| Astrovirus VA1/HMO-C: an increasingly recognized neurotropic pathogen in immunocompromised patients JR Brown, S Morfopoulou, J Hubb, WA Emmett, W Ip, D Shah, T Brooks, ... Clinical Infectious Diseases 60 (6), 881-888, 2015 | 176 | 2015 |
| Recursive splicing in long vertebrate genes CR Sibley, W Emmett, L Blazquez, A Faro, N Haberman, M Briese, ... Nature 521 (7552), 371-375, 2015 | 139 | 2015 |
| Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis P Fratta, P Sivakumar, J Humphrey, K Lo, T Ricketts, H Oliveira, ... The EMBO journal 37 (11), e98684, 2018 | 119 | 2018 |
| Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy M Schmidts, J Vodopiutz, S Christou-Savina, CR Cortés, ... The American Journal of Human Genetics 93 (5), 932-944, 2013 | 119 | 2013 |
| Heteromeric RNP assembly at LINEs controls lineage-specific RNA processing J Attig, F Agostini, C Gooding, AM Chakrabarti, A Singh, N Haberman, ... Cell 174 (5), 1067-1081. e17, 2018 | 97 | 2018 |
| Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains S Goh, H Hussain, BJ Chang, W Emmett, TV Riley, P Mullany MBio 4 (6), e00840-13, 2013 | 83 | 2013 |
| Quantitative analysis of cryptic splicing associated with TDP-43 depletion J Humphrey, W Emmett, P Fratta, AM Isaacs, V Plagnol BMC medical genomics 10 (1), 1-17, 2017 | 68 | 2017 |
| Exon junction complex shapes the transcriptome by repressing recursive splicing L Blazquez, W Emmett, R Faraway, JMB Pineda, S Bajew, A Gohr, ... Molecular cell 72 (3), 496-509. e9, 2018 | 67 | 2018 |
| Splicing repression allows the gradual emergence of new Alu-exons in primate evolution J Attig, I Ruiz de los Mozos, N Haberman, Z Wang, W Emmett, K Zarnack, ... elife 5, e19545, 2016 | 50 | 2016 |
| Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans V Berry, C Gregory-Evans, W Emmett, N Waseem, J Raby, DQ Prescott, ... European Journal of Human Genetics 21 (12), 1356-1360, 2013 | 50 | 2013 |
| Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated LRRK2 Locus D Trabzuni, M Ryten, W Emmett, A Ramasamy, KJ Lackner, T Zeller, ... PloS one 8 (8), e70724, 2013 | 50 | 2013 |
| DNA methylation analysis of murine hematopoietic side population cells during aging O Taiwo, GA Wilson, W Emmett, T Morris, D Bonnet, E Schuster, ... Epigenetics 8 (10), 1114-1122, 2013 | 43 | 2013 |
| ParkDB: a Parkinson’s disease gene expression database C Taccioli, V Maselli, J Tegner, D Gomez-Cabrero, G Altobelli, W Emmett, ... Database 2011, 2011 | 39 | 2011 |
| FICC-Seq: a method for enzyme-specified profiling of methyl-5-uridine in cellular RNA JM Carter, W Emmett, IR Mozos, A Kotter, M Helm, J Ule, S Hussain Nucleic acids research 47 (19), e113-e113, 2019 | 37 | 2019 |
| The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance I Conte, S Merella, JM Garcia-Manteiga, C Migliore, D Lazarevic, ... Nucleic acids research 42 (12), 7793-7806, 2014 | 32 | 2014 |
| UCbase 2.0: ultraconserved sequences database (2014 update) V Lomonaco, R Martoglia, F Mandreoli, L Anderlucci, W Emmett, ... Database 2014, 2014 | 28 | 2014 |
| MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration R Simone, F Javad, W Emmett, OG Wilkins, FL Almeida, ... Nature 594 (7861), 117-123, 2021 | 26 | 2021 |
| Variants Within TSC2 Exons 25 and 31 Are Very Unlikely to Cause Clinically Diagnosable Tuberous Sclerosis R Ekong, M Nellist, M Hoogeveen‐Westerveld, M Wentink, J Panzer, ... Human mutation 37 (4), 364-370, 2016 | 20 | 2016 |
| International Parkinson Disease Genomics C D Trabzuni, M Ryten, W Emmett, A Ramasamy, KJ Lackner, T Zeller, ... Hernandez D, Nalls MA, Sharma M, Garnier S, Lesage S, Simon-Sanchez J …, 2013 | 7 | 2013 |
| Clark JR Brown, S Morfopoulou, J Hubb, WA Emmett, W Ip, D Shah, T Brooks, ... DA, Plagnol, V., Jacques, TS, Qasim, W., Hubank, M., Breuer, J, 2015 | 5 | 2015 |
