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

od Ingham, Neil J
Wydane w Bio Protoc (2019)

GABAergic Inhibition Controls Neural Gain in Inferior Colliculus Neurons Sensitive to Interaural Time Differences

od Ingham, Neil J., McAlpine, David
Wydane w J Neurosci (2005)

Enhancement of forward suppression begins in the ventral cochlear nucleus

od Ingham, Neil J., Itatani, Naoya, Bleeck, Stefan, Winter, Ian M.
Wydane w Brain Res (2016)

Hearing impairment due to Mir183/96/182 mutations suggests both loss-of-function and gain-of-function effects

od Lewis, Morag A., Di Domenico, Francesca, Ingham, Neil J., Prosser, Haydn M., Steel, Karen P.
Wydane w Dis Model Mech (2021)

Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice

od Martelletti, Elisa, Ingham, Neil J., Houston, Oliver, Pass, Johanna C., Chen, Jing, Marcotti, Walter, Steel, Karen P.
Wydane w Front Cell Neurosci (2020)

Functional analysis of candidate genes from genome-wide association studies of hearing

od Ingham, Neil J., Rook, Victoria, Di Domenico, Francesca, James, Elysia, Lewis, Morag A., Girotto, Giorgia, Buniello, Annalisa, Steel, Karen P.
Wydane w Hear Res (2020)

Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia

od Ebrahim, Seham, Ingham, Neil J., Lewis, Morag A., Rogers, Michael J.C., Cui, Runjia, Kachar, Bechara, Pass, Johanna C., Steel, Karen P.
Wydane w Cell Rep (2016)

S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse

od Ingham, Neil J., Carlisle, Francesca, Pearson, Selina, Lewis, Morag A., Buniello, Annalisa, Chen, Jing, Isaacson, Rivka L., Pass, Johanna, White, Jacqueline K., Dawson, Sally J., Steel, Karen P.
Wydane w Sci Rep (2016)

The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss

od Spiden, Sarah L., Bortolozzi, Mario, Di Leva, Francesca, de Angelis, Martin Hrabé, Fuchs, Helmut, Lim, Dmitry, Ortolano, Saida, Ingham, Neil J., Brini, Marisa, Carafoli, Ernesto, Mammano, Fabio, Steel, Karen P.
Wydane 2008

ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells

od Morozko, Eva L., Nishio, Ayako, Ingham, Neil J., Chandra, Rashmi, Fitzgerald, Tracy, Martelletti, Elisa, Borck, Guntram, Wilson, Elizabeth, Riordan, Gavin P., Wangemann, Philine, Forge, Andrew, Steel, Karen P., Liddle, Rodger A., Friedman, Thomas B., Belyantseva, Inna A.
Wydane w Hum Mol Genet (2015)

Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing

od Buniello, Annalisa, Ingham, Neil J, Lewis, Morag A, Huma, Andreea C, Martinez‐Vega, Raquel, Varela‐Nieto, Isabel, Vizcay‐Barrena, Gema, Fleck, Roland A, Houston, Oliver, Bardhan, Tanaya, Johnson, Stuart L, White, Jacqueline K, Yuan, Huijun, Marcotti, Walter, Steel, Karen P
Wydane w EMBO Mol Med (2016)

Mouse screen reveals multiple new genes underlying mouse and human hearing loss

od Ingham, Neil J., Pearson, Selina A., Vancollie, Valerie E., Rook, Victoria, Lewis, Morag A., Chen, Jing, Buniello, Annalisa, Martelletti, Elisa, Preite, Lorenzo, Lam, Chi Chung, Weiss, Felix D., Powis, Zӧe, Suwannarat, Pim, Lelliott, Christopher J., Dawson, Sally J., White, Jacqueline K., Steel, Karen P.
Wydane w PLoS Biol (2019)

Genome-wide Generation and Systematic Phenotyping of Knockout Mice Reveals New Roles for Many Genes

od White, Jacqueline K., Gerdin, Anna-Karin, Karp, Natasha A., Ryder, Ed, Buljan, Marija, Bussell, James N., Salisbury, Jennifer, Clare, Simon, Ingham, Neil J., Podrini, Christine, Houghton, Richard, Estabel, Jeanne, Bottomley, Joanna R., Melvin, David G., Sunter, David, Adams, Niels C., Tannahill, David, Logan, Darren W., MacArthur, Daniel G., Flint, Jonathan, Mahajan, Vinit B., Tsang, Stephen H., Smyth, Ian, Watt, Fiona M., Skarnes, William C., Dougan, Gordon, Adams, David J., Ramirez-Solis, Ramiro, Bradley, Allan, Steel, Karen P.
Wydane 2013

