Vincent A - Search Results

1

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.

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

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.

Héon E, Greenberg A, Kopp KK, Rootman D, Vincent AL, Billingsley G, Priston M, Dorval KM, Chow RL, McInnes RR, Heathcote G, Westall C, Sutphin JE, Semina E, Bremner R, Stone EM. Héon E, et al. Among authors: vincent al. Hum Mol Genet. 2002 May 1;11(9):1029-36. doi: 10.1093/hmg/11.9.1029. Hum Mol Genet. 2002. PMID: 11978762

5

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.

6

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.

7

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.

8

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.

9

The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndrome.

Kletke S, Batmanabane V, Dai T, Vincent A, Li S, Gordon KA, Papsin BC, Cushing SL, Héon E. Kletke S, et al. Among authors: vincent a. Clin Genet. 2017 Jul;92(1):26-33. doi: 10.1111/cge.12895. Epub 2017 Jan 16. Clin Genet. 2017. PMID: 27743452

10

Specific retinal phenotype in early IQCB1-related disease.

Vincent A, AlAli A, MacDonald H, VandenHoven C, Héon E. Vincent A, et al. Eye (Lond). 2018 Mar;32(3):646-651. doi: 10.1038/eye.2017.283. Epub 2017 Dec 8. Eye (Lond). 2018. PMID: 29219953 Free PMC article.

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