Green JS - Search Results

1

Hereditary diseases as causes of blindness in Newfoundland: preliminary report.

Green JS, Johnson GJ. Green JS, et al. Can J Ophthalmol. 1983 Oct;18(6):281-4. Can J Ophthalmol. 1983. PMID: 6652573

2

Prevention of blindness due to genetic disease.

Johnson GJ, Green JS. Johnson GJ, et al. Among authors: green js. Can J Ophthalmol. 1987 Apr;22(3):145-51. Can J Ophthalmol. 1987. PMID: 3474048 No abstract available.

3

Survey of ophthalmic conditions in a Labrador community: II. Ocular disease.

Johnson GJ, Green JS, Paterson GD, Perkins ES. Johnson GJ, et al. Among authors: green js. Can J Ophthalmol. 1984 Aug;19(5):224-33. Can J Ophthalmol. 1984. PMID: 6478308

4

The burden of genetically determined eye disease.

Green JS, Bear JC, Johnson GJ. Green JS, et al. Br J Ophthalmol. 1986 Sep;70(9):696-9. doi: 10.1136/bjo.70.9.696. Br J Ophthalmol. 1986. PMID: 3756127 Free PMC article.

5

Von Hippel-Lindau disease in a Newfoundland kindred.

Green JS, Bowmer MI, Johnson GJ. Green JS, et al. CMAJ. 1986 Jan 15;134(2):133-8, 146. CMAJ. 1986. PMID: 3942913 Free PMC article.

6

Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1.

Eichers ER, Green JS, Stockton DW, Jackman CS, Whelan J, McNamara JA, Johnson GJ, Lupski JR, Katsanis N. Eichers ER, et al. Among authors: green js. Am J Hum Genet. 2002 Apr;70(4):955-64. doi: 10.1086/339688. Epub 2002 Feb 26. Am J Hum Genet. 2002. PMID: 11868161 Free PMC article.

7

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly.

Doucette L, Green J, Fernandez B, Johnson GJ, Parfrey P, Young TL. Doucette L, et al. Eur J Hum Genet. 2011 Mar;19(3):293-9. doi: 10.1038/ejhg.2010.210. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150893 Free PMC article.

8

Molecular genetics of achromatopsia in Newfoundland reveal genetic heterogeneity, founder effects and the first cases of Jalili syndrome in North America.

Doucette L, Green J, Black C, Schwartzentruber J, Johnson GJ, Galutira D, Young TL. Doucette L, et al. Ophthalmic Genet. 2013 Sep;34(3):119-29. doi: 10.3109/13816810.2013.763993. Epub 2013 Jan 30. Ophthalmic Genet. 2013. PMID: 23362848

9

Congenital cataract with microcornea and Peters' anomaly as expressions of one autosomal dominant gene.

Green JS, Johnson GJ. Green JS, et al. Ophthalmic Paediatr Genet. 1986 Dec;7(3):187-94. doi: 10.3109/13816818609004137. Ophthalmic Paediatr Genet. 1986. PMID: 3550563

10

Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression.

Evans DR, Green JS, Johnson GJ, Schwartzentruber J, Majewski J, Beaulieu CL, Qin W, Marshall CR, Paton TA, Roslin NM, Paterson AD, Fahiminiya S, French J, Boycott KM, Woods MO; FORGE Canada Consortium. Evans DR, et al. Among authors: green js. Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1736-1742. doi: 10.1167/iovs.16-20864. Invest Ophthalmol Vis Sci. 2017. PMID: 28324114

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