Literature DB >> 1952587

Genetic epidemiology of hearing impairment.

N E Morton1.   

Abstract

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Year:  1991        PMID： 1952587     DOI： 10.1111/j.1749-6632.1991.tb19572.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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  228 in total

1.  Inherited deafness in childhood--the genetic revolution unmasks the clinical challenge.

Authors:  W Reardon; R F Mueller
Journal:  Arch Dis Child       Date:  2000-04       Impact factor: 3.791

2.  DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

Authors:  C C Greene; P M McMillan; S E Barker; P Kurnool; M I Lomax; M Burmeister; M M Lesperance
Journal:  Am J Hum Genet       Date:  2000-12-11       Impact factor: 11.025

3.  A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.

Authors:  Asli Sirmaci; Seyra Erbek; Justin Price; Mingqian Huang; Duygu Duman; F Başak Cengiz; Güney Bademci; Suna Tokgöz-Yilmaz; Burcu Hişmi; Hilal Ozdağ; Banu Oztürk; Sevsen Kulaksizoğlu; Erkan Yildirim; Haris Kokotas; Maria Grigoriadou; Michael B Petersen; Hashem Shahin; Moien Kanaan; Mary-Claire King; Zheng-Yi Chen; Susan H Blanton; Xue Z Liu; Stephan Zuchner; Nejat Akar; Mustafa Tekin
Journal:  Am J Hum Genet       Date:  2010-05-06       Impact factor: 11.025

4.  Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

Authors:  J M Bork; L M Peters; S Riazuddin; S L Bernstein; Z M Ahmed; S L Ness; R Polomeno; A Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Z Ahmed; S N Khan; V M Kaloustian; X C Li; A Lalwani; S Riazuddin; M Bitner-Glindzicz; W E Nance; X Z Liu; G Wistow; R J Smith; A J Griffith; E R Wilcox; T B Friedman; R J Morell
Journal:  Am J Hum Genet       Date:  2000-11-21       Impact factor: 11.025

Review 5.  Genetics of hearing loss: where are we standing now?

Authors:  Hossein Mahboubi; Sami Dwabe; Matthew Fradkin; Virginia Kimonis; Hamid R Djalilian
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-01-05       Impact factor: 2.503

6.  Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.

Authors:  A Eliot Shearer; Adam P DeLuca; Michael S Hildebrand; Kyle R Taylor; José Gurrola; Steve Scherer; Todd E Scheetz; Richard J H Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-15       Impact factor: 11.205

7.  Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.

Authors:  Hui Zhao; Ronghua Li; Qiuju Wang; Qingfeng Yan; Jian-Hong Deng; Dongyi Han; Yidong Bai; Wie-Yen Young; Min-Xin Guan
Journal:  Am J Hum Genet       Date:  2003-12-12       Impact factor: 11.025

8.  The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23.

Authors:  G Ali; R L P Santos; P John; M A L Wambangco; K Lee; W Ahmad; Sm Leal
Journal:  Clin Genet       Date:  2006-05       Impact factor: 4.438

9.  A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness.

Authors:  John Patton; Carmen Brewer; Wade Chien; Jennifer J Johnston; Andrew J Griffith; Leslie G Biesecker
Journal:  Eur J Hum Genet       Date:  2016-10-19       Impact factor: 4.246

10.  [Phenotype of patients showing hearing impairment based on the 35delG mutation in the connexin 26 gene].

Authors:  T Tóth; S Kupka; I Sziklai; N Blin; H-P Zenner; M Pfister
Journal:  HNO       Date:  2003-03-27       Impact factor: 1.284
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