Literature DB >> 23280582

AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screening.

Kyle R Taylor1, Adam P Deluca, A Eliot Shearer, Michael S Hildebrand, E Ann Black-Ziegelbein, V Nikhil Anand, Christina M Sloan, Robert W Eppsteiner, Todd E Scheetz, Patrick L M Huygen, Richard J H Smith, Terry A Braun, Thomas L Casavant.   

Abstract

Autosomal dominant nonsyndromic hearing loss (ADNSHL) is a common and often progressive sensory deficit. ADNSHL displays a high degree of genetic heterogeneity and varying rates of progression. Accurate, comprehensive, and cost-effective genetic testing facilitates genetic counseling and provides valuable prognostic information to affected individuals. In this article, we describe the algorithm underlying AudioGene, a software system employing machine-learning techniques that utilizes phenotypic information derived from audiograms to predict the genetic cause of hearing loss in persons segregating ADNSHL. Our data show that AudioGene has an accuracy of 68% in predicting the causative gene within its top three predictions, as compared with 44% for a majority classifier. We also show that AudioGene remains effective for audiograms with high levels of clinical measurement noise. We identify audiometric outliers for each genetic locus and hypothesize that outliers may reflect modifying genetic effects. As personalized genomic medicine becomes more common, AudioGene will be increasingly useful as a phenotypic filter to assess pathogenicity of variants identified by massively parallel sequencing.
© 2012 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23280582      PMCID: PMC3753227          DOI: 10.1002/humu.22268

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  16 in total

Review 1.  The current status of EHDI programs in the United States.

Authors:  Karl R White
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2003

Review 2.  Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

Authors:  Nele Hilgert; Richard J H Smith; Guy Van Camp
Journal:  Mutat Res       Date:  2008-08-29       Impact factor: 2.433

3.  The societal costs of severe to profound hearing loss in the United States.

Authors:  P E Mohr; J J Feldman; J L Dunbar; A McConkey-Robbins; J K Niparko; R K Rittenhouse; M W Skinner
Journal:  Int J Technol Assess Health Care       Date:  2000       Impact factor: 2.188

4.  Using the phenome and genome to improve genetic diagnosis for deafness.

Authors:  Robert W Eppsteiner; A Eliot Shearer; Michael S Hildebrand; Kyle R Taylor; Adam P Deluca; Steve Scherer; Patrick Huygen; Todd E Scheetz; Terry A Braun; Thomas L Casavant; Richard J H Smith
Journal:  Otolaryngol Head Neck Surg       Date:  2012-07-11       Impact factor: 3.497

5.  GJB2 mutations and degree of hearing loss: a multicenter study.

Authors:  Rikkert L Snoeckx; Patrick L M Huygen; Delphine Feldmann; Sandrine Marlin; Françoise Denoyelle; Jaroslaw Waligora; Malgorzata Mueller-Malesinska; Agneszka Pollak; Rafal Ploski; Alessandra Murgia; Eva Orzan; Pierangela Castorina; Umberto Ambrosetti; Ewa Nowakowska-Szyrwinska; Jerzy Bal; Wojciech Wiszniewski; Andreas R Janecke; Doris Nekahm-Heis; Pavel Seeman; Olga Bendova; Margaret A Kenna; Anna Frangulov; Heidi L Rehm; Mustafa Tekin; Armagan Incesulu; Hans-Henrik M Dahl; Desirée du Sart; Lucy Jenkins; Deirdre Lucas; Maria Bitner-Glindzicz; Karen B Avraham; Zippora Brownstein; Ignacio del Castillo; Felipe Moreno; Nikolaus Blin; Markus Pfister; Istvan Sziklai; Timea Toth; Philip M Kelley; Edward S Cohn; Lionel Van Maldergem; Pascale Hilbert; Anne-Françoise Roux; Michel Mondain; Lies H Hoefsloot; Cor W R J Cremers; Tuija Löppönen; Heikki Löppönen; Agnete Parving; Karen Gronskov; Iris Schrijver; Joseph Roberson; Francesca Gualandi; Alessandro Martini; Geneviéve Lina-Granade; Nathalie Pallares-Ruiz; Céu Correia; Graça Fialho; Kim Cryns; Nele Hilgert; Paul Van de Heyning; Carla J Nishimura; Richard J H Smith; Guy Van Camp
Journal:  Am J Hum Genet       Date:  2005-10-19       Impact factor: 11.025

Review 6.  Sensorineural hearing loss in children.

