Literature DB >> 19005985

Genetic isolates in ophthalmic diseases.

Justin C Sherwin1, Alex W Hewitt, Jonathan B Ruddle, David A Mackey.   

Abstract

In recent years, noteworthy gains have been made in unravelling the genetic contribution to some complex ocular diseases, principally age-related macular degeneration. Yet, a relatively poor understanding of the genetic aetiology for many other heritable blinding diseases, such as glaucoma, keratoconus and myopia, remains. Genetic isolates, populations with varying degrees of geographical or cultural seclusion, provide an effective means for investigating the molecular mechanisms involved in human diseases. This is particularly true for rare diseases in which founded alleles can be rapidly driven to a high frequency due to restriction of gene flow in the population. Recent success in complex gene mapping has resulted from the widened linkage disequilibrium (LD) in the genome of genetically isolated populations. An improved understanding of the predisposing genetic risk factors allows for enhanced screening modalities and paves the foundations for the translation of genomic technology into the clinic. This review focuses on the role population isolates have had in the investigation of genes underlying complex eye diseases and discusses their likely usefulness given the expansion of large-scale case-control association studies.

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Year:  2008        PMID: 19005985     DOI: 10.1080/13816810802334341

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  7 in total

1.  Distribution of conjunctival ultraviolet autofluorescence in a population-based study: the Norfolk Island Eye Study.

Authors:  J C Sherwin; A W Hewitt; L S Kearns; M T Coroneo; L R Griffiths; D A Mackey
Journal:  Eye (Lond)       Date:  2011-04-15       Impact factor: 3.775

Review 2.  Review and update on the molecular basis of Leber congenital amaurosis.

Authors:  Oscar Francisco Chacon-Camacho; Juan Carlos Zenteno
Journal:  World J Clin Cases       Date:  2015-02-16       Impact factor: 1.337

3.  Phenotype-genotype correlation with Sanger sequencing identified retinol dehydrogenase 12 (RDH12) compound heterozygous variants in a Chinese family with Leber congenital amaurosis.

Authors:  Yun Li; Qing Pan; Yang-Shun Gu
Journal:  J Zhejiang Univ Sci B       Date:  2017-05       Impact factor: 3.066

4.  Ophthalmic genetics: moving forward.

Authors:  Khaled K Abu-Amero
Journal:  Middle East Afr J Ophthalmol       Date:  2011-01

5.  An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican village.

Authors:  Carlos Pantoja-Melendez; Manir Ali; Juan C Zenteno
Journal:  Mol Vis       Date:  2013-08-27       Impact factor: 2.367

Review 6.  Genetic Aspects of Keratoconus: A Literature Review Exploring Potential Genetic Contributions and Possible Genetic Relationships with Comorbidities.

Authors:  Eleftherios Loukovitis; Konstantinos Sfakianakis; Panagiota Syrmakesi; Eleni Tsotridou; Myrsini Orfanidou; Dimitra Rafailia Bakaloudi; Maria Stoila; Athina Kozei; Spyridon Koronis; Zachos Zachariadis; Paris Tranos; Nikos Kozeis; Miltos Balidis; Zisis Gatzioufas; Aliki Fiska; George Anogeianakis
Journal:  Ophthalmol Ther       Date:  2018-09-06

7.  High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.

Authors:  Petra Liskova; Rhian Gwilliam; Martin Filipec; Katerina Jirsova; Stanislava Reinstein Merjava; Panos Deloukas; Tom R Webb; Shomi S Bhattacharya; Neil D Ebenezer; Alex G Morris; Alison J Hardcastle
Journal:  PLoS One       Date:  2012-09-25       Impact factor: 3.240

  7 in total

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