Molecules and Cells

Cited by CrossRef (22)

  1. Sara Salime, Majida Charif, Amale Bousfiha, Soukaina Elrharchi, Amina Bakhchane, Hicham Charoute, Mostafa Kabine, Khalid Snoussi, Guy Lenaers, Abdelhamid Barakat. Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families. International Journal of Pediatric Otorhinolaryngology 2017;101:25
    https://doi.org/10.1016/j.ijporl.2017.07.024
  2. Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T. Booth, Hela Azaiez, Devorah Yefet, Adina Quint, Tzvi Weiden, Zippora Brownstein, Michal Macarov, Bella Davidov, John Pappas, Rachel Rabin, Margaret A. Kenna, Andrea M. Oza, Katherine Lafferty, Sami S. Amr, Heidi L. Rehm, Diana L. Kolbe, Kathy Frees, Carla Nishimura, Minjie Luo, Chantal Farra, Cynthia C. Morton, Sholem Y. Scher, Josef Ekstein, Karen B. Avraham, Richard J. H. Smith, Jun Shen. A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing. Eur J Hum Genet 2021;29:988
    https://doi.org/10.1038/s41431-020-00790-w
  3. Bong Jik Kim, Ah Reum Kim, Chung Lee, So Young Kim, Nayoung K. D. Kim, Mun Young Chang, Jihye Rhee, Mi-Hyun Park, Soo Kyung Koo, Min Young Kim, Jin Hee Han, Seung-ha Oh, Woong-Yang Park, Byung Yoon Choi, David Meyre. Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans. PLoS ONE 2016;11:e0165680
    https://doi.org/10.1371/journal.pone.0165680
  4. Mun Young Chang, Chung Lee, Jin Hee Han, Min Young Kim, Hye-Rim Park, Nayoung Kim, Woong-Yang Park, Doo Yi Oh, Byung Yoon Choi. Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness. BMC Med Genet 2018;19
    https://doi.org/10.1186/s12881-018-0541-9
  5. Seung Tae Kim, Kyoung-Mee Kim, Nayoung K.D. Kim, Joon Oh Park, Soomin Ahn, Jae-Won Yun, Kyu-Tae Kim, Se Hoon Park, Peter J. Park, Hee Cheol Kim, Tae Sung Sohn, Dong Il Choi, Jong Ho Cho, Jin Seok Heo, Wooil Kwon, Hyuk Lee, Byung-Hoon Min, Sung No Hong, Young Suk Park, Ho Yeong Lim, Won Ki Kang, Woong-Yang Park, Jeeyun Lee. Clinical Application of Targeted Deep Sequencing in Solid-Cancer Patients and Utility for Biomarker-Selected Clinical Trials. 2017;22:1169
    https://doi.org/10.1634/theoncologist.2017-0020
  6. Luming Wang, Yue Zhang, Qiuxia Xue, Pinghua Huang, Xiaodan Liu. Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non‐syndromic hearing loss . Clinical Laboratory Analysis 2022;36
    https://doi.org/10.1002/jcla.24653
  7. Atteeq U. Rehman, Jonathan E. Bird, Rabia Faridi, Mohsin Shahzad, Sujay Shah, Kwanghyuk Lee, Shaheen N. Khan, Ayesha Imtiaz, Zubair M. Ahmed, Saima Riazuddin, Regie Lyn P. Santos-Cortez, Wasim Ahmad, Suzanne M. Leal, Sheikh Riazuddin, Thomas B. Friedman. Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness. Human Mutation 2016;37:991
    https://doi.org/10.1002/humu.23042
  8. Fengguo Zhang, Lei Xu, Yun Xiao, Jianfeng Li, Xiaohui Bai, Haibo Wang. Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss. Neural Plasticity 2018;2018:1
    https://doi.org/10.1155/2018/5898025
  9. Gina Na, Hye Ji Choi, Sun Young Joo, John Hoon Rim, Jung Ah Kim, Hye-Youn Kim, Seyoung Yu, Yeonsu Jeong, Geun Cheol Shin, Hae Eun Noh, Ho Young Lee, Da Hye Kim, Heon Yung Gee, Jinsei Jung, Jae Young Choi. Heterogeneity of MYO15A variants significantly determine the feasibility of acoustic stimulation with hearing aid and cochlear implant. Hearing Research 2021;404:108227
    https://doi.org/10.1016/j.heares.2021.108227
  10. Mahsa Motavaf, Mahdieh Soveizi, Majid Maleki, Nejat Mahdieh. MYO15A splicing mutations in hearing loss: A review literature and report of a novel mutation. International Journal of Pediatric Otorhinolaryngology 2017;96:35
