Literature DB >> 27552069

Navigating genetic diagnostics in patients with hearing loss.

Christina M Sloan-Heggen1, Richard J H Smith.   

Abstract

PURPOSE OF REVIEW: In the age of targeted genomic enrichment and massively parallel sequencing, there is no more efficient genetic testing method for the diagnosis of hereditary hearing loss. More clinical tests are on the market, which can make choosing good tests difficult. RECENT
FINDINGS: More and larger comprehensive genetic studies in patients with hearing loss have been published recently. They remind us of the importance of looking for both single nucleotide variation and copy number variation in all genes implicated in nonsyndromic hearing loss. They also inform us of how a patient's history and phenotype provide essential information in the interpretation of genetic data.
SUMMARY: Choosing the most comprehensive genetic test improves the chances of a genetic diagnosis and thereby impacts clinical care.

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Year:  2016        PMID: 27552069      PMCID: PMC5241053          DOI: 10.1097/MOP.0000000000000410

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  56 in total

1.  CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.

Authors:  Lennart F Johansson; Freerk van Dijk; Eddy N de Boer; Krista K van Dijk-Bos; Jan D H Jongbloed; Annemieke H van der Hout; Helga Westers; Richard J Sinke; Morris A Swertz; Rolf H Sijmons; Birgit Sikkema-Raddatz
Journal:  Hum Mutat       Date:  2016-02-24       Impact factor: 4.878

2.  The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.

Authors:  Maiko Miyagawa; Shin-Ya Nishio; Yuika Sakurai; Mitsuru Hattori; Keita Tsukada; Hideaki Moteki; Hiromi Kojima; Shin-Ichi Usami
Journal:  Ann Otol Rhinol Laryngol       Date:  2015-03-13       Impact factor: 1.547

3.  Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families.

Authors:  K Lebeko; C M Sloan-Heggen; J J N Noubiap; C Dandara; D L Kolbe; S S Ephraim; K T Booth; H Azaiez; R L P Santos-Cortez; S M Leal; R J H Smith; A Wonkam
Journal:  Clin Genet       Date:  2016-06-01       Impact factor: 4.438

Review 4.  Whole-exome sequencing and its impact in hereditary hearing loss.

Authors:  Tahir Atik; Guney Bademci; Oscar Diaz-Horta; Susan H Blanton; Mustafa Tekin
Journal:  Genet Res (Camb)       Date:  2015-03-31       Impact factor: 1.588

5.  Detailed hearing and vestibular profiles in the patients with COCH mutations.

Authors:  Keita Tsukada; Aya Ichinose; Maiko Miyagawa; Kentaro Mori; Mitsuru Hattori; Shin-Ya Nishio; Yasushi Naito; Shin-Ichiro Kitajiri; Shin-Ichi Usami
Journal:  Ann Otol Rhinol Laryngol       Date:  2015-03-16       Impact factor: 1.547

6.  Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in Japan.

Authors:  Shin-Ya Nishio; Shin-Ichi Usami
Journal:  Ann Otol Rhinol Laryngol       Date:  2015-03-18       Impact factor: 1.547

7.  Whole USH2A Gene Sequencing Identifies Several New Deep Intronic Mutations.

Authors:  Alessandro Liquori; Christel Vaché; David Baux; Catherine Blanchet; Christian Hamel; Sue Malcolm; Michel Koenig; Mireille Claustres; Anne-Françoise Roux
Journal:  Hum Mutat       Date:  2015-11-23       Impact factor: 4.878

8.  Using ClinVar as a Resource to Support Variant Interpretation.

Authors:  Steven M Harrison; Erin R Riggs; Donna R Maglott; Jennifer M Lee; Danielle R Azzariti; Annie Niehaus; Erin M Ramos; Christa L Martin; Melissa J Landrum; Heidi L Rehm
Journal:  Curr Protoc Hum Genet       Date:  2016-04-01

9.  Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.

Authors:  Christina M Sloan-Heggen; Mojgan Babanejad; Maryam Beheshtian; Allen C Simpson; Kevin T Booth; Fariba Ardalani; Kathy L Frees; Marzieh Mohseni; Reza Mozafari; Zohreh Mehrjoo; Leila Jamali; Saeideh Vaziri; Tara Akhtarkhavari; Niloofar Bazazzadegan; Nooshin Nikzat; Sanaz Arzhangi; Farahnaz Sabbagh; Hasan Otukesh; Seyed Morteza Seifati; Hossein Khodaei; Maryam Taghdiri; Nicole C Meyer; Ahmad Daneshi; Mohammad Farhadi; Kimia Kahrizi; Richard J H Smith; Hela Azaiez; Hossein Najmabadi
Journal:  J Med Genet       Date:  2015-10-07       Impact factor: 6.318

10.  American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss.

Authors:  Raye L Alford; Kathleen S Arnos; Michelle Fox; Jerry W Lin; Christina G Palmer; Arti Pandya; Heidi L Rehm; Nathaniel H Robin; Daryl A Scott; Christine Yoshinaga-Itano
Journal:  Genet Med       Date:  2014-03-20       Impact factor: 8.822

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  10 in total

Review 1.  Outlook and future of inner ear therapy.

