Neil J. Ingham

King's College London — United Kingdom

Neuroscience · Life Sciences

26h-index2.9kcitations73works2.12yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(41), Hearing Loss and Rehabilitation(19), RNA regulation and disease(10), Neural dynamics and brain function(9), RNA and protein synthesis mechanisms(7)

Publications73 total

Mutations in the Key Autophagy Tethering Factor <scp>EPG5</scp> Link Neurodevelopmental and Neurodegenerative Disorders Including Early‐Onset Parkinsonism
Annals of Neurology·2025· 3 citedOpen Access
Non-invasive testing to diagnose the underlying auditory pathology of hearing impairment
Hearing Research·2025Open Access
A non-invasive test for stria vascularis dysfunction
2025Open Access
Low level of expression of known deafness genes Kcne1, Kcnj10 or Col4a3 is sufficient to maintain hearing in mice
Hearing Research·2025Open Access
A machine-learning-based approach to predict early hallmarks of progressive hearing loss
Hearing Research·2025· 1 citedOpen Access
Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease
Proceedings of the National Academy of Sciences·2024· 5 citedOpen Access
Two new mouse alleles of Ocm and Slc26a5
Hearing Research·2024· 2 citedOpen Access
A new mutation of Sgms1 causes gradual hearing loss associated with a reduced endocochlear potential
Hearing Research·2024· 5 citedOpen Access
Mutations in EPG5 are associated with a wide spectrum of neurodevelopmental and neurodegenerative disorders
2024· 3 citedOpen Access
Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease
EMBO Molecular Medicine·2023· 16 citedOpen Access
Reversal of an existing hearing loss by gene activation in <i>Spns2</i> mutant mice
Proceedings of the National Academy of Sciences·2023· 6 citedOpen Access
Insights into the pathophysiology of DFNA44 hearing loss associated with <i>CCDC50</i> frameshift variants
Disease Models & Mechanisms·2023· 3 citedOpen Access
Reversal of an existing hearing loss in <i>Spns2</i> mutant mice
2023Open Access
The Effect of a Pex3 Mutation on Hearing and Lipid Content of the Inner Ear
Cells·2022· 8 citedOpen Access
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice
Proceedings of the National Academy of Sciences·2022· 7 citedOpen Access
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme
BMC Biology·2022· 5 citedOpen Access
The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention
JCI Insight·2022· 12 citedOpen Access
Additional file 2 of Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme
Figshare·2022Open Access
Additional file 3 of Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme
Figshare·2022Open Access
Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss
PLoS ONE·2021· 16 citedOpen Access
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Frequent Co-authors

Karen P. Steel(33), Morag A. Lewis(12), Jacqueline K. White(9), Selina Pearson(9), David J. Adams(7), Jing Chen(7), Annalisa Buniello(5), Elisa Martelletti(5), Walter Marcotti(5), Johanna Pass(5), Sally K. Thornton(5), D.J. Withington(5), Jeanne Estabel(4), Anna-Karin Gerdin(4), Valerie E. Vancollie(4), Ramiro Ramírez‐Solis(4), David McAlpine(4), Stefan Bleeck(4), Ian M. Winter(4), Thomas Keane(3)