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Items: 1 to 20 of 500

1.
Focal Unilateral Palatal Myoclonus Causing Objective Clicking Tinnitus without Uvula Elevation Diagnosed by Concurrent Auscultation
Chindhuri Selvadurai, Sara Maguire Schaefer
J Mov Disord. 2020 Sep; 13(3): 223–224. Published online 2020 Jul 14. doi: 10.14802/jmd.20010
PMCID:
PMC7502295
ArticlePDF–111K
2.
A Case of Spontaneous Temporomandibular Joint Herniation into the External Auditory Canal with Clicking Sound
Tae Hyun Kim, Sun Kyu Lee, Su Jin Kim, Jae Yong Byun
Korean J Audiol. 2013 Sep; 17(2): 90–93. Published online 2013 Sep 24. doi: 10.7874/kja.2013.17.2.90
PMCID:
PMC3936545
ArticlePDF–2.2M
3.
A Systematic Review on the Genetic Contribution to Tinnitus
Patricia Perez-Carpena, Jose A. Lopez-Escamez, Álvaro Gallego-Martinez
J Assoc Res Otolaryngol. 2024 Feb; 25(1): 13–33. Published online 2024 Feb 9. doi: 10.1007/s10162-024-00925-6
PMCID:
PMC10907330
ArticlePDF–1.6M
4.
Causal Associations of Genetically Determined Tinnitus With Neuroimaging Traits: Evidence From a Mendelian Randomization Study
Jing Sun, Xinghao Wang, Jia Li, Tingting Zhang, Qian Chen, Wenjuan Liu, Linkun Cai, Pengfei Zhao, Zhenghan Yang, Junhua Pan, Zhenchang Wang, Han Lv
Ear Hear. 2024 Mar-Apr; 45(2): 370–377. Published online 2023 Oct 6. doi: 10.1097/AUD.0000000000001429
PMCID:
PMC10868673
ArticlePDF–936K
5.
Patient-reported measures of tinnitus for individuals with neurofibromatosis type 2–related schwannomatosis: Recommendations for clinical trials
Heather L Thompson, Jane Grabowski, Barbara Franklin, Kimberley S Koetsier, D Bradley Welling
Clin Trials. 2024 Feb; 21(1): 18–28. Published online 2024 Feb 6. doi: 10.1177/17407745231217279
PMCID:
PMC10865763
ArticlePDF–1.4M
6.
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians
Ishan Sunilkumar Bhatt, Raquel Dias, Ali Torkamani
Otol Neurotol. Author manuscript; available in PMC 2024 Feb 12.
Published in final edited form as: Otol Neurotol. 2021 Oct 1; 42(9): e1203–e1212. doi: 10.1097/MAO.0000000000003279
PMCID:
PMC10860185
ArticlePDF–837K
7.
Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease
Alba Escalera-Balsera, Alberto M. Parra-Perez, Alvaro Gallego-Martinez, Lidia Frejo, Juan Martin-Lagos, Victoria Rivero de Jesus, Paz Pérez-Vázquez, Patricia Perez-Carpena, Jose A. Lopez-Escamez
Genes (Basel) 2024 Jan; 15(1): 22. Published online 2023 Dec 22. doi: 10.3390/genes15010022
PMCID:
PMC10815708
ArticlePDF–2.2M
8.
Genetic architecture distinguishes tinnitus from hearing loss
Royce E. Clifford, Adam X. Maihofer, Chris Chatzinakos, Jonathan R. I. Coleman, Nikolaos P. Daskalakis, Marianna Gasperi, Kelleigh Hogan, Elizabeth A. Mikita, Murray B. Stein, Catherine Tcheandjieu, Francesca Telese, Yanning Zuo, Allen F. Ryan, Caroline M. Nievergelt
Nat Commun. 2024; 15: 614. Published online 2024 Jan 19. doi: 10.1038/s41467-024-44842-x
PMCID:
PMC10799010
ArticlePDF–2.2M
9.
Candidate Key Proteins in Tinnitus: A Bioinformatic Study of Synaptic Transmission in Spiral Ganglion Neurons
Johann Gross, Marlies Knipper, Birgit Mazurek
Cell Mol Neurobiol. 2023; 43(8): 4189–4207. Published online 2023 Sep 22. doi: 10.1007/s10571-023-01405-w
PMCID:
PMC10661836
ArticlePDF–4.7M
10.
Types of Inheritance and Genes Associated with Familial Meniere Disease
Alberto M. Parra-Perez, Jose A. Lopez-Escamez
J Assoc Res Otolaryngol. 2023 Jun; 24(3): 269–279. Published online 2023 Apr 6. doi: 10.1007/s10162-023-00896-0
PMCID:
PMC10335989
ArticlePDF–1.6M
11.
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress
Erik Fransen, Laura L.M. Cassiers, Viktoriia Chubar, Annick Gilles, Vincent Van Rompaey, Ilse van der Werf, Paul Van de Heyning, Stephan Claes, Bernard Sabbe, R. Frank Kooy, Filip Van Den Eede
Psychiatr Genet. 2023 Aug; 33(4): 134–144. Published online 2023 May 4. doi: 10.1097/YPG.0000000000000339
PMCID:
PMC10325559
ArticlePDF–838K
12.
