Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 618 Records) |
Query Trace: Hearing and GJB2[original query] |
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Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment. The Journal of molecular diagnostics : JMD 2023 9 . Yu-Ting Chiang, Pei-Hsuan Lin, Ming-Yu Lo, Hsin-Lin Chen, Chen-Yu Lee, Cheng-Yu Tsai, Yin-Hung Lin, Shih-Feng Tsai, Tien-Chen Liu, Chuan-Jen Hsu, Pei-Lung Chen, Jacob Shu-Jui Hsu, Chen-Chi |
Follow-up of infants with mild-to-moderate sensorineural hearing loss over three years. International journal of pediatric otorhinolaryngology 2023 8 173 111697. Yanling Hu, Zhongfang Xia, Ping Ch |
GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population. Ear and hearing 2023 6 . Ting-Ting Yen, I-Chieh Chen, Sudi Cho, Ting-Gang Chang, Kai-Hsiang Shih, Men-Wei Hua, Jui-Lin Li, Chiann-Yi Hsu, Tzu-Hung Hsiao, Yi-Ming Ch |
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia). Genes 2023 5 14 (5): . Vera G Pshennikova, Fedor M Teryutin, Alexandra M Cherdonova, Tuyara V Borisova, Aisen V Solovyev, Georgii P Romanov, Igor V Morozov, Alexander A Bondar, Olga L Posukh, Sardana A Fedorova, Nikolay A Barashk |
Programming Levels and Speech Perception in Pediatric Cochlear Implant Recipients With Enlarged Vestibular Aqueduct or GJB2 Mutation. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2023 5 44 (5): e273-e280. Kelly N Jahn, Charlotte Morse-Fortier, Amanda M Griffin, David Faller, Michael S Cohen, Margaret A Kenna, Elizabeth Doney, Julie G Arenbe |
Genetic Underpinnings and Audiological Characteristics in Children With Unilateral Sensorineural Hearing Loss. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2023 5 . Chen-Yu Lee, Pei-Hsuan Lin, Yu-Ting Chiang, Cheng-Yu Tsai, Shu-Yu Yang, You-Mei Chen, Chao-Hsuan Li, Chun-Yi Lu, Tien-Chen Liu, Chuan-Jen Hsu, Pei-Lung Chen, Jacob Shujui Hsu, Chen-Chi |
Preimplantation genetic testing for hereditary hearing loss in Chinese population. Journal of assisted reproduction and genetics 2023 4 . Bi Qingling, Huang Shasha, Wang Hui, Gao Xue, Ma Minyue, Han Mingyu, Lu Sijia, Kang Dongyang, Nourbakhsh Aida, Yan Denise, Blanton Susan, Liu Xuezhong, Yuan Yongyi, Yao Yuanqing, Dai |
Analysis of GJB2 gene mutations spectrum and the characteristics of individuals with c.109G>A in Western Guangdong. Molecular genetics & genomic medicine 2023 4 e2185. Shaoming Liang, Weihong Li, Zhichao Chen, Shimin Yuan, Zhao Wa |
Optimized concurrent hearing and genetic screening in Beijing, China: A cross-sectional study. Bioscience trends 2023 4 . Wen Cheng, Yang Xiaozhe, Cheng Xiaohua, Zhang Wei, Li Yichen, Wang Jing, Wang Chuan, Ruan Yu, Zhao Liping, Lu Hongli, Li Yingxin, Bai Yue, Yu Yiding, Li Yue, Xie Jinge, Qi Bei-Er, En Hui, Liu Hui, Fu Xinxing, Huang Lihui, Han Dem |
Analysis of SLC26A4 Gene in Individuals with Non Syndromic Hearing Impairment in Relation with GJB2 Associated Mutations. Avicenna journal of medical biotechnology 2023 4 15 (2): 124-127. Rajalakshmi Krishna, Thirunavukkarasu Jayakumar, Vikraman Meenu Ambika, Maruthy Santosh, Sylvester Charles, Kundapur Raje |
Novel WFS1 mutations in patients with low-to-middle frequency hearing loss. International journal of pediatric otorhinolaryngology 2023 3 167 111484. Guo Luo, Gu Xiaodong, Sun Qin, Zhang Yike, Li Huawei, Du Qia |
Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2023 3 . Salame Malak, Bonnet Crystel, Moctar Ely Cheikh Mohamed, Brahim Selma Mohamed, Dedy Abdallahi, Vetah Ledour Abdel, Veten Fatimetou, Hamed Cheikh Tijani, Petit Christine, Houmeida Ahm |
Association Between Susceptibility to SSHL and Single Nucleotide Polymorphisms at the rs2228612 Locus of the DNMT1 Gene and the rs5570459 Locus of the GJB2 Gene. Alternative therapies in health and medicine 2023 2 . Zhang Yanyan, Liu Hua, Song Yang, Liu Ning, Yao Cunj |
Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up. International journal of molecular sciences 2023 12 24 (23): . Aki Sakata, Akinori Kashio, Misaki Koyama, Shinji Urata, Hajime Koyama, Tatsuya Yamaso |
