Literature DB >> 33111345

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.

Zippora Brownstein1, Suleyman Gulsuner2, Tom Walsh2, Fábio T A Martins1, Shahar Taiber1, Ofer Isakov3, Ming K Lee2, Mor Bordeynik-Cohen1, Maria Birkan1,4, Weise Chang5, Silvia Casadei2, Nada Danial-Farran1,6,7, Amal Abu-Rayyan1,8, Ryan Carlson2, Lara Kamal8, Asgeir Ö Arnthórsson9, Meirav Sokolov1,10, Dror Gilony1,10, Noga Lipschitz1,11, Moshe Frydman1,12, Bella Davidov4, Michal Macarov13, Michal Sagi13, Chana Vinkler14, Hana Poran12, Reuven Sharony15, Nadra Samra16, Na'ama Zvi13, Hagit Baris-Feldman17, Amihood Singer18, Ophir Handzel19, Ronna Hertzano20, Doaa Ali-Naffaa1,21, Noa Ruhrman-Shahar4, Ory Madgar11, Efrat Sofrin-Drucker4, Amir Peleg21, Morad Khayat6, Mordechai Shohat1,22,23, Lina Basel-Salmon1,4, Elon Pras1,12, Dorit Lev1,14, Michael Wolf11, Eirikur Steingrimsson9, Noam Shomron3, Matthew W Kelley5, Moien N Kanaan8, Stavit Allon-Shalev6,7, Mary-Claire King2, Karen B Avraham1.   

Abstract

Mutations in more than 150 genes are responsible for inherited hearing loss, with thousands of different, severe causal alleles that vary among populations. The Israeli Jewish population includes communities of diverse geographic origins, revealing a wide range of deafness-associated variants and enabling clinical characterization of the associated phenotypes. Our goal was to identify the genetic causes of inherited hearing loss in this population, and to determine relationships among genotype, phenotype, and ethnicity. Genomic DNA samples from informative relatives of 88 multiplex families, all of self-identified Jewish ancestry, with either non-syndromic or syndromic hearing loss, were sequenced for known and candidate deafness genes using the HEar-Seq gene panel. The genetic causes of hearing loss were identified for 60% of the families. One gene was encountered for the first time in human hearing loss: ATOH1 (Atonal), a basic helix-loop-helix transcription factor responsible for autosomal dominant progressive hearing loss in a five-generation family. Our results show that genomic sequencing with a gene panel dedicated to hearing loss is effective for genetic diagnoses in a diverse population. Comprehensive sequencing enables well-informed genetic counseling and clinical management by medical geneticists, otolaryngologists, audiologists, and speech therapists and can be integrated into newborn screening for deafness.
© 2020 John Wiley & Sons A/S . Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  deafness; diagnostics; gene panel; genomics; hearing; massively parallel sequencing; next‐generation sequencing

Mesh:

Substances:

Year:  2020        PMID: 33111345      PMCID: PMC8045518          DOI: 10.1111/cge.13817

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.296


  55 in total

1.  GATA3 abnormalities and the phenotypic spectrum of HDR syndrome.

Authors:  K Muroya; T Hasegawa; Y Ito; T Nagai; H Isotani; Y Iwata; K Yamamoto; S Fujimoto; S Seishu; Y Fukushima; Y Hasegawa; T Ogata
Journal:  J Med Genet       Date:  2001-06       Impact factor: 6.318

2.  The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestry.

Authors:  Doron M Behar; Bella Davidov; Zippora Brownstein; Tamar Ben-Yosef; Karen B Avraham; Mordechai Shohat
Journal:  Genet Test Mol Biomarkers       Date:  2013-12-24

3.  De novo SOX10 nonsense mutation in a patient with Kallmann syndrome and hearing loss.

Authors:  Kirsi Vaaralahti; Johanna Tommiska; Vallo Tillmann; Natalja Liivak; Johanna Känsäkoski; Eeva-Maria Laitinen; Taneli Raivio
Journal:  Pediatr Res       Date:  2014-04-25       Impact factor: 3.756

