Methylation at a Single Locus of Human Genome Accurately Recapitulates Episignature of CREBBP-Related Rubinstein–Taybi Syndrome
2025 · Olga A. Zemlianaia, Alexey I. Kalinkin, et al. · International Journal of Molecular Sciences
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Патология генов гистоновых лизин-метилтрансфераз и характерные эписигнатуры
2024 · О.А. Земляная, А.В. Ефремова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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93P IRF4 gene promoter methylation predicts efficacy of luminal B breast tumours neoadjuvant chemotherapy
2020 · V. Sigin, A.I. Kalinkin, et al. · Annals of Oncology
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Usher syndrome gene mutation spectrum in Russian patients
2020 · М.Е. Иванова, А.М. Демчинский, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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DNA methylation markers of breast cancer response to anthracycline based neoadjuvant chemotherapy
2019 · V.O. Sigin, V.V. Strelnikov, et al. · Annals of Oncology
Genetic screening of Russian Usher syndrome patients toward selection for gene therapy
2019 · Ivanova, Marianna E., Trubilin, Vladimir N., et al. · Figshare
PBRM1 is a novel candidate low-penetrance familial cancer predisposition gene
2018 · I. Volodin, V.M. Kozlova, et al. · Annals of Oncology
Результаты использования новой медицинской технологии комплексной ДНК-диагностики синдрома Сотоса
2018 · Ilya V. Volodin, А. С. Танас, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
Works count: 19
Citation count: 147
H-index: 5
I10-index: 4
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