Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: TECTA[original query] |
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Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations. Journal of human genetics 2010 Oct 55 (10): 639-48. Mahdieh Nejat, Rabbani Bahareh, Wiley Susan, Akbari Mohammad Taghi, Zeinali Siro |
Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss. Annals of clinical and laboratory science 2010 40 (4): 380-5. Sagong Borum, Park Raekil, Kim Yee Hyuk, Lee Kyu-Yup, Baek Jeong-In, Cho Hyun-Joo, Cho In-Jee, Kim Un-Kyung, Lee Sang-He |
Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss. Genetic testing and molecular biomarkers 2016 Sep . Chen Siqi, Dong Cheng, Wang Qi, Zhong Zhen, Qi Yu, Ke Xiaomei, Liu Yu |
Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss. Orphanet journal of rare diseases 2017 9 12 (1): 157. Yamamoto Nobuko, Mutai Hideki, Namba Kazunori, Morita Noriko, Masuda Shin, Nishi Yasuyuki, Nakano Atsuko, Masuda Sawako, Fujioka Masato, Kaga Kimitaka, Ogawa Kaoru, Matsunaga Tats |
Novel West syndrome candidate genes in a Chinese cohort. CNS neuroscience & therapeutics 2018 4 24 (12): 1196-1206. Peng Jing, Wang Ying, He Fang, Chen Chen, Wu Li-Wen, Yang Li-Fen, Ma Yu-Ping, Zhang Wen, Shi Zi-Qing, Chen Chao, Xia Kun, Guo Hui, Yin Fei, Pang N |
Independent replication of polymorphisms predicting toxicity in breast cancer patients randomized between dose-dense and docetaxel-containing adjuvant chemotherapy. Oncotarget 2017 Dec 8 (69): 113531-113542. van Rossum Annelot G J, Kok Marleen, McCool Danielle, Opdam Mark, Miltenburg Nienke C, Mandjes Ingrid A M, van Leeuwen-Stok Elise, Imholz Alex L T, Portielje Johanneke E A, Bos Monique M E M, van Bochove Aart, van Werkhoven Erik, Schmidt Marjanka K, Oosterkamp Hendrika M, Linn Sabine |
The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss. Genes 2019 9 10 (10): . Yasukawa Rika, Moteki Hideaki, Nishio Shin-Ya, Ishikawa Kotaro, Abe Satoko, Honkura Yohei, Hyogo Misako, Mihashi Ryota, Ikezono Tetsuo, Shintani Tomoko, Ogasawara Noriko, Shirai Kyoko, Yoshihashi Hiroshi, Ishino Takashi, Otsuki Koshi, Ito Tsukasa, Sugahara Kazuma, Usami Shin-Ic |
Systematic Review of Hearing Loss Genes in the African American Population. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2019 5 40 (5): e488-e496. Worden Cameron P, Jeyakumar Ani |
The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report. BMC medical genetics 2019 4 20 (1): 57. Nam Gi-Sung, Rim John Hoon, Choi Jae Young, Gee Heon Yung, Choi Jong Rak, Lee Seung-Tae, Jung Jins |
[Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 2 36 (2): 147-150. Zhou Chiyan, Li Suping, Song Qinhao, Liu Xiaodan, Miao Zhengy |
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations. Frontiers in genetics 2019 1 9 681. Morgan Anna, Lenarduzzi Stefania, Cappellani Stefania, Pecile Vanna, Morgutti Marcello, Orzan Eva, Ghiselli Sara, Ambrosetti Umberto, Brumat Marco, Gajendrarao Poornima, La Bianca Martina, Faletra Flavio, Grosso Enrico, Sirchia Fabio, Sensi Alberto, Graziano Claudio, Seri Marco, Gasparini Paolo, Girotto Giorg |
A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Human genetics 2020 5 139 (10): 1315-1323. Walls W Daniel, Moteki Hideaki, Thomas Taylor R, Nishio Shin-Ya, Yoshimura Hidekane, Iwasa Yoichiro, Frees Kathy L, Nishimura Carla J, Azaiez Hela, Booth Kevin T, Marini Robert J, Kolbe Diana L, Weaver A Monique, Schaefer Amanda M, Wang Kai, Braun Terry A, Usami Shin-Ichi, Barr-Gillespie Peter G, Richardson Guy P, Smith Richard J, Casavant Thomas |
Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families. Neural plasticity 2021 5 2021 5528434. Mei Xueshuang, Zhou Yaqi, Amjad Muhammad, Yang Weiqiang, Zhu Rufei, Asif Muhammad, Hussain Hafiz Muhammad Jafar, Yang Tao, Iqbal Furhan, Hu Hong |
Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss. Scientific reports 2021 11 11 (1): 22488. Pavlenkova Zuzana, Varga Lukas, Borecka Silvia, Karhanek Miloslav, Huckova Miloslava, Skopkova Martina, Profant Milan, Gasperikova Danie |
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.