Authors:  Jenna Devare; Samuel Gubbels; Yehoash Raphael
Journal:  Hear Res       Date:  2018-05-17       Impact factor: 3.208

2.  Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.

Authors:  Jie Wu; Zongfu Cao; Yu Su; Yang Wang; Ruikun Cai; Jiyue Chen; Bo Gao; Mingyu Han; Xiaohong Li; DeJun Zhang; Xue Gao; Shasha Huang; Quanfei Huang; Yongyi Yuan; Xu Ma; Pu Dai
Journal:  J Hum Genet       Date:  2022-08-19       Impact factor: 3.755

3.  Target-Sequencing of Female Infertility Pathogenic Gene Panel and a Novel TUBB8 Loss-of-Function Mutation.

Authors:  Hongxia Yuan; Jianhua Chen; Na Li; Hui Miao; Yao Chen; Shuyan Lyu; Yu Qiao; Guangping Yang; Hui Luo; Liangliang Chen; Fei Mao; Lingli Huang; Yanni He; Saifei Hu; Congxiu Miao; Yun Qian; Ruizhi Feng
Journal:  Front Genet       Date:  2022-05-10       Impact factor: 4.772

4.  ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.

Authors:  Alex M Rohacek; Thomas W Bebee; Richard K Tilton; Caleb M Radens; Chris McDermott-Roe; Natoya Peart; Maninder Kaur; Michael Zaykaner; Benjamin Cieply; Kiran Musunuru; Yoseph Barash; John A Germiller; Ian D Krantz; Russ P Carstens; Douglas J Epstein
Journal:  Dev Cell       Date:  2017-10-26       Impact factor: 12.270

5.  Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.

Authors:  Elodie M Richard; Regie Lyn P Santos-Cortez; Rabia Faridi; Atteeq U Rehman; Kwanghyuk Lee; Mohsin Shahzad; Anushree Acharya; Asma A Khan; Ayesha Imtiaz; Imen Chakchouk; Christina Takla; Izoduwa Abbe; Maria Rafeeq; Khurram Liaqat; Taimur Chaudhry; Michael J Bamshad; Deborah A Nickerson; Isabelle Schrauwen; Shaheen N Khan; Robert J Morell; Saba Zafar; Muhammad Ansar; Zubair M Ahmed; Wasim Ahmad; Sheikh Riazuddin; Thomas B Friedman; Suzanne M Leal; Saima Riazuddin
Journal:  Hum Mutat       Date:  2018-11-18       Impact factor: 4.878

6.  The Genetic contribution to solving the cocktail-party problem.

Authors:  Samuel R Mathias; Emma E M Knowles; Josephine Mollon; Amanda L Rodrigue; Mary K Woolsey; Alyssa M Hernandez; Amy S Garrett; Peter T Fox; Rene L Olvera; Juan M Peralta; Satish Kumar; Harald H H Göring; Ravi Duggirala; Joanne E Curran; John Blangero; David C Glahn
Journal:  iScience       Date:  2022-08-24

7.  Outcomes of Gene Panel Testing for Sensorineural Hearing Loss in a Diverse Patient Cohort.

Authors:  Elizabeth N Liao; Emily Taketa; Noura I Mohamad; Dylan K Chan
Journal:  JAMA Netw Open       Date:  2022-09-01

8.  Hereditary hearing loss SNP-microarray pilot study.

Authors:  Barbara Vona; Michaela A H Hofrichter; Jörg Schröder; Wafaa Shehata-Dieler; Indrajit Nanda; Thomas Haaf
Journal:  BMC Res Notes       Date:  2018-06-14

Review 9.  Diagnosing and Preventing Hearing Loss in the Genomic Age.

Authors:  John H McDermott; Leslie P Molina-Ramírez; Iain A Bruce; Ajit Mahaveer; Mark Turner; Gino Miele; Richard Body; Rachel Mahood; Fiona Ulph; Rhona MacLeod; Karen Harvey; Nicola Booth; Leigh A M Demain; Paul Wilson; Graeme C Black; Cynthia C Morton; William G Newman
Journal:  Trends Hear       Date:  2019 Jan-Dec       Impact factor: 3.293

10.  Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene.

Authors:  Paola Tesolin; Anna Morgan; Michela Notarangelo; Rocco Pio Ortore; Maria Pina Concas; Angelantonio Notarangelo; Giorgia Girotto
Journal:  Genes (Basel)       Date:  2021-07-06       Impact factor: 4.096

  10 in total

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