Warren Emmett
Warren Emmett
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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
Recursive splicing in long vertebrate genes
CR Sibley, W Emmett, L Blazquez, A Faro, N Haberman, M Briese, ...
Nature 521 (7552), 371-375, 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
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
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
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
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
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
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
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
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
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
ParkDB: a Parkinson’s disease gene expression database
C Taccioli, V Maselli, J Tegner, D Gomez-Cabrero, G Altobelli, W Emmett, ...
Database 2011, 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
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
UCbase 2.0: ultraconserved sequences database (2014 update)
V Lomonaco, R Martoglia, F Mandreoli, L Anderlucci, W Emmett, ...
Database 2014, 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
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
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
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
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