Vincent A - Search Results

1

Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 Patients.

Heath Jeffery RC, Thompson JA, Lo J, Chelva ES, Armstrong S, Pulido JS, Procopio R, Vincent AL, Bianco L, Battaglia Parodi M, Ziccardi L, Antonelli G, Barbano L, Marques JP, Geada S, Carvalho AL, Tang WC, Chan CM, Boon CJF, Hensman J, Chen TC, Lin CY, Chen PL, Vincent A, Tumber A, Heon E, Grigg JR, Jamieson RV, Cornish EE, Nash BM, Borooah S, Ayton LN, Britten-Jones AC, Edwards TL, Ruddle JB, Sharma A, Porter RG, Lamey TM, McLaren TL, McLenachan S, Roshandel D, Chen FK. Heath Jeffery RC, et al. Among authors: vincent a, vincent al. Invest Ophthalmol Vis Sci. 2024 May 1;65(5):22. doi: 10.1167/iovs.65.5.22. Invest Ophthalmol Vis Sci. 2024. PMID: 38743414 Free PMC article.

2

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.

Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Héon E. Vincent AL, et al. Am J Hum Genet. 2002 Feb;70(2):448-60. doi: 10.1086/338709. Epub 2002 Jan 3. Am J Hum Genet. 2002. PMID: 11774072 Free PMC article.

3

Prosthetic conformers: a step towards improved rehabilitation of enucleated children.

Vincent AL, Webb MC, Gallie BL, Héon E. Vincent AL, et al. Clin Exp Ophthalmol. 2002 Feb;30(1):58-9. doi: 10.1046/j.1442-9071.2002.00472.x. Clin Exp Ophthalmol. 2002. PMID: 11887800

4

A molecular perspective on corneal dystrophies.

Vincent AL, Rootman D, Munier FL, Héon E. Vincent AL, et al. Dev Ophthalmol. 2003;37:50-66. doi: 10.1159/000072038. Dev Ophthalmol. 2003. PMID: 12876829 Review.

5

Further support of the role of CYP1B1 in patients with Peters anomaly.

Vincent A, Billingsley G, Priston M, Glaser T, Oliver E, Walter M, Ritch R, Levin A, Heon E. Vincent A, et al. Mol Vis. 2006 May 16;12:506-10. Mol Vis. 2006. PMID: 16735991 Free article.

6

Genetic analysis of chromosome 20-related posterior polymorphous corneal dystrophy: genetic heterogeneity and exclusion of three candidate genes.

Hosseini SM, Herd S, Vincent AL, Héon E. Hosseini SM, et al. Mol Vis. 2008 Jan 16;14:71-80. Mol Vis. 2008. PMID: 18253095 Free PMC article.

7

An audit of genetic testing in diagnosis of inherited retinal disorders: a prerequisite for gene-specific intervention.

Pradhan M, Hayes I, Vincent A. Pradhan M, et al. Among authors: vincent a. Clin Exp Ophthalmol. 2009 Sep;37(7):703-11. doi: 10.1111/j.1442-9071.2009.02129.x. Clin Exp Ophthalmol. 2009. PMID: 19788668

8

TGFBI mutational analysis in a New Zealand population of inherited corneal dystrophy patients.

Vincent AL, de Karolyi B, Patel DV, Wheeldon CE, McGhee CN. Vincent AL, et al. Br J Ophthalmol. 2010 Jul;94(7):836-42. doi: 10.1136/bjo.2009.159632. Epub 2009 Nov 30. Br J Ophthalmol. 2010. PMID: 19948560

9

Vincent A, McAlister C, Vandenhoven C, Héon E. Vincent A, et al. Eye (Lond). 2011 Jan;25(1):113-8. doi: 10.1038/eye.2010.165. Epub 2010 Nov 12. Eye (Lond). 2011. PMID: 21072067 Free PMC article.

10

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

Vincent A, Héon E. Vincent A, et al. Eye (Lond). 2012 Sep;26(9):1278-80. doi: 10.1038/eye.2012.125. Epub 2012 Jun 29. Eye (Lond). 2012. PMID: 22744390 Free PMC article. No abstract available.

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