Literature DB >> 12746422

Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.

M RamShankar1, S Girirajan, O Dagan, H M Ravi Shankar, R Jalvi, R Rangasayee, K B Avraham, A Anand.   

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Year:  2003        PMID： 12746422      PMCID： PMC1735461          DOI： 10.1136/jmg.40.5.e68

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  45 in total

1.  Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia.

Authors:  L U Dzhemileva; O L Posukh; N A Barashkov; S A Fedorova; F M Teryutin; V L Akhmetova; I M Khidiyatova; R I Khusainova; S L Lobov; E K Khusnutdinova
Journal:  Acta Naturae       Date:  2011-07       Impact factor: 1.845

2.  Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.

Authors:  R L P Santos; M Wajid; T L Pham; J Hussan; G Ali; W Ahmad; S M Leal
Journal:  Clin Genet       Date:  2005-01       Impact factor: 4.438

3.  GJB2 mutations in Baluchi population.

Authors:  Anoosh Naghavi; Carla Nishimura; Kimia Kahrizi; Yasser Riazalhosseini; Niloofar Bazazzadegan; Marzieh Mohseni; Richard J H Smith; Hossein Najmabadi
Journal:  J Genet       Date:  2008-08       Impact factor: 1.166

4.  Prevalence of GJB2 gene mutations correlated to presence of clinical and environmental risk factors in the etiology of congenital sensorineural hearing loss of the Romanian population.

Authors:  Alexandra Neagu; Adela-Ioana Mocanu; Alexandru Bonciu; Gabriella Coadă; Horia Mocanu
Journal:  Exp Ther Med       Date:  2021-04-14       Impact factor: 2.447

Review 5.  The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.

Authors:  Denise Yan; Abhiraami Kannan-Sundhari; Subramanian Vishwanath; Jie Qing; Rahul Mittal; Mohan Kameswaran; Xue Zhong Liu
Journal:  Genet Test Mol Biomarkers       Date:  2015-07-17

6.  Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.

Authors:  Jiann-Jou Yang; Wen-Hung Wang; Yen-Chun Lin; Hsu-Huei Weng; Jen-Tsung Yang; Chung-Feng Hwang; Che-Min Wu; Shuan-Yow Li
Journal:  Hum Genet       Date:  2010-07-01       Impact factor: 4.132

Review 7.  Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL).

Authors:  Shivani Mishra; Himani Pandey; Priyanka Srivastava; Kausik Mandal; Shubha R Phadke
Journal:  Indian J Pediatr       Date:  2018-03-15       Impact factor: 1.967

8.  GJB2 and GJB6 gene mutations found in Indian probands with congenital hearing impairment.

Authors:  G Padma; P V Ramchander; U V Nandur; T Padma
Journal:  J Genet       Date:  2009-12       Impact factor: 1.166

9.  Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.

Authors:  Seyed Basir Hashemi; Mohamad Javad Ashraf; Mohamad Saboori; Negar Azarpira; Masumeh Darai
Journal:  Mol Biol Rep       Date:  2012-10-17       Impact factor: 2.316

10.  Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet University.

Authors:  Susan H Blanton; Walter E Nance; Virginia W Norris; Katherine O Welch; Amber Burt; Arti Pandya; Kathleen S Arnos
Journal:  Ann Hum Genet       Date:  2009-11-20       Impact factor: 1.670
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