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 | 202 | 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 | 161 | 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 | 159 | 2018 |
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 | 135 | 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 | 133 | 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, 1-17, 2017 | 101 | 2017 |
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), 10.1128/mbio. 00840-13, 2013 | 95 | 2013 |
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 | 82 | 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 | 62 | 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 | 59 | 2013 |
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 | 56 | 2019 |
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 | 56 | 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 | 50 | 2013 |
ParkDB: a Parkinson’s disease gene expression database C Taccioli, V Maselli, J Tegnér, D Gomez-Cabrero, G Altobelli, W Emmett, ... Database 2011, bar007, 2011 | 43 | 2011 |
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 | 41 | 2021 |
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 | 36 | 2014 |
UCbase 2.0: ultraconserved sequences database (2014 update) V Lomonaco, R Martoglia, F Mandreoli, L Anderlucci, W Emmett, ... Database 2014, bau062, 2014 | 28 | 2014 |
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 | 27 | 2016 |
Molecular residual disease detection in early stage breast cancer with a personalized sequencing approach RJ Cutts, M Coakley, I Garcia-Murillas, L Ulrich, K Howarth, W Emmett, ... Cancer Research 81 (13_Supplement), 536-536, 2021 | 8 | 2021 |
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 |