Literature DB >> 12876827

Epidemiology of hereditary ocular disorders.

Thomas Rosenberg1.   

Abstract

Molecular genetic evidence has contributed significantly to the understanding of the fundamental molecular biology of the eye in health and disease, but it has also exposed the inadequacy of our traditional clinically based classification of hereditary eye disorders by unravelling significant genetic non-allelic heterogeneity in many eye disorders. Furthermore, our understanding of the epidemiology of hereditary ocular disorders has gained considerably by the establishment of mutation spectra in a rapidly growing number of monogenic eye disorders. In this overview, special emphasis has been put on the growing impact of genetic eye diseases in visual impairment, genetic heterogeneity, and the role of founder mutations for the skewed appearance of certain hereditary ocular disorders in some populations.

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Year:  2003        PMID: 12876827     DOI: 10.1159/000072036

Source DB:  PubMed          Journal:  Dev Ophthalmol        ISSN: 0250-3751


  18 in total

1.  Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa.

Authors:  Dikla Bandah-Rozenfeld; Rob W J Collin; Eyal Banin; L Ingeborgh van den Born; Karlien L M Coene; Anna M Siemiatkowska; Lina Zelinger; Muhammad I Khan; Dirk J Lefeber; Inbar Erdinest; Francesco Testa; Francesca Simonelli; Krysta Voesenek; Ellen A W Blokland; Tim M Strom; Caroline C W Klaver; Raheel Qamar; Sandro Banfi; Frans P M Cremers; Dror Sharon; Anneke I den Hollander
Journal:  Am J Hum Genet       Date:  2010-07-30       Impact factor: 11.025

2.  Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.

Authors:  Prasanthi Namburi; Rinki Ratnapriya; Samer Khateb; Csilla H Lazar; Yael Kinarty; Alexey Obolensky; Inbar Erdinest; Devorah Marks-Ohana; Eran Pras; Tamar Ben-Yosef; Hadas Newman; Menachem Gross; Anand Swaroop; Eyal Banin; Dror Sharon
Journal:  Am J Hum Genet       Date:  2016-09-01       Impact factor: 11.025

Review 3.  Regulation of dolichol-linked glycosylation.

Authors:  Michael Welti
Journal:  Glycoconj J       Date:  2012-06-21       Impact factor: 2.916

4.  Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa.

Authors:  Dikla Bandah-Rozenfeld; Liliana Mizrahi-Meissonnier; Chen Farhy; Alexey Obolensky; Itay Chowers; Jacob Pe'er; Saul Merin; Tamar Ben-Yosef; Ruth Ashery-Padan; Eyal Banin; Dror Sharon
Journal:  Am J Hum Genet       Date:  2010-08-12       Impact factor: 11.025

5.  A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews.

Authors:  Lina Zelinger; Eyal Banin; Alexey Obolensky; Liliana Mizrahi-Meissonnier; Avigail Beryozkin; Dikla Bandah-Rozenfeld; Shahar Frenkel; Tamar Ben-Yosef; Saul Merin; Sharon B Schwartz; Artur V Cideciyan; Samuel G Jacobson; Dror Sharon
Journal:  Am J Hum Genet       Date:  2011-02-03       Impact factor: 11.025

6.  Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B.

Authors:  Samer Khateb; Marco Nassisi; Kinga M Bujakowska; Cécile Méjécase; Christel Condroyer; Aline Antonio; Marine Foussard; Vanessa Démontant; Saddek Mohand-Saïd; José-Alain Sahel; Christina Zeitz; Isabelle Audo
Journal:  JAMA Ophthalmol       Date:  2019-06-01       Impact factor: 7.389

7.  A novel mutation in RDH5 gene causes retinitis pigmentosa in consanguineous Pakistani family.

Authors:  Neelam Sultan; Irfan Ali; Shazia Anwer Bukhari; Shahid Mahmood Baig; Muhammad Asif; Muhammad Qasim; Muhammad Imran Naseer; Mahmood Rasool
Journal:  Genes Genomics       Date:  2018-02-03       Impact factor: 1.839

8.  The efficacy of microarray screening for autosomal recessive retinitis pigmentosa in routine clinical practice.

Authors:  Ramon A C van Huet; Laurence H M Pierrache; Magda A Meester-Smoor; Caroline C W Klaver; L Ingeborgh van den Born; Carel B Hoyng; Ilse J de Wijs; Rob W J Collin; Lies H Hoefsloot; B Jeroen Klevering
Journal:  Mol Vis       Date:  2015-04-28       Impact factor: 2.367

9.  Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations.

Authors:  Dror Sharon; Eyal Banin
Journal:  Mol Vis       Date:  2015-07-17       Impact factor: 2.367

10.  Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies.

Authors:  Avigail Beryozkin; Elia Shevah; Adva Kimchi; Liliana Mizrahi-Meissonnier; Samer Khateb; Rinki Ratnapriya; Csilla H Lazar; Anat Blumenfeld; Tamar Ben-Yosef; Yitzhak Hemo; Jacob Pe'er; Eduard Averbuch; Michal Sagi; Alexis Boleda; Linn Gieser; Abraham Zlotogorski; Tzipora Falik-Zaccai; Ola Alimi-Kasem; Samuel G Jacobson; Itay Chowers; Anand Swaroop; Eyal Banin; Dror Sharon
Journal:  Sci Rep       Date:  2015-08-26       Impact factor: 4.379

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