New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8

Interpretation of Association Signals and Identification of Causal Variants from Genome-wide Association Studies

(2010) Kai Wang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

ProbABEL package for genome-wide association analysis of imputed data

(2010) Yurii S Aulchenko et al.   BMC BIOINFORMATICS

Rare Variants Create Synthetic Genome-Wide Associations

(2010) Samuel P. Dickson et al.   PLOS BIOLOGY

Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness

(2010) Yi Lu et al.   PLoS Genetics

TENUITY OF CORNEA WITH EHLERS-DANLOS SYNDROME

(2009) B. MOESTRUP   ACTA OPHTHALMOLOGICA

Genetic comparison of a Croatian isolate and CEPH European founders

(2009) Pau Navarro et al.   GENETIC EPIDEMIOLOGY

Ocular forkhead transcription factors: seeing eye to eye

(2009) Holly E. Moose et al.   INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY

Genome-wide association study identifies five loci associated with lung function

(2009) Emmanouela Repapi et al.   NATURE GENETICS

Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome

(2008) Almogit Abu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

(2008) A. D. Johnson et al.   BIOINFORMATICS

Development of the corneal stroma, and the collagen-proteoglycan associations that help define its structure and function

(2008) Andrew J. Quantock et al.   DEVELOPMENTAL DYNAMICS

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

(2008) Itsik Pe'er et al.   GENETIC EPIDEMIOLOGY