Publications by authors named "Sharon A Jenkins"

Claim this Profile
G
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.
Valentina Cipriani, Hin-Tak Leung, Vincent Plagnol, Catey Bunce, Jane C Khan, Sharon A Jenkins

Hum Mol Genet· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.
Reecha Sofat, Juan P Casas, Andrew R Webster, Alan C Bird, Samantha S Mann, Sharon A Jenkins

Int J Epidemiol· February 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The symmetry of phenotype between eyes of patients with early and late bilateral age-related macular degeneration (AMD).
Samantha S Mann, Yvonne Rutishauser-Arnold, Tunde Peto, Sharon A Jenkins, Irene Leung

Graefes Arch Clin Exp Ophthalmol· February 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family members.
Michel Michaelides, Sharon A Jenkins, Doris-Eva Bamiou, Mary G Sweeney, Mary B Davis

Arch Ophthalmol· March 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?
Isabelle Audo, Olivier M Vanakker, Alaric Smith, Bart P Leroy, Anthony G Robson, Sharon A Jenkins

Invest Ophthalmol Vis Sci· September 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in the gene coding for the pre-mRNA splicing factor, PRPF31, in patients with autosomal dominant retinitis pigmentosa.
Naushin H Waseem, Veronika Vaclavik, Andrew Webster, Sharon A Jenkins, Alan C Bird

Invest Ophthalmol Vis Sci· March 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.
Huimin Wu, Jill A Cowing, Michel Michaelides, Susan E Wilkie, Glen Jeffery, Sharon A Jenkins

Am J Hum Genet· September 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunction.
Michel Michaelides, Sharon A Jenkins, Milam A Brantley, Richard M Andrews, Naushin Waseem

Invest Ophthalmol Vis Sci· July 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Autofluorescence imaging of choroidal neovascularization due to age-related macular degeneration.
Samantha S Dandekar, Sharon A Jenkins, Tunde Peto, Hendrik P N Scholl, Kulwant S Sehmi

Arch Ophthalmol· November 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.
Neil D Ebenezer, Michel Michaelides, Sharon A Jenkins, Isabelle Audo, Andrew R Webster

Invest Ophthalmol Vis Sci· June 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis