| Rare variant contribution to human disease in 281,104 UK Biobank exomes Q Wang, RS Dhindsa, K Carss, AR Harper, A Nag, I Tachmazidou, ... Nature 597 (7877), 527-532, 2021 | 352 | 2021 |
| mRNA 3'uridylation and poly (A) tail length sculpt the mammalian maternal transcriptome. M Morgan, C Much, M DiGiacomo, C Azzi, I Ivanova, DM Vitsios, J Pistolic, ... Nature 548 (7667), 347-351, 2017 | 180 | 2017 |
| Chimira: analysis of small RNA sequencing data and microRNA modifications DM Vitsios, AJ Enright Bioinformatics 31 (20), 3365-3367, 2015 | 114 | 2015 |
| Genetic regulation of the human plasma proteome in 54,306 UK Biobank participants BB Sun, J Chiou, M Traylor, C Benner, YH Hsu, TG Richardson, ... BioRxiv, 2022.06. 17.496443, 2022 | 105 | 2022 |
| Rare variant associations with plasma protein levels in the UK Biobank RS Dhindsa, OS Burren, BB Sun, BP Prins, D Matelska, E Wheeler, ... Nature 622 (7982), 339-347, 2023 | 74 | 2023 |
| Mirnovo: genome-free prediction of microRNAs from small RNA sequencing data and single-cells using decision forests DM Vitsios, E Kentepozidou, L Quintais, E Benito-Gutiérrez, ... Nucleic acids research 45 (21), e177-e177, 2017 | 68 | 2017 |
| Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning D Vitsios, RS Dhindsa, L Middleton, AB Gussow, S Petrovski Nature communications 12 (1), 1504, 2021 | 65 | 2021 |
| A programmed wave of uridylation-primed mRNA degradation is essential for meiotic progression and mammalian spermatogenesis M Morgan, Y Kabayama, C Much, I Ivanova, M Di Giacomo, ... Cell research 29 (3), 221-232, 2019 | 65 | 2019 |
| Spontaneous coronary artery dissection: insights on rare genetic variation from genome sequencing KJ Carss, AA Baranowska, J Armisen, TR Webb, SE Hamby, ... Circulation: Genomic and Precision Medicine 13 (6), e003030, 2020 | 63 | 2020 |
| Large-scale analysis of microRNA expression, epi-transcriptomic features and biogenesis DM Vitsios, MP Davis, S van Dongen, AJ Enright Nucleic acids research 45 (3), 1079-1090, 2017 | 61 | 2017 |
| Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis RS Dhindsa, J Mattsson, A Nag, Q Wang, LV Wain, R Allen, EM Wigmore, ... Communications biology 4 (1), 392, 2021 | 56 | 2021 |
| Exome-based rare-variant analyses in CKD S Cameron-Christie, CJ Wolock, E Groopman, S Petrovski, ... Journal of the American Society of Nephrology 30 (6), 1109-1122, 2019 | 53 | 2019 |
| Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A CA Steward, J Roovers, MM Suner, JM Gonzalez, ... npj Genomic Medicine 4 (1), 31, 2019 | 36 | 2019 |
| Mantis-ml: disease-agnostic gene prioritization from high-throughput genomic screens by stochastic semi-supervised learning D Vitsios, S Petrovski The American Journal of Human Genetics 106 (5), 659-678, 2020 | 31 | 2020 |
| A minimal role for synonymous variation in human disease RS Dhindsa, Q Wang, D Vitsios, OS Burren, F Hu, JE DiCarlo, L Kruglyak, ... The American Journal of Human Genetics 109 (12), 2105-2109, 2022 | 29 | 2022 |
| DrugnomeAI is an ensemble machine-learning framework for predicting druggability of candidate drug targets A Raies, E Tulodziecka, J Stainer, L Middleton, RS Dhindsa, P Hill, ... Communications Biology 5 (1), 1291, 2022 | 27 | 2022 |
| Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes A Nag, RS Dhindsa, J Mitchell, C Vasavda, AR Harper, D Vitsios, ... Science advances 8 (46), eadd5430, 2022 | 26 | 2022 |
| A MILI-independent piRNA biogenesis pathway empowers partial germline reprogramming L Vasiliauskaitė, D Vitsios, RV Berrens, C Carrieri, W Reik, AJ Enright, ... Nature structural & molecular biology 24 (7), 604-606, 2017 | 20 | 2017 |
| Real-time urban traffic information extraction from GPS tracking of a bus fleet E Denaxas, S Mpollas, D Vitsios, C Zolotas, DG Bleris, GM Spanos, ... 2013 IEEE Symposium on Computational Intelligence in Vehicles and …, 2013 | 17 | 2013 |
| Disease prediction with multi-omics and biomarkers empowers case–control genetic discoveries in the UK Biobank M Garg, M Karpinski, D Matelska, L Middleton, OS Burren, F Hu, ... Nature Genetics 56 (9), 1821-1831, 2024 | 14 | 2024 |
Slavé PetrovskiAstraZeneca Centre for Genomics ResearchEmail verificata su unimelb.edu.au