| Pan-cancer analysis of whole genomes TITPCAWG Consortium Nature 578 (7793), 82, 2020 | 1688* | 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 | 547* | 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 | 159 | 2020 |
| Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma H Suzuki, SA Kumar, S Shuai, A Diaz-Navarro, A Gutierrez-Fernandez, ... Nature 574 (7780), 707-711, 2019 | 147 | 2019 |
| The U1 spliceosomal RNA is recurrently mutated in multiple cancers S Shuai, H Suzuki, A Diaz-Navarro, F Nadeu, SA Kumar, ... Nature 574 (7780), 712-716, 2019 | 144 | 2019 |
| 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 | 136 | 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 | 93 | 2020 |
| Candidate cancer driver mutations in distal regulatory elements and long-range chromatin interaction networks H Zhu, L Uusküla-Reimand, K Isaev, L Wadi, A Alizada, S Shuai, V Huang, ... Molecular cell 77 (6), 1307-1321. e10, 2020 | 72* | 2020 |
| Recurrent noncoding regulatory mutations in pancreatic ductal adenocarcinoma ME Feigin, T Garvin, P Bailey, N Waddell, DK Chang, DR Kelley, S Shuai, ... Nature genetics 49 (6), 825-833, 2017 | 68 | 2017 |
| Combined burden and functional impact tests for cancer driver discovery using DriverPower S Shuai, S Gallinger, LD Stein Nature communications 11 (1), 734, 2020 | 41 | 2020 |
| PCAWG Drivers and Functional Interpretation Working Group, Gallinger S, Stein L, PCAWG Consortium S Shuai Combined burden and functional impact tests for cancer driver discovery …, 2020 | 9 | 2020 |
| Cdx1b protects intestinal cell fate by repressing signaling networks for liver specification Q Jin, Y Gao, S Shuai, Y Chen, K Wang, J Chen, J Peng, C Gao Journal of Genetics and Genomics 49 (12), 1101-1113, 2022 | 6 | 2022 |
| PanCancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2 P Bousquets-Muñoz, A Díaz-Navarro, F Nadeu, A Sánchez-Pitiot, ... NPJ Genomic Medicine 7 (1), 19, 2022 | 3 | 2022 |
| Author Correction: Pan-cancer analysis of whole genomes Nature 614 (7948), E39-E39, 2023 | 1 | 2023 |
| Author Correction: 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 614 (7948), E40-E40, 2023 | 1 | 2023 |
| Interruption of Klf5 acetylation in basal progenitor cells promotes luminal commitment by activating Notch signaling B Zhang, S Xia, M Liu, X Li, S Shuai, W Tao, Y Li, JJ Ni, W Zhou, L Liao, ... Journal of genetics and genomics, S1673-8527 (21) 00367-2, 2021 | 1 | 2021 |
| In CLL the U1 snRNA driver mutation alters splicing in multiple genes and pathways A Senff-Ribeiro, F Almodaresi, Q Trinh, S Shuai, D Spaner, XS Puente, ... Cancer Research 83 (7_Supplement), 3814-3814, 2023 | | 2023 |
| 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 614 (7948), E40-E40, 2023 | | 2023 |
| Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (vol 578, pg 102, 2020) E Rheinbay, MM Nielsen, F Abascal, JA Wala, O Shapira, G Tiao, ... NATURE, 2023 | | 2023 |
| Cell type-specific consequences of mosaic structural variants in hematopoietic stem and progenitor cells K Grimes, H Jeong, A Amoah, N Xu, J Niemann, B Raeder, P Hasenfeld, ... bioRxiv, 2023.07. 25.550502, 2023 | | 2023 |
Lincoln SteinDirector of Informatics and Biocomputing, Ontario Institute for Cancer Research Verified email at oicr.on.ca
