Publications by authors named "Neil Ingham"

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Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism.
Hormos Salimi Dafsari, Celine Deneubourg, Kritarth Singh, Reza Maroofian, Zita Suprenant, Neil J Ingham

Ann Neurol· November 2025

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Non-invasive testing to diagnose the underlying auditory pathology of hearing impairment.
Neil J Ingham, Karen P Steel

Hear Res· October 2025

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Low level of expression of known deafness genes Kcne1, Kcnj10 or Col4a3 is sufficient to maintain hearing in mice.
Darcey A Kirwin, Nina Treder, Elisa Martelletti, Daniel R Pentland, Rechal Kumar, Neil J Ingham

Hear Res· September 2025

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A machine-learning-based approach to predict early hallmarks of progressive hearing loss.
Federico Ceriani, Joshua Giles, Neil J Ingham, Jing-Yi Jeng, Morag A Lewis

Hear Res· August 2025

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Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease.
Aara Patel, Valda Pauzuolyte, Neil J Ingham, Yeh Chwan Leong, Wolfgang Berger

Proc Natl Acad Sci U S A· December 2024

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Two new mouse alleles of Ocm and Slc26a5.
Marìa Lachgar-Ruiz, Neil J Ingham, Elisa Martelletti, Jing Chen, Elysia James

Hear Res· October 2024

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A new mutation of Sgms1 causes gradual hearing loss associated with a reduced endocochlear potential.
Jing Chen, Morag A Lewis, Alisa Wai, Lucia Yin, Sally J Dawson, Neil J Ingham

Hear Res· September 2024

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Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease.
Valda Pauzuolyte, Aara Patel, James R Wawrzynski, Neil J Ingham, Yeh Chwan Leong

EMBO Mol Med· October 2023

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Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants.
María Lachgar-Ruiz, Matías Morín, Elisa Martelletti, Neil J Ingham, Lorenzo Preite

Dis Model Mech· August 2023

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Reversal of an existing hearing loss by gene activation in mutant mice.
Elisa Martelletti, Neil J Ingham, Karen P Steel

Proc Natl Acad Sci U S A· August 2023

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The Effect of a Mutation on Hearing and Lipid Content of the Inner Ear.
Rafael M Kochaj, Elisa Martelletti, Neil J Ingham, Annalisa Buniello, Bebiana C Sousa

Cells· October 2022

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Mutations in encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.
Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar, Mohammad Faraz Zafeer, Clemer Abad, Neil J Ingham

Proc Natl Acad Sci U S A· June 2022

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Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
Morag A Lewis, Neil J Ingham, Jing Chen, Selina Pearson, Francesca Di Domenico

BMC Biol· March 2022

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The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention.
Dale Bryant, Valda Pauzuolyte, Neil J Ingham, Aara Patel, Waheeda Pagarkar

JCI Insight· February 2022

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Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss.
Neil J Ingham, Navid Banafshe, Clarisse Panganiban, Julia L Crunden, Jing Chen

PLoS One· November 2021

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Hearing impairment due to mutations suggests both loss and gain of function effects.
Morag A Lewis, Francesca Di Domenico, Neil J Ingham, Haydn M Prosser, Karen P Steel

Dis Model Mech· December 2020

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Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice.
Elisa Martelletti, Neil J Ingham, Oliver Houston, Johanna C Pass, Jing Chen

Front Cell Neurosci· September 2020

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Functional analysis of candidate genes from genome-wide association studies of hearing.
Neil J Ingham, Victoria Rook, Francesca Di Domenico, Elysia James, Morag A Lewis

Hear Res· March 2020

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Evoked Potential Recordings of Auditory Brainstem Activity in the Mouse: An Optimized Method for the Assessment of Hearing Function of Mice.
Neil J Ingham

Bio Protoc· December 2019

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Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
Neil J Ingham, Selina A Pearson, Valerie E Vancollie, Victoria Rook, Morag A Lewis

PLoS Biol· April 2019

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A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Michael R Bowl, Michelle M Simon, Neil J Ingham, Simon Greenaway, Luis Santos

Nat Commun· October 2017

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On the role of ephrinA2 in auditory function.
Neil J Ingham, Karen P Steel, Uwe Drescher

Hear Res· July 2017

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S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.
Neil J Ingham, Francesca Carlisle, Selina Pearson, Morag A Lewis, Annalisa Buniello

Sci Rep· July 2016

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Enhancement of forward suppression begins in the ventral cochlear nucleus.
Neil J Ingham, Naoya Itatani, Stefan Bleeck, Ian M Winter

Brain Res· May 2016

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Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia.
Seham Ebrahim, Neil J Ingham, Morag A Lewis, Michael J C Rogers, Runjia Cui

Cell Rep· May 2016

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