Neil J. Ingham

The paper investigates the role of Zfp719 in hearing maintenance in mice, finding that its mutation leads to progressive hearing loss and outer hair cell degeneration.

The paper introduces a non-invasive test to distinguish stria vascularis dysfunction from other causes of hearing loss in mice, using inter-trial coherence in auditory brainstem responses.

This study identifies ESRRG as essential for normal auditory innervation and hearing by showing that its loss causes early-onset hearing loss and synaptic defects in mice.

This study shows that a specific type of hearing loss in mice can be reversed by reactivating the Spns2 gene within a critical period, restoring auditory function and protecting hair cells.

The paper identifies and characterizes spontaneous mutations causing deafness in mice from a targeted knockout program, showing these mutations are a common side effect of intensive breeding.

This paper identifies Klhl18 mutant mice with low-frequency progressive hearing loss due to inner hair cell dysfunction, showing abnormal stereocilia and normal outer hair cell function.

This study investigates the effects of Mir183/96/182 mutations on hearing, finding that loss of these microRNAs causes deafness, while their mutations can lead to both loss and gain of function effects.