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| Issue |
Title |
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| Vol 24, No 4 (2025) |
Ethical issues of preconception genetic testing |
Abstract
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E. G. Grebenshchikova |
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| Vol 24, No 3 (2025) |
The role of microRNAs in the pathogenesis and therapy of oncological diseases |
Abstract
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M. A. Omarov, R. M. Gadjiev, A. R. Akhmatnurov, M. H. Musaeva, M. H. Musaeva, M. R. Rasulov, M. R. Rasulov |
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| Vol 24, No 2 (2025) |
Monogenic obesity: modern possibilities of targeted therapy |
Abstract
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D. G. Khubaeva, A. A. Zolina, Z. G. Yurovskih, M. A. Drozhdin, S. R. Khakova, E. A. Kachikeeva, A. R. Khusnullina, I. S. Ermakov, A. A. Kulakov, M. A. Kolesnikov, D. V. Vasileva, D. A. Petrov, A. F. Yusupova |
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| Vol 24, No 2 (2025) |
Violation of DNA methylation as a factor of fetal growth restriction |
Abstract
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M. M. Gavrilenko, E. A. Trifonova, V. A. Stepanov |
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| Vol 24, No 1 (2025) |
Clinical characteristics and modern approaches to diagnostics and therapy of acid sphingomyelinase deficiency (Niemann–Pick disease type AB) |
Abstract
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V. V. Shmarin, A. A. Vasilenko, V. V. Zarubina, T. I. Bocharova, E. Yu. Zakharova |
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| Vol 24, No 1 (2025) |
Brugada syndrome: from genetic diagnostics to personalized therapy |
Abstract
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A. V. Iarmukhametova, A. S. Sergeev, A. P. Filatov, E. R. Shmatkova, K. Iu. Kopytova, A. A. Akhiyarova, A. F. Davletshin, K. A. Salakhova |
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| Vol 23, No 12 (2024) |
PIK3CA-related overgrowth spectrum: molecular mechanism, diagnostic and therapy features |
Abstract
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E. V. Bychkova, N. A. Semenova, G. B. Sagoyan, D. M. Guseva, V. V. Strelnikov |
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| Vol 23, No 11 (2024) |
Spectrum of mutations of the BRCA1, BRCA2, CHEK2 and PALB2 genes in breast cancer |
Abstract
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A. V. Kamysheva, A. V. Kubyshkin, K. A. Aliev, I. I. Fomochkina, D. I. Vodolazhsky |
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| Vol 23, No 9 (2024) |
Review of current research on the development of gene therapy for cystic fibrosis using genome editing techniques |
Abstract
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S. A. Smirnikhina |
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| Vol 23, No 8 (2024) |
Significance of semaphorins in the pathogenesis of obesity development |
Abstract
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A. F. Nikolaeva, N. A. Semenova, T. V. Strokova, M. V. Bulak, V. O. Sigin |
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| Vol 23, No 7 (2024) |
Hereditary prostate cancer |
Abstract
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D. S. Mikhaylenko, D. V. Zaletayev |
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| Vol 23, No 7 (2024) |
Features of clonal evolution in acute myeloid leukemia |
Abstract
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V. V. Musatova, A. V. Efremova |
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| Vol 23, No 6 (2024) |
Single nucleotide polymorphisms in the mark signaling pathway genes (NRAS, KRAS, BRAF) in plasma cell neoplasms |
Abstract
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T. V. Rudenkova, N. N. Klimkovich, S. A. Kostiuk, J. M. Kozich |
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| Vol 23, No 5 (2024) |
Chromosomal instability in gastric cancer |
Abstract
PDF (Rus)
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M. V. Nemtsova, A. D. Molchanov, E. B. Kuznetsova, I. V. Bure |
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| Vol 23, No 4 (2024) |
Disruption of histone lysine methyltransferase genes and specific episignatures |
Abstract
PDF (Rus)
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O. A. Zemlianaia, A. V. Efremova, I. V. Volodin, D. V. Zaletaev |
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| Vol 23, No 3 (2024) |
Balanced X-autosome translocations and male infertility |
Abstract
PDF (Rus)
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M. V. Andreeva, L. F. Kurilo, V. B. Chernykh |
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| Vol 23, No 3 (2024) |
Organisational complexities and ethical aspects of identifying incidental findings in whole-genome non-invasive prenatal testing |
Abstract
PDF (Rus)
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E. E. Baranova, V. L. Izhevskaya, E. E. Efremova |
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| Vol 23, No 2 (2024) |
The role of genomics in predicting neuropsychic disorders |
Abstract
