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Literature DB >> 15635082

Identification of a new locus for isolated familial keratoconus at 2p24.

H Hutchings, H Ginisty, M Le Gallo, D Levy, F Stoësser, J F Rouland, J L Arné, M H Lalaux, P Calvas, M P Roth, A Hovnanian, F Malecaze.

Abstract

Mesh：

Year: 2005 PMID： 15635082 PMCID： PMC1735904 DOI： 10.1136/jmg.2004.022103

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

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34 in total

1. A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.

Authors: Xiaohui Li; Yelena Bykhovskaya; Talin Haritunians; David Siscovick; Anthony Aldave; Loretta Szczotka-Flynn; Sudha K Iyengar; Jerome I Rotter; Kent D Taylor; Yaron S Rabinowitz
Journal: Hum Mol Genet Date: 2011-10-06 Impact factor: 6.150

2. Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus.

Authors: Kathryn P Burdon; Stuart Macgregor; Yelena Bykhovskaya; Sharhbanou Javadiyan; Xiaohui Li; Kate J Laurie; Dorota Muszynska; Richard Lindsay; Judith Lechner; Talin Haritunians; Anjali K Henders; Durga Dash; David Siscovick; Seema Anand; Anthony Aldave; Douglas J Coster; Loretta Szczotka-Flynn; Richard A Mills; Sudha K Iyengar; Kent D Taylor; Tony Phillips; Grant W Montgomery; Jerome I Rotter; Alex W Hewitt; Shiwani Sharma; Yaron S Rabinowitz; Colin Willoughby; Jamie E Craig
Journal: Invest Ophthalmol Vis Sci Date: 2011-10-31 Impact factor: 4.799

3. Longitudinal study of keratoconus progression.

Authors: Xiaohui Li; Huiying Yang; Yaron S Rabinowitz
Journal: Exp Eye Res Date: 2007-07-06 Impact factor: 3.467

4. Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

Authors: Kathryn P Burdon; Douglas J Coster; Jac C Charlesworth; Richard A Mills; Kate J Laurie; Cecilia Giunta; Alex W Hewitt; Paul Latimer; Jamie E Craig
Journal: Hum Genet Date: 2008-09-05 Impact factor: 4.132

5. Optical coherence tomography combined with videokeratography to differentiate mild keratoconus subtypes.

Authors: Yaron S Rabinowitz; Xiaohui Li; Ana Laura Caiado Canedo; Renato Ambrósio; Yelena Bykhovskaya
Journal: J Refract Surg Date: 2014-02 Impact factor: 3.573

6. Classification of posterior polymorphous corneal dystrophy as a corneal ectatic disorder following confirmation of associated significant corneal steepening.

Authors: Anthony J Aldave; Lydia B Ann; Ricardo F Frausto; Catherine K Nguyen; Fei Yu; Irving M Raber
Journal: JAMA Ophthalmol Date: 2013-12 Impact factor: 7.389

Identification of a new locus for isolated familial keratoconus at 2p24.

1. A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.

2. Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus.

3. Longitudinal study of keratoconus progression.

4. Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

5. Optical coherence tomography combined with videokeratography to differentiate mild keratoconus subtypes.

6. Classification of posterior polymorphous corneal dystrophy as a corneal ectatic disorder following confirmation of associated significant corneal steepening.

7. Keratoconus: overview and update on treatment.

8. Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus.

9. VSX1 gene variants are associated with keratoconus in unrelated Korean patients.

10. Molecular analysis of the VSX1 gene in familial keratoconus.