Next-generation sequencing for genetic testing of hearing loss populations. Clinica chimica acta; international journal of clinical chemistry 2023 12 552 117693. Lulu Wang, Gang Liu, Dingyuan Ma, Huasha Zeng, Yuguo Wang, Chunyu Luo, Jingjing Zhang, Zhengfeng |
Carrier screening for present disease prevalence and recessive genetic disorder in Taiwanese population. Journal of human genetics 2023 12 . Li Shan Chen, Cheng Wei Yu, Wei Jiun Li, Wen Chi Hsieh, Yi Ping |
Genetic screening of 15 hearing loss variants in 77,647 neonates with clinical follow-up. Molecular genetics & genomic medicine 2023 12 e2324. Lin Kun, Huang Jiexiang, Lin Hua, Han Junlin, Ruan Yijun, Zhang Lixian, Chen Mingqi |
Genotypic and Allelic Frequencies of GJB2 Variants and Features of Hearing Phenotypes in the Chinese Population of the Dongfeng-Tongji Cohort. Genes 2023 11 14 (11): . Lanlai Yuan, Xiaohui Wang, Xiaozhou Liu, Sen Chen, Weijia Kong, Meian He, Yu S |
Novel Pathogenic Variants in the Gene Encoding Stereocilin (STRC) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects. Biomedicines 2023 11 11 (11): . María Domínguez-Ruiz, Laura Ruiz-Palmero, Paula I Buonfiglio, Irene García-Vaquero, Elena Gómez-Rosas, Marina Goñi, Manuela Villamar, Matías Morín, Miguel A Moreno-Pelayo, Ana B Elgoyhen, Francisco J Del Castillo, Viviana Dalamón, Ignacio Del Castil |
Genetic analysis of 106 sporadic cases with hearing loss in the UAE population. Human genomics 2024 6 18 (1): 59. Abdelaziz Tlili, Mona Mahfood, Abdullah Al Mutery, Jihen Chouch |
Whole Exome Sequencing of Non-Syndromic Hearing Loss Patients. Iranian journal of public health 2024 6 53 (2): 453-461. Hossein Naddafnia, Zahra Noormohammadi, Shiva Irani, Iman Salahshoorif |
Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia. Croatian medical journal 2024 6 65 (3): 198-208. Ivona Sansovi?, Ana-Maria Meaši?, Adriana Bobinec, Leona Morožin Pohovski, Ljubica Odak, Katarina Vulin, Bernarda Lozi?, Mijana Kero, Sanda Huljev Frkovi?, Silvija Pušelj |
Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants. Scientific reports 2024 5 14 (1): 10596. Keita Tsukada, Shin-Ya Nishio, Yutaka Takumi, Shin-Ichi Usa |
Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing. Molecular biology reports 2024 5 51 (1): 662. Nahid Rezaie, Nader Mansour Samaei, Morteza Oladna |
Machine learning-based longitudinal prediction for GJB2-related sensorineural hearing loss. Computers in biology and medicine 2024 5 176 108597. Pey-Yu Chen, Ta-Wei Yang, Yi-Shan Tseng, Cheng-Yu Tsai, Chiung-Szu Yeh, Yen-Hui Lee, Pei-Hsuan Lin, Ting-Chun Lin, Yu-Jen Wu, Ting-Hua Yang, Yu-Ting Chiang, Jacob Shu-Jui Hsu, Chuan-Jen Hsu, Pei-Lung Chen, Chen-Fu Chou, Chen-Chi |
Unveiling a novel GJB2 dominant K22T mutation in a Chinese family with hearing loss. Acta biochimica et biophysica Sinica 2024 5 . Haiting Ji, Yilai Shu, Huawei |
Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families. The Journal of molecular diagnostics : JMD 2024 4 . Bo Gao, Yi Jiang, Mingyu Han, Xiaowen Ji, Dejun Zhang, Lihua Wu, Xue Gao, Shasha Huang, Chaoyue Zhao, Yu Su, Suyan Yang, Xin Zhang, Na Liu, Lu Han, Lihai Wang, Lina Ren, Jinyuan Yang, Jian Wu, Yongyi Yuan, Pu D |
Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population. Audiology & neuro-otology 2024 1 1-8. Khawla El Fizazi, Meriame Abbassi, Samira Nmer, Hajar Laamarti, Mohamed Noureddine ElAlami, Karim Ouldim, Laila Bouguenouch, Mohammed Rid |
Genetic diagnosis of childhood sensorineural hearing loss. Acta otorrinolaringologica espanola 2024 1 . Sara Reda Del Barrio, Alfredo García Fernández, Juan Francisco Quesada-Espinosa, María Teresa Sánchez-Calvín, Irene Gómez-Manjón, Olalla Sierra-Tomillo, Alexandra Juárez-Rufián, Joaquín de Vergas Gutiérr |
Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China. BMC medical genomics 2024 1 17 (1): 18. Shan Wu, Zhidan Wu, Manlian Chen, Xiangbin Zhong, Haoyan Gu, Wenjing Du, Weidong Liu, Li Lang, Junyi Wa |
- Page last reviewed:Feb 1, 2024
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