A. Rice

发表

Endothelial Cell Survival and Graft Profile Analysis in Descemet Stripping Endothelial Keratoplasty

S. Anand, J. Ball, A. Rice, 2011, Cornea.

Replication of the recessive STBMS1 locus but with dominant inheritance.

Brendan T Barrett, David B Elliott, Eamonn Sheridan, 2009, Investigative ophthalmology & visual science.

Mutational analysis of MIR184 in sporadic keratoconus and myopia.

P. Mitchell, C. Willoughby, R. Mills, 2013, Investigative ophthalmology & visual science.

A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus

Bennet J. McComish, R. Krauss, C. Klaver, 2021, Communications Biology.

Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus.

A. Wright, V. Vitart, D. Armstrong, 2014, Human molecular genetics.

Mid-term outcomes of penetrating keratoplasty (PK) and deep anterior lamellar keratoplasty (DALK)

K. Pesudovs, J. Ball, A. Rice, 2009, Eye.

Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome

C. Inglehearn, C. Toomes, Manir Ali, 2013, Cornea.

Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacity.

Colin A. Johnson, A. Markham, M. Mohamed, 2011, Investigative ophthalmology & visual science.

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma

M. McKibbin, C. Inglehearn, N. Fernandez-Fuentes, 2010, Molecular vision.

Novel mutations in the small leucine‐rich repeat protein/proteoglycan (SLRP) genes in high myopia

T. Spector, L. Ala‐Kokko, C. Hammond, 2007, Human mutation.

Solitary Langerhans cell histiocytosis in association with primary biliary cirrhosis

J. Wyatt, A. Rice, 2000, Histopathology.

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.

D. Mackey, K. Hayashi, A. Markham, 2010, American journal of human genetics.

Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome

C. Inglehearn, C. Toomes, Manir Ali, 2013, Cornea.

Replication of the recessive STBMS1 locus but with dominant inheritance.

C. Inglehearn, C. Toomes, E. Sheridan, 2009, Investigative ophthalmology & visual science.