    https://doi.org/10.1016/j.ijporl.2017.03.008
  11. Sang-Yeon Lee, Jin Hee Han, Bong Jik Kim, Seung Ha Oh, Seungmin Lee, Doo-Yi Oh, Byung Yoon Choi. Identification of a Potential Founder Effect of a Novel PDZD7 Variant Involved in Moderate-to-Severe Sensorineural Hearing Loss in Koreans. IJMS 2019;20:4174
    https://doi.org/10.3390/ijms20174174
  12. Hongbin Zhou, Ahan Kuermanhan, Zhihua Zhang, Wenjing Wang, Jie Dong, Zhou Zhou, Jian Mu, Lin Zhao, Jian Wang, Bing Li, Biaobang Chen. Identification of a novel homozygous mutation in the MYO15A gene in a Kazakh family with non-syndromic hearing loss. International Journal of Pediatric Otorhinolaryngology 2019;125:128
    https://doi.org/10.1016/j.ijporl.2019.06.018
  13. Akram Sarmadi, Samane Nasrniya, Sina Narrei, Zahra Nouri, Hamidreza Abtahi, Mohammad Amin Tabatabaiefar. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss. Mol Biol Rep 2020;47:5355
    https://doi.org/10.1007/s11033-020-05618-w
  14. J-R Chen, Z-H Tang, J Zheng, H-S Shi, J Ding, X-D Qian, C Zhang, J-L Chen, C-C Wang, L Li, J-Z Chen, S-K Yin, J-Z Shao, T-S Huang, P Chen, M-X Guan, J-F Wang. Effects of genetic correction on the differentiation of hair cell-like cells from iPSCs with MYO15A mutation. Cell Death Differ 2016;23:1347
    https://doi.org/10.1038/cdd.2016.16
  15. Wu, Tsai, Lin, Chen, Lin, Cheng, Wu, Lin, Lee, Erdenechuluun, Liu, Chen, Hsu. Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population. Genes 2019;10:772
    https://doi.org/10.3390/genes10100772
  16. Pey-Yu Chen, Cheng-Yu Tsai, Jiunn-Liang Wu, Yi-Lu Li, Che-Ming Wu, Kuang-Chao Chen, Chung-Feng Hwang, Hung-Pin Wu, Hung-Ching Lin, Yen-Fu Cheng, Ming-Yu Lo, Tien-Chen Liu, Ting-Hua Yang, Pei-Lung Chen, Chuan-Jen Hsu, Chen-Chi Wu. Hearing Features and Cochlear Implantation Outcomes in Patients With PathogenicMYO15AVariants: a Multicenter Observational Study. 2022;43:1198
    https://doi.org/10.1097/AUD.0000000000001171
  17. Kyu-Hee Han, Ah Reum Kim, Min Young Kim, Soyeon Ahn, Seung-Ha Oh, Ju Hun Song, Byung Yoon Choi, Dror Sharon. Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans. PLoS ONE 2016;11:e0161756
    https://doi.org/10.1371/journal.pone.0161756
  18. Tohid Ghasemnejad, Mahmoud Shekari Khaniani, Fatemeh Zarei, Mina Farbodnia, Sima Mansoori Derakhshan. An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population. International Journal of Pediatric Otorhinolaryngology 2017;97:113
    https://doi.org/10.1016/j.ijporl.2017.04.007
  19. Shin‐ichi Usami, Shin‐ya Nishio, Hideaki Moteki, Maiko Miyagawa, Hidekane Yoshimura. Cochlear Implantation From the Perspective of Genetic Background. Anat. Rec. 2020;303:563
    https://doi.org/10.1002/ar.24360
  20. Jin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jin-Cao Xu, Ying Fu, Dong-Yang Kang, Kun Yang, Xin Zhang, Xing Liu, Xue Gao, Yong-Yi Yuan, Pu Dai. Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A. BMC Med Genomics 2022;15
    https://doi.org/10.1186/s12920-022-01368-9
  21. Athar Khalil, Samer Bou Karroum, Rana Barake, Gabriel Dunya, Samer Abou-Rizk, Amina Kamar, Georges Nemer, Marc Bassim. Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF. BMC Med Genet 2020;21
    https://doi.org/10.1186/s12881-019-0942-4
  22. Jing Zhang, Jing Guan, Hongyang Wang, Linwei Yin, Dayong Wang, Lidong Zhao, Huifang Zhou, Qiuju Wang. Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss. BMC Med Genet 2019;20
    https://doi.org/10.1186/s12881-019-0790-2