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| Lewis MA, Lachgar-Ruiz M, Di Domenico F, et al. (2024) Pathological mechanisms and candidate therapeutic approaches in the hearing loss of mice carrying human MIR96 mutations. Genome Medicine. 16: 121 |
| Lachgar-Ruiz M, Ingham NJ, Martelletti E, et al. (2024) Two new mouse alleles of Ocm and Slc26a5. Hearing Research. 452: 109109 |
| Chen J, Lewis MA, Wai A, et al. (2024) A new mutation of Sgms1 causes gradual hearing loss associated with a reduced endocochlear potential. Hearing Research. 451: 109091 |
| Zhu W, Du W, Rameshbabu AP, et al. (2024) Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation. Science Translational Medicine. 16: eadn0689 |
| Lewis MA, Schulte J, Matthews L, et al. (2023) Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. Plos Genetics. 19: e1011058 |
| Zhu W, Du W, Rameshbabu AP, et al. (2023) Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation. Biorxiv : the Preprint Server For Biology |
| Martelletti E, Ingham NJ, Steel KP. (2023) Reversal of an existing hearing loss by gene activation in mutant mice. Proceedings of the National Academy of Sciences of the United States of America. 120: e2307355120 |
| Lachgar-Ruiz M, Morín M, Martelletti E, et al. (2023) Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants. Disease Models & Mechanisms |
| Lewis MA, Schulte J, Matthews L, et al. (2023) Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. Medrxiv : the Preprint Server For Health Sciences |
| Chiereghin C, Robusto M, Lewis MA, et al. (2023) In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear. Plos One. 18: e0273586 |