| Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome AC Thomas, H Williams, N Setó-Salvia, C Bacchelli, D Jenkins, ... The American Journal of Human Genetics 95 (5), 611-621, 2014 | 105 | 2014 |
| The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes AM Waters, R Asfahani, P Carroll, L Bicknell, F Lescai, A Bright, ... Journal of medical genetics, jmedgenet-2014-102691, 2015 | 93 | 2015 |
| Towards the prevention of aminoglycoside-related hearing loss ME O'Sullivan, A Perez, R Lin, A Sajjadi, AJ Ricci, AG Cheng Frontiers in Cellular Neuroscience 11, 325, 2017 | 88 | 2017 |
| Mechanotransduction-dependent control of stereocilia dimensions and row identity in inner hair cells JF Krey, P Chatterjee, RA Dumont, M O’Sullivan, D Choi, JE Bird, ... Current Biology, 2020 | 56 | 2020 |
| Mitochondrial m. 1584A 12S m62A rRNA methylation in families with m. 1555A> G associated hearing loss M O'Sullivan, P Rutland, D Lucas, E Ashton, S Hendricks, S Rahman, ... Human molecular genetics 24 (4), 1036-1044, 2015 | 40 | 2015 |
| Dissociating antibacterial from ototoxic effects of gentamicin C-subtypes ME O’Sullivan, Y Song, R Greenhouse, R Lin, A Perez, PJ Atkinson, ... Proceedings of the National Academy of Sciences, 2020 | 36 | 2020 |
| Aminoglycoside ribosome interactions reveal novel conformational states at ambient temperature ME O’Sullivan, F Poitevin, RG Sierra, C Gati, EH Dao, Y Rao, F Aksit, ... Nucleic acids research 46 (18), 9793-9804, 2018 | 23 | 2018 |
| Mind Your Ears: A New Antidote to Aminoglycoside Toxicity? ME O’Sullivan, AG Cheng Journal of medicinal chemistry, 2017 | 7 | 2017 |
