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| The evolutionary history of 2,658 cancers M Gerstung, C Jolly, I Leshchiner, SC Dentro, S Gonzalez, D Rosebrock, ... Nature 578 (7793), 122-128, 2020 | 1013 | 2020 |
| Patterns of somatic structural variation in human cancer genomes Y Li, ND Roberts, JA Wala, O Shapira, SE Schumacher, K Kumar, ... Nature 578 (7793), 112-121, 2020 | 825 | 2020 |
| Analyses of non-coding somatic drivers in 2,658 cancer whole genomes E Rheinbay, MM Nielsen, F Abascal, JA Wala, O Shapira, G Tiao, ... Nature 578 (7793), 102-111, 2020 | 584 | 2020 |
| Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis J Carlevaro-Fita, A Lanzós, L Feuerbach, C Hong, D Mas-Ponte, ... Communications biology 3 (1), 56, 2020 | 187 | 2020 |
| A systematic review of artificial intelligence techniques in cancer prediction and diagnosis Y Kumar, S Gupta, R Singla, YC Hu Archives of Computational Methods in Engineering 29 (4), 2043-2070, 2022 | 185 | 2022 |
| Integrative pathway enrichment analysis of multivariate omics data M Paczkowska, J Barenboim, N Sintupisut, NS Fox, H Zhu, D Abd-Rabbo, ... Nature communications 11 (1), 735, 2020 | 180 | 2020 |
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| De novo sequence and copy number variants are strongly associated with Tourette disorder and implicate cell polarity in pathogenesis S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ... Cell reports 24 (13), 3441-3454. e12, 2018 | 133 | 2018 |
| Divergent mutational processes distinguish hypoxic and normoxic tumours V Bhandari, CH Li, RG Bristow, PC Boutros Nature communications 11 (1), 737, 2020 | 121 | 2020 |
| Pathway and network analysis of more than 2500 whole cancer genomes MA Reyna, D Haan, M Paczkowska, LPC Verbeke, M Vazquez, ... Nature communications 11 (1), 729, 2020 | 114 | 2020 |
| High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations Y Zhang, F Chen, NA Fonseca, Y He, M Fujita, H Nakagawa, Z Zhang, ... Nature communications 11 (1), 736, 2020 | 73 | 2020 |
| Inferring structural variant cancer cell fraction M Cmero, K Yuan, CS Ong, J Schröder, NM Corcoran, T Papenfuss, ... Nature communications 11 (1), 730, 2020 | 47 | 2020 |
| Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig Y Rubanova, R Shi, CF Harrigan, R Li, J Wintersinger, N Sahin, ... Nature communications 11 (1), 731, 2020 | 47 | 2020 |
| Combined burden and functional impact tests for cancer driver discovery using DriverPower S Shuai, S Gallinger, LD Stein Nature communications 11 (1), 734, 2020 | 43 | 2020 |
| Massive interstitial copy-neutral loss-of-heterozygosity as evidence for cancer being a disease of the DNA-damage response Y Kumar, J Yang, T Hu, L Chen, Z Xu, L Xu, XX Hu, G Tang, JM Wang, ... BMC medical genomics 8, 1-21, 2015 | 24 | 2015 |
| Forward and reverse mutations in stages of cancer development T Hu, Y Kumar, I Shazia, SJ Duan, Y Li, L Chen, JF Chen, R Yin, A Kwong, ... Human genomics 12, 1-21, 2018 | 18 | 2018 |
| Copy number variation analysis based on AluScan sequences JF Yang, XF Ding, L Chen, WK Mat, MZ Xu, JF Chen, JM Wang, L Xu, ... Journal of Clinical Bioinformatics 4, 1-14, 2014 | 17 | 2014 |
| Rustam; Shukla, J.; Mukhopadhyay, P., Halogenbonded assemblies of arylene imides and diimides: insight from electronic, structural, and computational studies K Mandal, D Bansal, Y Kumar Chem. Eur. J 26 (46), 10607-10619, 2020 | 13 | 2020 |