Communications biology 2021 Oct 4 (1): 1148. Skuladottir Astros Th, Bjornsdottir Gyda, Nawaz Muhammad Sulaman, Petersen Hannes, Rognvaldsson Solvi, Moore Kristjan Helgi Swerford, Olafsson Pall I, Magnusson Sigurður H, Bjornsdottir Anna, Sveinsson Olafur A, Sigurdardottir Gudrun R, Saevarsdottir Saedis, Ivarsdottir Erna V, Stefansdottir Lilja, Gunnarsson Bjarni, Muhlestein Joseph B, Knowlton Kirk U, Jones David A, Nadauld Lincoln D, Hartmann Annette M, Rujescu Dan, Strupp Michael, Walters G Bragi, Thorgeirsson Thorgeir E, Jonsdottir Ingileif, Holm Hilma, Thorleifsson Gudmar, Gudbjartsson Daniel F, Sulem Patrick, Stefansson Hreinn, Stefansson Ka |
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study. Cytogenetic and genome research 2022 5 162 (1-2): 1-9. Reis Cláudia Sousa, Quental Sofia, Fernandes Susana, Castedo Sérgio, Moura Carla Pin |
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility. Acta neuropathologica 2022 5 144 (1): 107-127. Silvennoinen Katri, Gawel Kinga, Tsortouktzidis Despina, Pitsch Julika, Alhusaini Saud, van Loo Karen M J, Picardo Richard, Michalak Zuzanna, Pagni Susanna, Martins Custodio Helena, Mills James, Whelan Christopher D, de Zubicaray Greig I, McMahon Katie L, van der Ent Wietske, Kirstein-Smardzewska Karolina J, Tiraboschi Ettore, Mudge Jonathan M, Frankish Adam, Thom Maria, Wright Margaret J, Thompson Paul M, Schoch Susanne, Becker Albert J, Esguerra Camila V, Sisodiya Sanjay |
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 |
Rare-variant association analysis reveals known and new age-related hearing loss genes. European journal of human genetics : EJHG 2023 2 . Cornejo-Sanchez Diana M, Li Guangyou, Fabiha Tabassum, Wang Ran, Acharya Anushree, Everard Jenna L, Kadlubowska Magda K, Huang Yin, Schrauwen Isabelle, Wang Gao T, DeWan Andrew T, Leal Suzanne |
Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report. Croatian medical journal 2023 11 64 (5): 329-333. Ivona Sansovi?, Ana-Maria Meaši?, Ljubica Odak, Mijana Ke |
MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population. BMC medical genomics 2024 1 17 (1): 32. Lang Zhang, Jin-Yuan Yang, Qiu-Quan Wang, Xue Gao, Guo-Jian Wang, Ming-Yu Han, Dong-Yang Kang, Dong-Yi Han, Sha-Sha Huang, Yong-Yi Yu |
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- Page last updated:Apr 16, 2024
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