Deficiency for the Ubiquitin Ligase UBE3B in a Blepharophimosis-Ptosis-Intellectual-Disability Syndrome

od Basel-Vanagaite, Lina, Dallapiccola, Bruno, Ramirez-Solis, Ramiro, Segref, Alexandra, Thiele, Holger, Edwards, Andrew, Arends, Mark J., Miró, Xavier, White, Jacqueline K., Désir, Julie, Abramowicz, Marc, Dentici, Maria Lisa, Lepri, Francesca, Hofmann, Kay, Har-Zahav, Adi, Ryder, Edward, Karp, Natasha A., Estabel, Jeanne, Gerdin, Anna-Karin B., Podrini, Christine, Ingham, Neil J., Altmüller, Janine, Nürnberg, Gudrun, Frommolt, Peter, Abdelhak, Sonia, Pasmanik-Chor, Metsada, Konen, Osnat, Kelley, Richard I., Shohat, Mordechai, Nürnberg, Peter, Flint, Jonathan, Steel, Karen P., Hoppe, Thorsten, Kubisch, Christian, Adams, David J., Borck, Guntram
Wydane 2012

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction

od Bowl, Michael R., Simon, Michelle M., Ingham, Neil J., Greenaway, Simon, Santos, Luis, Cater, Heather, Taylor, Sarah, Mason, Jeremy, Kurbatova, Natalja, Pearson, Selina, Bower, Lynette R., Clary, Dave A., Meziane, Hamid, Reilly, Patrick, Minowa, Osamu, Kelsey, Lois, Tocchini-Valentini, Glauco P., Gao, Xiang, Bradley, Allan, Skarnes, William C., Moore, Mark, Beaudet, Arthur L., Justice, Monica J., Seavitt, John, Dickinson, Mary E., Wurst, Wolfgang, de Angelis, Martin Hrabe, Herault, Yann, Wakana, Shigeharu, Nutter, Lauryl M. J., Flenniken, Ann M., McKerlie, Colin, Murray, Stephen A., Svenson, Karen L., Braun, Robert E., West, David B., Lloyd, K. C. Kent, Adams, David J., White, Jacqui, Karp, Natasha, Flicek, Paul, Smedley, Damian, Meehan, Terrence F., Parkinson, Helen E., Teboul, Lydia M., Wells, Sara, Steel, Karen P., Mallon, Ann-Marie, Brown, Steve D. M.
Wydane w Nat Commun (2017)

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

od Simon, Michelle M, Greenaway, Simon, White, Jacqueline K, Fuchs, Helmut, Gailus-Durner, Valérie, Wells, Sara, Sorg, Tania, Wong, Kim, Bedu, Elodie, Cartwright, Elizabeth J, Dacquin, Romain, Djebali, Sophia, Estabel, Jeanne, Graw, Jochen, Ingham, Neil J, Jackson, Ian J, Lengeling, Andreas, Mandillo, Silvia, Marvel, Jacqueline, Meziane, Hamid, Preitner, Frédéric, Puk, Oliver, Roux, Michel, Adams, David J, Atkins, Sarah, Ayadi, Abdel, Becker, Lore, Blake, Andrew, Brooker, Debra, Cater, Heather, Champy, Marie-France, Combe, Roy, Danecek, Petr, di Fenza, Armida, Gates, Hilary, Gerdin, Anna-Karin, Golini, Elisabetta, Hancock, John M, Hans, Wolfgang, Hölter, Sabine M, Hough, Tertius, Jurdic, Pierre, Keane, Thomas M, Morgan, Hugh, Müller, Werner, Neff, Frauke, Nicholson, George, Pasche, Bastian, Roberson, Laura-Anne, Rozman, Jan, Sanderson, Mark, Santos, Luis, Selloum, Mohammed, Shannon, Carl, Southwell, Anne, Tocchini-Valentini, Glauco P, Vancollie, Valerie E, Westerberg, Henrik, Wurst, Wolfgang, Zi, Min, Yalcin, Binnaz, Ramirez-Solis, Ramiro, Steel, Karen P, Mallon, Ann-Marie, de Angelis, Martin Hrabě, Herault, Yann, Brown, Steve DM
Wydane 2013