Cochlear Neuropathy and Hearing Loss Mechanisms

Displaying 1 - 17 of 17CSV
Weinstein, H. N. W., Tucker, L. H., Grewal, M. R., Denham, M. W., Brewster, K. K., & Golub, J. S. (2025). The Association Between Hearing Loss and Depression in a Large Electronic Health Record System. Otolaryngology–Head and Neck Surgery. Portico. https://doi.org/10.1002/ohn.1136
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Bharadwaj, T., Acharya, A., Khan, F. U., Khan, S., Ullah, I., Schrauwen, I., Ahmad, W., & Leal, S. M. (2024). THBS1 is a new autosomal recessive non-syndromic hearing impairment gene. BMC Medical Genomics, 17(1). https://doi.org/10.1186/s12920-024-02060-w
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Pennington‐FitzGerald, W., Waring, N. A., Hamiter, M., Kuhlmey, M., & Kim, A. H. (2024). Impact of Cochlear Implant Electrode Array Design on Post‐Op Speech Perception. Otolaryngology–Head and Neck Surgery. Portico. https://doi.org/10.1002/ohn.995
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Denham, M. W., Tucker, L. H., Gorroochurn, P., & Golub, J. S. (2024). Hearing Loss and Reduced Income Growth: A Longitudinal Socioeconomic Analysis. Otolaryngology–Head and Neck Surgery. Portico. https://doi.org/10.1002/ohn.797
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Alter, I. L., Tucker, L. H., Dragon, J. M., Grewal, M. R., Saperstein, A., Stroup, T. S., Medalia, A. A., & Golub, J. S. (2024). National Cohort Data Suggests an Association Between Serious Mental Illness and Audiometric Hearing Loss. Otolaryngology–Head and Neck Surgery. Portico. https://doi.org/10.1002/ohn.763
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Leong, S., Teh, B. M., Duong, T., Hu, D., Chui, A., Chen, J. S., Sisti, M. B., Wang, T. J. C., Zanotto, D., & Lalwani, A. K. (2023). Instrumented insoles for assessment of gait in patients with vestibular schwannoma. Wearable Technologies, 4. https://doi.org/10.1017/wtc.2023.11
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Tong, C., Moayedi, Y., & Lumpkin, E. A. (2024). Merkel cells and keratinocytes in oral mucosa are activated by mechanical stimulation. Physiological Reports, 12(2). Portico. https://doi.org/10.14814/phy2.15826
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Naderi, E., Cornejo-Sanchez, D. M., Li, G., Schrauwen, I., Wang, G. T., Dewan, A. T., & Leal, S. M. (2023). The genetic contribution of the X chromosome in age-related hearing loss. Frontiers in Genetics, 14. https://doi.org/10.3389/fgene.2023.1106328
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Chen, N., Lee, H., Kim, A. H., Liu, P.-K., Kang, E. Y.-C., Tseng, Y.-J., Seo, G. H., Khang, R., Liu, L., Chen, K.-J., Wu, W.-C., Hsiao, M.-C., & Wang, N.-K. (2022). Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigmentosa. BMC Ophthalmology, 22(1). https://doi.org/10.1186/s12886-022-02659-6
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Tawalbeh, M., Aburizeg, D., Abu Alragheb, B. O., Alaqrabawi, W. S., Dardas, Z., Srour, L., Altarayra, B. H., Zayed, A. A., El Omari, Z., & Azab, B. (2022). SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management. Genes, 13(12), 2192. https://doi.org/10.3390/genes13122192
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Adadey, S. M., Aboagye, E. T., Esoh, K., Acharya, A., Bharadwaj, T., Lin, N. S., Amenga-Etego, L., Awandare, G. A., Schrauwen, I., Leal, S. M., & Wonkam, A. (2022). A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana. BMC Medical Genomics, 15(1). https://doi.org/10.1186/s12920-022-01391-w
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Tavernier, L. J. M., Vanpoucke, T., Schrauwen, I., Van Camp, G., & Fransen, E. (2022). Targeted Resequencing of Otosclerosis Patients from Different Populations Replicates Results from a Previous Genome-Wide Association Study. Journal of Clinical Medicine, 11(23), 6978. https://doi.org/10.3390/jcm11236978
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Wonkam, A., Adadey, S. M., Schrauwen, I., Aboagye, E. T., Wonkam-Tingang, E., Esoh, K., Popel, K., Manyisa, N., Jonas, M., deKock, C., Nembaware, V., Cornejo Sanchez, D. M., Bharadwaj, T., Nasir, A., Everard, J. L., Kadlubowska, M. K., Nouel-Saied, L. M., Acharya, A., Quaye, O., … Leal, S. M. (2022). Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes. Communications Biology, 5(1). https://doi.org/10.1038/s42003-022-03326-8
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Martinez-Amezcua, P., Dooley, E. E., Reed, N. S., Powell, D., Hornikel, B., Golub, J. S., Pettee Gabriel, K., & Palta, P. (2022). Association of Hearing Impairment and 24-Hour Total Movement Activity in a Representative Sample of US Adults. JAMA Network Open, 5(3), e222983. https://doi.org/10.1001/jamanetworkopen.2022.2983
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Bharadwaj, T., Schrauwen, I., Acharya, A., Nouel‐Saied, L. M., Väisänen, M., Kraatari, M., Rahikkala, E., Jarvela, I., Kotimäki, J., & Leal, S. M. (2022). Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. Molecular Genetics & Genomic Medicine, 10(3). Portico. https://doi.org/10.1002/mgg3.1866
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