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Degradation of Cellular miR-27 by a Novel, Highly Abundant Viral Transcript Is Important for Efficient Virus Replication In Vivo L Marcinowski, M Tanguy, A Krmpotic, B Rädle, VJ Lisnić, L Tuddenham, ... PLoS pathogens 8 (2), e1002510, 2012 | 214 | 2012 |
Cytomegalovirus microRNAs facilitate persistent virus infection in salivary glands L Dölken, A Krmpotic, S Kothe, L Tuddenham, M Tanguy, L Marcinowski, ... PLoS pathogens 6 (10), e1001150, 2010 | 75 | 2010 |
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes W Wei, KR Schon, G Elgar, A Orioli, M Tanguy, A Giess, M Tischkowitz, ... Nature 611 (7934), 105-114, 2022 | 72 | 2022 |
Antiviral RNA interference against Orsay virus is neither systemic nor transgenerational in Caenorhabditis elegans A Ashe, P Sarkies, J Le Pen, M Tanguy, EA Miska Journal of Virology 89 (23), 12035-12046, 2015 | 56 | 2015 |
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An Alternative STAT Signaling Pathway Acts in Viral Immunity in Caenorhabditis elegans M Tanguy, L Veron, P Stempor, J Ahringer, P Sarkies, E Miska American Society for Microbiology, 2017 | 41 | 2017 |
Deregulation of type I IFN-dependent genes correlates with increased susceptibility to cytomegalovirus acute infection of dicer mutant mice E Ostermann, L Tuddenham, C Macquin, G Alsaleh, J Schreiber-Becker, ... Public Library of Science 7 (8), e43744, 2012 | 40 | 2012 |
Genome sequencing reveals underdiagnosis of primary ciliary dyskinesia in bronchiectasis A Shoemark, H Griffin, G Wheway, C Hogg, JS Lucas, C Camps, J Taylor, ... European Respiratory Journal 60 (5), 2022 | 28 | 2022 |
Antiviral RNA interference in animals: piecing together the evidence M Tanguy, EA Miska Nature Structural & Molecular Biology 20 (11), 1239-1241, 2013 | 21 | 2013 |
SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile R Al-Jawahiri, A Foroutan, J Kerkhof, H McConkey, M Levy, ... Genetics in medicine 24 (6), 1261-1273, 2022 | 20 | 2022 |
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis Z Hyder, E Calpena, Y Pei, RS Tooze, H Brittain, SRF Twigg, D Cilliers, ... Genetics in Medicine 23 (12), 2360-2368, 2021 | 14 | 2021 |
Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’condition H Martins Custodio, LM Clayton, R Bellampalli, S Pagni, K Silvennoinen, ... Brain 146 (9), 3885-3897, 2023 | 11 | 2023 |
Formation of large viroplasms and virulence of Cauliflower mosaic virus in turnip plants depend on the N-terminal EKI sequence of viral protein TAV A Geldreich, G Haas, J Kubina, C Bouton, M Tanguy, M Erhardt, M Keller, ... PLoS One 12 (12), e0189062, 2017 | 11 | 2017 |
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Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration A Vetro, C Pelorosso, S Balestrini, A Masi, S Hambleton, E Argilli, V Conti, ... The American Journal of Human Genetics 110 (8), 1356-1376, 2023 | 10 | 2023 |
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Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease O Sadeghi-Alavijeh, MMY Chan, SH Moochhala, JC Ambrose, ... Kidney International 104 (5), 975-984, 2023 | 7 | 2023 |
Late-onset autosomal dominant macular degeneration caused by deletion of the CRX gene S Yahya, CEL Smith, JA Poulter, M McKibbin, G Arno, J Ellingford, ... Ophthalmology 130 (1), 68-76, 2023 | 7 | 2023 |
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