Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

(2013) Ching-Yu Cheng et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Molecular and clinical characterization of 25 individuals with exonic deletions ofNRXN1and comprehensive review of the literature

(2013) Frédérique Béna et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Education influences the role of genetics in myopia

(2013) Virginie J. M. Verhoeven et al.   EUROPEAN JOURNAL OF EPIDEMIOLOGY

Astigmatism and its role in emmetropization

(2013) Chea-su Kee   EXPERIMENTAL EYE RESEARCH

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

The E3-Ligase TRIM Family of Proteins Regulates Signaling Pathways Triggered by Innate Immune Pattern-Recognition Receptors

(2013) Gijs A. Versteeg et al.   IMMUNITY

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

Meta-analysis methods for genome-wide association studies and beyond

(2013) Evangelos Evangelou et al.   NATURE REVIEWS GENETICS

Genome-Wide Analysis Points to Roles for Extracellular Matrix Remodeling, the Visual Cycle, and Neuronal Development in Myopia

(2013) Amy K. Kiefer et al.   PLoS Genetics

Heritability of corneal refraction and corneal astigmatism: a population-based twin study among 66- to 79-year-old female twins

(2012) Olavi Pärssinen et al.   ACTA OPHTHALMOLOGICA

Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility

(2012) Mario Capasso et al.   CARCINOGENESIS

Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations

(2012) B. K. Cornes et al.   HUMAN MOLECULAR GENETICS

Cohort Profile: The Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort

(2012) A. Fraser et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Cohort Profile: The ‘Children of the 90s’—the index offspring of the Avon Longitudinal Study of Parents and Children

(2012) Andy Boyd et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Non-coding RNAs with essential roles in neurodegenerative disorders

(2012) Evgenia Salta et al.   LANCET NEUROLOGY

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

(2012) Bryan Howie et al.   NATURE GENETICS

The Rotterdam Study: 2012 objectives and design update

(2011) Albert Hofman et al.   EUROPEAN JOURNAL OF EPIDEMIOLOGY

UGT1A1 is a major locus influencing bilirubin levels in African Americans

(2011) Guanjie Chen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area

(2011) Chiea Chuen Khor et al.   HUMAN MOLECULAR GENETICS

Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore

(2011) Siyu Han et al.   HUMAN MOLECULAR GENETICS

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

(2011) Kathryn P Burdon et al.   NATURE GENETICS

Risk Factors for Astigmatism in Preschool Children

(2011) Roberta McKean-Cowdin et al.   OPHTHALMOLOGY

Human Cancer Long Non-Coding RNA Transcriptomes

(2011) Ewan A. Gibb et al.   PLoS One

Genome-Wide Meta-Analysis of Five Asian Cohorts Identifies PDGFRA as a Susceptibility Locus for Corneal Astigmatism

(2011) Qiao Fan et al.   PLoS Genetics

METAL: fast and efficient meta-analysis of genomewide association scans

(2010) C. J. Willer et al.   BIOINFORMATICS

Syndecan-1 regulates cell migration and fibronectin fibril assembly

(2010) Mary Ann Stepp et al.   EXPERIMENTAL CELL RESEARCH

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

(2010) Yun Li et al.   GENETIC EPIDEMIOLOGY

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels

(2010) Konrad Oexle et al.   HUMAN MOLECULAR GENETICS

Collagen-related genes influence the glaucoma risk factor, central corneal thickness

(2010) Eranga N. Vithana et al.   HUMAN MOLECULAR GENETICS

Hundreds of variants clustered in genomic loci and biological pathways affect human height

(2010) Hana Lango Allen 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

Heritability of Spherical Equivalent

(2010) Olavi Pärssinen et al.   OPHTHALMOLOGY

Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese

(2010) Yi-Ju Li et al.   OPHTHALMOLOGY

Myopia Over the Lifecourse: Prevalence and Early Life Influences in the 1958 British Birth Cohort

(2010) Jugnoo S. Rahi et al.   OPHTHALMOLOGY

A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose

(2009) A. D. Paterson et al.   DIABETES

Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals

(2009) Mitchell Guttman et al.   NATURE

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

(2009) Rosalind A Eeles et al.   NATURE GENETICS

KIBRA and CLSTN2 polymorphisms exert interactive effects on human episodic memory

(2009) Claudia Preuschhof et al.   NEUROPSYCHOLOGIA

The 25-Year Incidence of Visual Impairment in Type 1 Diabetes Mellitus

(2009) Ronald Klein et al.   OPHTHALMOLOGY

Genetic Structure of Europeans: A View from the North–East

(2009) Mari Nelis et al.   PLoS One

Neurexin 1 (NRXN1) Deletions in Schizophrenia

(2009) G. Kirov et al.   SCHIZOPHRENIA BULLETIN

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

Estimation of significance thresholds for genomewide association scans

(2008) Frank Dudbridge et al.   GENETIC EPIDEMIOLOGY

Cohort Profile: The Cardiovascular Risk in Young Finns Study

(2008) O. T Raitakari et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY