| Multi-omics-based identification of SARS-CoV-2 infection biology and candidate drugs against COVID-19 D Barh, S Tiwari, ME Weener, V Azevedo, A Góes-Neto, MM Gromiha, ... Computers in biology and medicine 126, 104051, 2020 | 104 | 2020 |
| Combinatorial approaches for cancer treatment using oncolytic viruses: projecting the perspectives through clinical trials outcomes A Malogolovkin, N Gasanov, A Egorov, M Weener, R Ivanov, ... Viruses 13 (7), 1271, 2021 | 49 | 2021 |
| Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease− associated genes SE de Bruijn, K Rodenburg, J Corominas, T Ben-Yosef, J Reurink, ... Genetics in Medicine 25 (3), 100345, 2023 | 32 | 2023 |
| The spike of SARS-CoV-2: uniqueness and applications R Kumavath, D Barh, BS Andrade, M Imchen, FF Aburjaile, A Ch, ... Frontiers in Immunology 12, 663912, 2021 | 32 | 2021 |
| A novel multi-omics-based highly accurate prediction of symptoms, comorbid conditions, and possible long-term complications of COVID-19 D Barh, S Tiwari, BS Andrade, ME Weener, A Goes-Neto, V Azevedo, ... Molecular omics 17 (2), 317-337, 2021 | 28 | 2021 |
| Stargardt disease-associated mutation spectrum of a Russian Federation cohort IV Zolnikova, VV Strelnikov, NA Skvortsova, AS Tanas, D Barh, ... European Journal of Medical Genetics 60 (2), 140-147, 2017 | 26 | 2017 |
| Genetic screening of Russian Usher syndrome patients toward selection for gene therapy ME Ivanova, VN Trubilin, DS Atarshchikov, AM Demchinsky, VV Strelnikov, ... Ophthalmic Genetics 39 (6), 706-713, 2018 | 21 | 2018 |
| Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction J Reurink, N Weisschuh, A Garanto, A Dockery, LI van den Born, I Fajardy, ... Human Genetics and Genomics Advances 4 (2), 2023 | 19 | 2023 |
| Potential molecular mechanisms of rare anti-tumor immune response by SARS-CoV-2 in isolated cases of lymphomas D Barh, S Tiwari, L Gabriel Rodrigues Gomes, ME Weener, KJ Alzahrani, ... Viruses 13 (10), 1927, 2021 | 16 | 2021 |
| Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype N Jurkute, F Cancellieri, L Pohl, CHZ Li, RA Heaton, J Reurink, ... NPJ Genomic Medicine 7 (1), 60, 2022 | 15 | 2022 |
| Novel frameshift mutation in NYX gene in a Russian family with complete congenital stationary night blindness ME Ivanova, IV Zolnikova, KV Gorgisheli, DS Atarshchikov, P Ghosh, ... Ophthalmic genetics 40 (6), 558-563, 2019 | 8 | 2019 |
| Подходы к молекулярно-генетической диагностике глазных проявлений пролиферативного синдрома для патофизиологически направленного лечения МЕ Винер, НА Бакунина, ЖМ Салмаси, ГВ Порядин, Б Дебмала, ... РМЖ. Клиническая офтальмология 22 (1), 16-22, 2022 | 6 | 2022 |
| Evaluation of cortical visual prostheses microelectrode array function. Description of behavioral feline model ME Ivanova, SA Gordeev, VV Ortmann, BK Baziyan 2008 30th Annual International Conference of the IEEE Engineering in …, 2008 | 5 | 2008 |
| Pathophysiological features of the visual cycle, cascade and metabolic pathways in retinitis pigmentosa ME Weener, DS Atarshchikov, VV Kadyshev, IV Zolnikova, ... Russian Ophthalmological Journal 14 (1), 80-88, 2021 | 3 | 2021 |
| Early audiological phenotype in patients with mutations in the USH2A gene TG Markova, MR Lalayants, NN Alekseeva, OP Ryzhkova, OL Shatokhina, ... International Journal of Pediatric Otorhinolaryngology 157, 111140, 2022 | 2 | 2022 |
| Особенности патофизиологии зрительного цикла, каскада и метаболических путей при пигментном ретините МЕ Винер, ДС Атарщиков, ВВ Кадышев, ИВ Зольникова, ... Российский офтальмологический журнал 14 (1), 80-88, 2021 | 2 | 2021 |
| A novel multi-omics-based identification of symptoms, comorbid conditions, and possible long-term complications in COVID-19 D Barh, S Tiwari, BS Andrade, ME Weener, A Góes-Neto, V Azevedo, ... medRxiv, 2020.12. 08.20245753, 2020 | 2 | 2020 |
| Whole exome sequencing reveals novel EYS mutations in Russian patients with autosomal recessive retinitis pigmentosa MY Ivanova, D Atarshchikov, E Pomerantseva, E Tolmacheva, ... Investigative Ophthalmology & Visual Science 61 (7), 675-675, 2020 | 2 | 2020 |
| Are We Ready for Real-Time Applications of Clinical NGS D Barh, ME Ivanova, V Azevedo Next Generat Sequenc & Applic 2, 122, 2015 | 1 | 2015 |
| Combination of digital and experimental tools to enhance bulk deep intronic variants pathogenicity prediction to better diagnose inherited retinal disorders (IRDs) M Weener, E Place, J Straubhaar, H Scott, S Mehrotra, KM Bujakowska, ... Investigative Ophthalmology & Visual Science 65 (7), 4940-4940, 2024 | | 2024 |
Debmalya Barh; Ph.D.Institute of Integrative Omics and Applied Biotechnology (IIOAB), WB, India & UFMG, Brazil確認したメール アドレス: ufmg.br