PDF (Rus)
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V. M. Minnigaliev, Z. A. Khamadullina, S. A. Shirinyan, A. A. Bakieva, E. I. Islamova, E. K. Makhortykh, G. A. Gayazova, K. I. Sagyndykova, P. M. Kukasova, Yu. O. Umorina, D. A. Chadaeva, E. V. Tishkina |
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| Vol 23, No 2 (2024) |
Heterotaxy syndrome: genetic factors (review) |
Abstract
PDF (Rus)
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S. N. Fedenev, E. V. Kudryavtseva, V. V. Kovalev, N. V. Mostova, K. V. Styukova |
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| Vol 22, No 12 (2023) |
Genome editing of human embryos: the ethics of utilitarianism |
Abstract
PDF (Rus)
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|
A. O. Borisova |
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| Vol 22, No 12 (2023) |
Clinical significance of PIK3CA mutations in breast cancer subtypes |
Abstract
PDF (Rus)
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E. I. Koroleva, V. D. Nazarov, S. V. Lapin, A. V. Vladykina, S. V. Anisimov, I. Yu. Shchelkanova, V. L. Emanuel |
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| Vol 22, No 12 (2023) |
Modern molecular genetic methods and approaches used in the preconception carrier screening |
Abstract
PDF (Rus)
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Yu. A. Nasykhova, L. A. Karpovich, N. M. Dvoynova, N. S. Osinovskaya, A. S. Glotov |
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| Vol 22, No 12 (2023) |
Multilocus imprinting disturbances |
Abstract
PDF (Rus)
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E. G. Panchenko, O. A. Simonova, V. V. Strelnikov |
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| Vol 22, No 12 (2023) |
Sperm mitochondrial DNA copy number and male fertility |
Abstract
PDF (Rus)
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S. Sh. Khayat, L. F. Kurilo, V. B. Chernykh |
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| Vol 22, No 11 (2023) |
Ethical aspects of whole-genome noninvasive prenatal testing |
Abstract
PDF (Rus)
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A. A. Potapov, M. T. Kaplanova, A. M. Galaktionova, E. E. Baranova, O. V. Sagaydak, V. L. Izhevskaya, A. G. Denisov |
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| Vol 22, No 9 (2023) |
Prevalence of the filaggrin gene loss-of-function variants in different countries and the effect of their carriage on the course of atopic dermatitis |
Abstract
PDF (Rus)
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| Vol 22, No 5 (2023) |
The first results and prospects of medical genetic studies of museum and archaeological samples |
Abstract
PDF (Rus)
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T. V. Andreeva, A. S. Bydanov, F. E. Gusev, E. I. Rogaev |
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| Vol 22, No 5 (2023) |
Digitalization of Russian Biobanks for Medical Genetic Studies: Problems and Prospects |
Abstract
PDF (Rus)
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A. S. Glotov, O. Yu. Yartseva, Yu. A. Nasykhova, T. E. Lazareva, Yu. A. Barbitov, A. D. Martynov, T. M. Akhmerov |
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| Vol 22, No 3 (2023) |
Role of LncRNA H19 in developing obesity, and potential regulatory mechanism of its differential expression |
Abstract
PDF (Rus)
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M. N. Ammar, N. P. Milutina, E. V. Butenko, R. M. Ali, T. P. Shkurat |
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| Vol 21, No 4 (2022) |
Leigh syndrome: clinical and molecular genetic features, modern approaches to diagnosis and therapy |
Abstract
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D. V. Kistol, P. G. Tsygankova, E. Yu. Zakharova |
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| Vol 21, No 4 (2022) |
Informed consent for genetic testing and screening |
Abstract
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V. L. Izhevskaya, E. E. Baranova |
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| Vol 21, No 5 (2022) |
Е-cadherin in gastric cancer tumorigenesis |
Abstract
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M. V. Nemtsova, I. V. Bure, D. V. Zaletaev, E. B. Kuznetsova, E. A. Vetchinkina, A. D. Molchanov |
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| Vol 21, No 5 (2022) |
Treatment of tyrosinemia type 1: practical aspects |
Abstract
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E. Yu. Zakharova, V. V. Zarubina, N. A. Krasnoshchekova, N. L. Pechatnikova, V. S. Kakaulina, T. N. Kekeeva, T. V. Bushueva |
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| Vol 21, No 6 (2022) |
Clinical characteristics and epidemiology of lysosomal storage diseases |
Abstract
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V. N. Gorbunova, N. V. Buchinskaia, E. Y. Zakharova |
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| Vol 21, No 6 (2022) |
Lysosomal diseases and common neurodegenerative diseases: a common mechanism of pathogenesis |
Abstract
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D. V. Kistol, E. Y. Zakharova, P. G. Tsygankova |
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