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

Rapid inexpensive genome-wide association using pooled whole blood

(2009) J. E. Craig et al.   GENOME RESEARCH

Geographical structure and differential natural selection among North European populations

(2009) B. P. McEvoy et al.   GENOME RESEARCH

Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins

(2009) David A. Mackey et al.   Twin Research and Human Genetics

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics

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

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

Common sequence variants on 20q11.22 confer melanoma susceptibility

(2008) Kevin M Brown et al.   NATURE GENETICS

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays

(2008) S. Macgregor et al.   NUCLEIC ACIDS RESEARCH