A genome-wide association study of tinnitus reveals shared genetic links to neuropsychiatric disorders
Ishan Sunilkumar Bhatt, Nicholas Wilson, Raquel Dias, Ali Torkamani
Sci Rep. 2022; 12: 22511. Published online 2022 Dec 29. doi: 10.1038/s41598-022-26413-6
PMCID:
PMC9800371
ArticlePDF–1.9M
13.
Pharmacogenomics of cisplatin‐induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy
Xindi Zhang, Matthew R. Trendowski, Emma Wilkinson, Mohammad Shahbazi, Paul C. Dinh, Megan M. Shuey, Regeneron Genetics Center, Darren R. Feldman, Robert J. Hamilton, David J. Vaughn, Chunkit Fung, Christian Kollmannsberger, Robert Huddart, Neil E. Martin, Victoria A. Sanchez, Robert D. Frisina, Lawrence H. Einhorn, Nancy J. Cox, Lois B. Travis, M. Eileen Dolan
Cancer Med. 2022 Jul; 11(14): 2801–2816. Published online 2022 Mar 23. doi: 10.1002/cam4.4644
PMCID:
PMC9302309
ArticlePDF–6.0M
14.
The Road Traveled and Journey Ahead for the Genetics and Genomics of Tinnitus
Barbara Vona
Mol Diagn Ther. 2022; 26(2): 129–136. Published online 2022 Feb 15. doi: 10.1007/s40291-022-00578-2
PMCID:
PMC8942952
ArticlePDF–760K
15.
Effects of two inhibitors of metabolic glutamate receptor 5 on expression of endogenous homer scaffold protein 1 in the auditory cortex of mice with tinnitus
Weiwei Yan, Hongfei Zhu, Bianbian Yu, Xin Ma, Hang Liang, Shuyan Zhao, Kebin Deng
Bioengineered. 2021; 12(1): 7145–7153. Published online 2021 Sep 21. doi: 10.1080/21655979.2021.1979354
PMCID:
PMC8806735
ArticlePDF–1.2M
16.
Hearing Loss and Tinnitus: Association Studies for Complex Hearing Disorders In Mouse and Man
Ely Cheikh Boussaty, Rick Adam Friedman, Million Veteran Program, Royce E. Clifford
Hum Genet. Author manuscript; available in PMC 2023 Apr 1.
Published in final edited form as: Hum Genet. 2022 Apr; 141(3-4): 981–990. Published online 2021 Jul 27. doi: 10.1007/s00439-021-02317-9
PMCID:
PMC8792513
ArticlePDF–540K
17.
Analysis of Studies in Tinnitus-Related Gene Research
Zhi-cheng Li, Bi-xing Fang, Lian-xiong Yuan, Ke Zheng, Shi-xin Wu, Nanbert Zhong, Xiang-li Zeng
Noise Health. 2021 Oct-Dec; 23(111): 95–107. Published online 2021 Dec 28. doi: 10.4103/nah.nah_57_21
PMCID:
PMC8772442
Article
18.
A KCNQ4 c.546C>G Genetic Variant Associated with Late Onset Non-Syndromic Hearing Loss in a Taiwanese Population
Ting-Ting Yen, I-Chieh Chen, Men-Wei Hua, Chia-Yi Wei, Kai-Hsiang Shih, Jui-Lin Li, Ching-Heng Lin, Tzu-Hung Hsiao, Yi-Ming Chen, Rong-San Jiang
Genes (Basel) 2021 Nov; 12(11): 1711. Published online 2021 Oct 27. doi: 10.3390/genes12111711
PMCID:
PMC8618107
ArticlePDF–1.1M
19.
Clinical and Genetic Risk Factors for Radiation-Associated Ototoxicity: A Report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort
Matthew R. Trendowski, Jessica L. Baedke, Yadav Sapkota, Lois B. Travis, Xindi Zhang, Omar El Charif, Heather E. Wheeler, Wendy M. Leisenring, Leslie L. Robison, Melissa M. Hudson, Lindsay M. Morton, Kevin C. Oeffinger, Rebecca M. Howell, Gregory T. Armstrong, Smita Bhatia, M. Eileen Dolan
Cancer. Author manuscript; available in PMC 2022 Nov 1.
Published in final edited form as: Cancer. 2021 Nov 1; 127(21): 4091–4102. Published online 2021 Jul 19. doi: 10.1002/cncr.33775
PMCID:
PMC8516694
ArticlePDF–898K
20.
Genome-wide association study identifies new loci associated with noise-induced tinnitus in Chinese populations
Chengyong Xie, Yuguang Niu, Jie Ping, Yahui Wang, Chenning Yang, Yuanfeng Li, Gangqiao Zhou
BMC Genom Data. 2021; 22: 31. Published online 2021 Sep 6. doi: 10.1186/s12863-021-00987-y
PMCID:
PMC8420059
ArticlePDF–1.3M

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