ScholarIQanswers from OpenAlex
Hearing, Cochlea, Tinnitus, Genetics
TopicLeading institutions, researchers & key papers
Hearing, Cochlea, Tinnitus, Genetics is a topic indexed in ScholarIQ from OpenAlex.
What is known about Hearing, Cochlea, Tinnitus, Genetics?
ScholarIQrecord summary
This cluster of papers explores the mechanisms and consequences of cochlear neuropathy, hearing loss, and related conditions such as tinnitus. It covers topics such as hair cell function, inner ear development, noise-induced damage, otoacoustic emissions, neural plasticity, connexin mutations, and the overall auditory system.
How many works does Hearing, Cochlea, Tinnitus, Genetics have?
ScholarIQindexed works
Hearing, Cochlea, Tinnitus, Genetics has 440 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
What is the OpenAlex record for Hearing, Cochlea, Tinnitus, Genetics?
ScholarIQopenalex
The OpenAlex for Hearing, Cochlea, Tinnitus, Genetics is on the source record.
What are the most-cited papers on Hearing, Cochlea, Tinnitus, Genetics?
ScholarIQmost cited works
Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier
M. Charles Liberman, Jiangang Gao, David Z. Z. He, Xudong Wu, Shuping Jia, Jianping Zuo
The functional neuroanatomy of tinnitus
Alan H. Lockwood, Richard Salvi, Mary Lou Coad, M. L. Towsley, David S. Wack, B. W. Murphy
State of the States
Kathryn H. Arehart, Christine Yoshinaga‐Itano, Vickie Thomson, Sandra Abbott Gabbard, Arlene Stredler Brown
Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss
Christina Sloan-Heggen, Amanda O. Bierer, A. Eliot Shearer, Diana L. Kolbe, Carla Nishimura, Kathy L. Frees, Sean S. Ephraim, Seiji B. Shibata, Kevin T. Booth, Colleen A. Campbell, Paul T. Ranum, Amy E. Weaver, E. Ann Black-Ziegelbein, Donghong Wang, Héla Azaiez, Richard J. Smith
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, Sandrine Marlin, Françoise Denoyelle, J Waligora, Małgorzata Mueller‐Malesińska, Agneszka Pollak, Rafał Płoski, Alessandra Murgia, Eva Orzan, Pierangela Castorina, Umberto Ambrosetti, Ewa Nowakowska-Szyrwińska, Jerzy Bal, Wojciech Wiszniewski, Andreas Janecke, Doris Nekahm-Heis, Pavel Seeman, O. Bendová, Margaret A. Kenna, Anna Frangulov, Heidi L. Rehm, Mustafa Tekin, Armağan İncesulu, Hans‐Henrik M. Dahl, Desirée du Sart, Lucy Jenkins, Deirdre Lucas, Maria Bitner‐Glindzicz, Karen B. Avraham, Zippora Brownstein, Ignacio del Castillo, Felipe Moreno, Nikolaus Blin, Markus Pfister, István Sziklai, Tímea Tóth, Philip M. Kelley, Edward Cohn, Lionel Van Maldergem, Pascale Hilbert, Anne‐Françoise Roux, M. Mondain, Lies H. Hoefsloot, Cor W. R. J. Cremers, Tuija Löppönen, Heikki Löppönen, Agnete Parving, Karen Grønskov, Iris Schrijver, Joseph Roberson, Francesca Gualandi, Alessandro Martini, Geneviève Lina‐Granade, Nathalie Pallarès-Ruiz, Céu Correia, Graça Fialho, Kim Cryns, Nele Hilgert, Paul Van de Heyning, Carla Nishimura, Richard J. Smith, Guy Van Camp
Where is Hearing, Cochlea, Tinnitus, Genetics research published, and who funds it?
ScholarIQvenues & funding sources
TOP JOURNALS
TOP FUNDERS
National Science Foundation—
NIH—
Wellcome Trust—
European Research Council—
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How much of the research on Hearing, Cochlea, Tinnitus, Genetics is open access?
ScholarIQopen access share
27%OPEN ACCESS