4.  Biological Therapies of the Inner Ear: What Otologists Need to Consider.

Authors:  Anne G M Schilder; Helen Blackshaw; Thomas Lenarz; Athanasia Warnecke; Lawrence R Lustig; Hinrich Staecker
Journal:  Otol Neurotol       Date:  2018-02       Impact factor: 2.311

5.  The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.

Authors:  T Sobe; S Vreugde; H Shahin; M Berlin; N Davis; M Kanaan; Y Yaron; A Orr-Urtreger; M Frydman; M Shohat; K B Avraham
Journal:  Hum Genet       Date:  2000-01       Impact factor: 4.132

6.  The role of Math1 in inner ear development: Uncoupling the establishment of the sensory primordium from hair cell fate determination.

Authors:  Ping Chen; Jane E Johnson; Huda Y Zoghbi; Neil Segil
Journal:  Development       Date:  2002-05       Impact factor: 6.868

7.  Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing.

Authors:  Mark B Consugar; Daniel Navarro-Gomez; Emily M Place; Kinga M Bujakowska; Maria E Sousa; Zoë D Fonseca-Kelly; Daniel G Taub; Maria Janessian; Dan Yi Wang; Elizabeth D Au; Katherine B Sims; David A Sweetser; Anne B Fulton; Qin Liu; Janey L Wiggs; Xiaowu Gai; Eric A Pierce
Journal:  Genet Med       Date:  2014-11-20       Impact factor: 8.822

8.  Genetics and genomic medicine in Israel.

Authors:  Joël Zlotogora
Journal:  Mol Genet Genomic Med       Date:  2014-03       Impact factor: 2.183

9.  Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.

Authors:  Nobuko Yamamoto; Hideki Mutai; Kazunori Namba; Noriko Morita; Shin Masuda; Yasuyuki Nishi; Atsuko Nakano; Sawako Masuda; Masato Fujioka; Kimitaka Kaga; Kaoru Ogawa; Tatsuo Matsunaga
Journal:  Orphanet J Rare Dis       Date:  2017-09-25       Impact factor: 4.123

Review 10.  Genetic Therapies for Hearing Loss: Accomplishments and Remaining Challenges.

Authors:  Shahar Taiber; Karen B Avraham
Journal:  Neurosci Lett       Date:  2019-10-03       Impact factor: 3.046

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  6 in total

Review 1.  The noncoding genome and hearing loss.

Authors:  Karen B Avraham; Lama Khalaily; Yael Noy; Lara Kamal; Tal Koffler-Brill; Shahar Taiber
Journal:  Hum Genet       Date:  2021-09-07       Impact factor: 4.132

2.  Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss.

Authors:  Shin-Ya Nishio; Shin-Ichi Usami
Journal:  Hum Genet       Date:  2021-09-14       Impact factor: 5.881

3.  Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness.

Authors:  Shahar Taiber; Roie Cohen; Ofer Yizhar-Barnea; David Sprinzak; Jeffrey R Holt; Karen B Avraham
Journal:  EMBO Mol Med       Date:  2020-12-22       Impact factor: 12.137

Review 4.  The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.

Authors:  Shin-Ichi Usami; Shin-Ya Nishio
Journal:  Hum Genet       Date:  2021-10-01       Impact factor: 5.881

5.  Biallelic ATOH1 Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing Loss.

Authors:  Tanja Višnjar; Aleš Maver; Karin Writzl; Ornela Maloku; Gaber Bergant; Helena Jaklič; David Neubauer; Federico Fogolari; Nuška Pečarič Meglič; Borut Peterlin
Journal:  Neurol Genet       Date:  2022-05-03

6.  Molecular Features of SLC26A4 Common Variant p.L117F.

Authors:  Arnoldas Matulevičius; Emanuele Bernardinelli; Zippora Brownstein; Sebastian Roesch; Karen B Avraham; Silvia Dossena
Journal:  J Clin Med       Date:  2022-09-22       Impact factor: 4.964

  6 in total

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