| Molecular relationships between bronchial asthma and hypertension as comorbid diseases EY Bragina, IA Goncharova, AF Garaeva, EV Nemerov, AA Babovskaya, ... Journal of integrative bioinformatics 15 (4), 20180052, 2018 | 22 | 2018 |
| Analysis of cytokine networks genes in the development of «inverse» comorbidity between asthma and tuberculosis EY Bragina, MB Freidin, NP Babushkina, AF Garaeva, OV Kolokolova, ... Medical Genetics 16 (1), 20-24, 2017 | 10 | 2017 |
| Putative regulatory functions of SNPs associated with bronchial asthma, arterial hypertension and their comorbid phenotype IA Goncharova, EY Bragina, IZ Zhalsanova, MB Freidin, MS Nazarenko Vavilov Journal of Genetics and Breeding 25 (8), 855, 2021 | 7 | 2021 |
| Analysis of haplotypes of CAT, TLR4, and IL10 genes in bronchial asthma patients comorbid with arterial hypertension EY Bragina, IA Goncharova, MB Freidin, IZ Zhalsanova, DE Gomboeva, ... Сибирский научный медицинский журнал 39 (6), 55-64, 2020 | 6* | 2020 |
| Genetic comorbidity of hypertension and bronchial asthma EY Bragina, IA Goncharova, IZ Zhalsanova, EV Nemerov, MS Nazarenko, ... Arterial’naya Gipertenziya (Arterial Hypertension), 2022 | 2 | 2022 |
| Modifier genes as a cause of Wilson–Konovalov disease clinical polymorphism AE Postrigan, IZ Zhalsanova, EA Fonova, NA Skryabin Russian Journal of Genetics 57, 522-532, 2021 | 2 | 2021 |
| Clinical and pathophysiological aspects of non-motor manifestations of Parkinson's disease MA Nikitina, NG Zhukova, EY Bragina, VM Alifirova, IA Zhukova, ... Bulletin of Siberian Medicine 18 (4), 222-232, 2020 | 2 | 2020 |
| The role of the TNF (rs1800629), TNFB (rs2239704) and TNFRSF1B (rs652625) genes polymorphic variants in the allergic and infectious disease's development IZ Zhalsanova, EY Bragina, NP Babushkina, NV Tarasenko, ... Medical Genetics 19 (8), 90-91, 2020 | 2 | 2020 |
| The ATOX1 Gene Role in Copper Metabolism and the Pathogenesis of Copper-Induced Diseases IZ Zhalsanova, EA Fonova, DI Zhigalina, NA Skryabin Russian Journal of Genetics 59 (3), 242-250, 2023 | 1 | 2023 |
| Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing. AA Sivtsev, IZ Zhalsanova, AE Postrigan, EA Fonova, OY Vasilyeva, ... Klinicheskaia Laboratornaia Diagnostika 67 (4), 250-256, 2022 | 1 | 2022 |
| Analysis of mutation spectrum of COL1A1 and COL1A2 genes using massively parallel sequencing in patients with osteogenesis imperfecta in the Tomsk region NA Skryabin, OY Vasilyeva, AA Sivtsev, IZ Zhalsanova, AE Postrigan, ... Medical Genetics 19 (1), 38-45, 2020 | 1 | 2020 |
| Generation of an Induced Pluripotent Stem Cell Line TNRMCi001-A by Reprogramming Fibroblasts from a Homozygous F508del Cystic Fibrosis Patient DI Zhigalina, TN Kireeva, TV Nikitina, ON Odinokova, NA Kolesnikov, ... Russian Journal of Developmental Biology 54 (Suppl 1), S68-S74, 2023 | | 2023 |
| Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI IZ Zhalsanova, AE Postrigan, NR Valiakhmetov, NA Kolesnikov, ... International Journal of Molecular Sciences 24 (7), 6672, 2023 | | 2023 |
| The ATOX1 Gene Role in Copper Metabolism and in the Copper-Induced Diseases Pathogenesis IZ Zhalsanova, EA Fonova, DI Zhigalina, NA Skryabin Genetika 59 (3), 283-293, 2023 | | 2023 |
| Case Report: Compound Heterozygous Variants of the MAN1B1 Gene in a Russian Patient with Rafiq Syndrome IZ Zhalsanova, EG Ravzhaeva, AE Postrigan, GN Seitova, DI Zhigalina, ... International Journal of Molecular Sciences 23 (18), 10606, 2022 | | 2022 |
| RMetSeq package for processing targeted MRE-seq A Zarubin, A Sivtsev, I Zhalsanova, N Skryabin Bioinformatics of Genome Regulation and Structure/Systems Biology (BGRS/SB …, 2022 | | 2022 |
| Understanding the role of genetics in comorbidity EY Bragina, IA Goncharova, IZ Zhalsanova, EV Nemerov, MS Nazarenko, ... Bioinformatics of Genome Regulation and Structure/Systems Biology (BGRS/SB …, 2022 | | 2022 |
| Functional consequences of rs1800629 TNF gene associated with asthma and tuberculosis development I Zhalsanova, E Bragina, N Babushkina, N Tarasenko, M Freidin, ... | | 2022 |
| 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 … DI Zhigalina, AA Malakhova, OY Vasilyeva, EV Grigor'eva, AA Sivtsev, ... Stem Cell Research 57, 102556, 2021 | | 2021 |
| Genetic and clinical characteristic of Wilson-Konovalov disease in the Siberian region IZ Zhalsanova, EA Fonova, AA Sivcev, AE Postrigan, TA Sakovskaya, ... Medical Genetics 20 (10), 53-56, 2021 | | 2021 |
