Exome sequencing reveals CCDC111 mutation associated with high myopia

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

(2013) Dwight Stambolian et al.   HUMAN MOLECULAR GENETICS

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population

(2013) Y. Shi et al.   HUMAN MOLECULAR GENETICS

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

(2013) Virginie J M Verhoeven et al.   NATURE GENETICS

Myopia

(2012) Ian G Morgan et al.   LANCET

Genetic Variants on Chromosome 1q41 Influence Ocular Axial Length and High Myopia

(2012) Qiao Fan et al.   PLoS Genetics

Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population

(2011) Yi Shi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population

(2011) Zhiqiang Li et al.   HUMAN MOLECULAR GENETICS

Exome Sequencing Identifies ZNF644 Mutations in High Myopia

(2011) Yi Shi et al.   PLoS Genetics

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing

(2010) Jun Ling Wang et al.   BRAIN

X-linked myopia: Bornholm Eye Disease

(2010) Marianne Schwartz et al.   CLINICAL GENETICS

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

(2010) Kaya Bilgüvar et al.   NATURE

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25

(2010) Pirro G Hysi et al.   NATURE GENETICS

A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14

(2010) Abbas M Solouki et al.   NATURE GENETICS

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

(2010) Alexander Hoischen et al.   NATURE GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Increased Prevalence of Myopia in the United States Between 1971-1972 and 1999-2004

(2009) Susan Vitale   ARCHIVES OF OPHTHALMOLOGY

Targeted capture and massively parallel sequencing of 12 human exomes

(2009) Sarah B. Ng et al.   NATURE

Exome sequencing identifies the cause of a mendelian disorder

(2009) Sarah B Ng et al.   NATURE GENETICS

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity

(2009) H D Hosgood et al.   OCCUPATIONAL AND ENVIRONMENTAL MEDICINE

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

(2009) Murim Choi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Genome-Wide Association Analysis Identified a Novel Susceptible Locus for Pathological Myopia at 11q24.1

(2009) Hideo Nakanishi et al.   PLoS Genetics

Refractive Errors in an Elderly Japanese Population

(2008) Akira Sawada et al.   OPHTHALMOLOGY

Prevalence of Myopia in Urban and Rural Children in Mainland China

(2008) Mingguang He et al.   OPTOMETRY AND VISION SCIENCE