Authors:  Richard J H Smith; James F Bale; Karl R White
Journal:  Lancet       Date:  2005 Mar 5-11       Impact factor: 79.321

7.  Data mining in bioinformatics using Weka.

Authors:  Eibe Frank; Mark Hall; Len Trigg; Geoffrey Holmes; Ian H Witten
Journal:  Bioinformatics       Date:  2004-04-08       Impact factor: 6.937

8.  Test-retest reliability of pure-tone thresholds from 0.5 to 16 kHz using Sennheiser HDA 200 and Etymotic Research ER-2 earphones.

Authors:  Nicolas Schmuziger; Rudolf Probst; Jacek Smurzynski
Journal:  Ear Hear       Date:  2004-04       Impact factor: 3.570

Review 9.  Early hearing detection and intervention programs: opportunities for genetic services.

Authors:  Karl R White
Journal:  Am J Med Genet A       Date:  2004-09-15       Impact factor: 2.802

10.  Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus.

Authors:  Michael S Hildebrand; Dylan Tack; Sarah J McMordie; Adam DeLuca; In Ae Hur; Carla Nishimura; Patrick Huygen; Thomas L Casavant; Richard J H Smith
Journal:  Genet Med       Date:  2008-11       Impact factor: 8.822

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  15 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

Review 2.  Congenital hearing loss.

Authors:  Anna M H Korver; Richard J H Smith; Guy Van Camp; Mark R Schleiss; Maria A K Bitner-Glindzicz; Lawrence R Lustig; Shin-Ichi Usami; An N Boudewyns
Journal:  Nat Rev Dis Primers       Date:  2017-01-12       Impact factor: 52.329

3.  A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.

Authors:  W Daniel Walls; Hideaki Moteki; Taylor R Thomas; Shin-Ya Nishio; Hidekane Yoshimura; Yoichiro Iwasa; Kathy L Frees; Carla J Nishimura; Hela Azaiez; Kevin T Booth; Robert J Marini; Diana L Kolbe; A Monique Weaver; Amanda M Schaefer; Kai Wang; Terry A Braun; Shin-Ichi Usami; Peter G Barr-Gillespie; Guy P Richardson; Richard J Smith; Thomas L Casavant
Journal:  Hum Genet       Date:  2020-05-07       Impact factor: 4.132

Review 4.  [Personalized medicine in otology. The role of genetic diagnostics in patients with hearing impairment].

Authors:  N Friese; K Braun; M Müller; A Tropitzsch
Journal:  HNO       Date:  2015-06       Impact factor: 1.284

5.  The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study.

Authors:  Ryan K Thorpe; Hela Azaiez; Peina Wu; Qiuju Wang; Lei Xu; Pu Dai; Tao Yang; G Bradley Schaefer; B Robert Peters; Kenny H Chan; Krista S Schatz; Joann Bodurtha; Nathaniel H Robin; Yoel Hirsch; Zuhair Abdalla Rahbeeni; Huijun Yuan; Richard J H Smith
Journal:  Hum Genet       Date:  2021-08-23       Impact factor: 5.881

6.  AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss.

Authors:  Ryan K Thorpe; W Daniel Walls; Rae Corrigan; Amanda Schaefer; Kai Wang; Patrick Huygen; Thomas L Casavant; Richard J H Smith
Journal:  Hum Genet       Date:  2022-01-17       Impact factor: 5.881

7.  Audioprofile Surfaces: The 21st Century Audiogram.

Authors:  Kyle R Taylor; Kevin T Booth; Hela Azaiez; Christina M Sloan; Diana L Kolbe; Emily N Glanz; A Eliot Shearer; Adam P DeLuca; V Nikhil Anand; Michael S Hildebrand; Allen C Simpson; Robert W Eppsteiner; Todd E Scheetz; Terry A Braun; Patrick L M Huygen; Richard J H Smith; Thomas L Casavant
Journal:  Ann Otol Rhinol Laryngol       Date:  2015-11-03       Impact factor: 1.547

8.  Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss.

Authors:  Marjan Masoudi; Najmeh Ahangari; Ali Akbar Poursadegh Zonouzi; Ahmad Poursadegh Zonouzi; Azim Nejatizadeh
Journal:  Iran J Public Health       Date:  2016-05       Impact factor: 1.429

9.  Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss.

Authors:  Justin A Pater; Jane Green; Darren D O'Rielly; Anne Griffin; Jessica Squires; Taylor Burt; Sara Fernandez; Bridget Fernandez; Jim Houston; Jiayi Zhou; Nicole M Roslin; Terry-Lynn Young
Journal:  BMC Med Genet       Date:  2019-05-02       Impact factor: 2.103

Review 10.  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

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