| Congenital myasthenic syndrome type 19 is caused by mutations in COL13A1, encoding the atypical non-fibrillar collagen type XIII α1 chain CV Logan, J Cossins, PMR Cruz, DA Parry, S Maxwell, ... The American Journal of Human Genetics 97 (6), 878-885, 2015 | 72 | 2015 |
| Primary cilia, ciliogenesis and the actin cytoskeleton: a little less resorption, a little more actin please CEL Smith, AVR Lake, CA Johnson Frontiers in cell and developmental biology 8, 622822, 2020 | 71 | 2020 |
| Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin Please. Front Cell Dev Biol. 2020; 8: 622822 CEL Smith, AVR Lake, CA Johnson | 5 | 2020 |
| Racgap1 knockdown results in cells with multiple cilia due to cytokinesis failure B Basu, AVR Lake, B China, K Szymanska, G Wheway, S Bell, E Morrison, ... Annals of Human Genetics 88 (1), 45-57, 2024 | 1 | 2024 |
| Drug and siRNA screens identify ROCK2 as a therapeutic target for ciliopathies AVR Lake, CEL Smith, S Natarajan, B Basu, SK Best, T Stevenson, ... bioRxiv, 2020.11. 26.393801, 2020 | 1 | 2020 |
| Reverse genetics siRNA-based visual phenotype screen datasets identifying genes involved in supernumerary primary cilium formation B Basu, A Lake, K Szymanska, G Wheway, S Bell, E Morrison, J Bond, ... University of Leeds, 2021 | | 2021 |
| Identifying novel regulators of ciliogenesis AVR Lake University of Leeds, 2020 | | 2020 |
