Related references
Note: Only part of the references are listed.Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Milly S. Tedja et al.
NATURE GENETICS (2018)
CCDC102B confers risk of low vision and blindness in high myopia
Yoshikatsu Hosoda et al.
NATURE COMMUNICATIONS (2018)
WHAT IS THE FUNDAMENTAL NATURE OF PATHOLOGIC MYOPIA?
Kyoko Ohno-Matsui
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES (2017)
Association between Ocular Axial Length-Related Genes and High Myopia in a Han Chinese Population
Ya-Ting Li et al.
OPHTHALMOLOGICA (2016)
When do myopia genes have their effect? Comparison of genetic risks between children and adults
J. Willem L. Tideman et al.
GENETIC EPIDEMIOLOGY (2016)
Detection and interpretation of shared genetic influences on 42 human traits
Joseph K. Pickrell et al.
NATURE GENETICS (2016)
Global Prevalence of Myopia and High Myopia and Temporal Trends from 2000 through 2050
Brien A. Holden et al.
OPHTHALMOLOGY (2016)
Updates of pathologic myopia
Kyoko Ohno-Matsui et al.
PROGRESS IN RETINAL AND EYE RESEARCH (2016)
Epidemiology of Pathologic Myopia in Asia and Worldwide
Yee-Ling Wong et al.
ASIA-PACIFIC JOURNAL OF OPHTHALMOLOGY (2016)
International Photographic Classification and Grading System for Myopic Maculopathy
Kyoko Ohno-Matsui et al.
AMERICAN JOURNAL OF OPHTHALMOLOGY (2015)
The Rotterdam Study: 2016 objectives and design update
Albert Hofman et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2015)
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia
Masahiro Miyake et al.
NATURE COMMUNICATIONS (2015)
Evaluating the Association between Pathological Myopia and SNPs in RASGRFI, ACTCI and GJD2 Genes at Chromosome 15q14 and 15q25 in a Chinese Population
Chong-da Chen et al.
OPHTHALMIC GENETICS (2015)
The Ophthalmic Branch of the Gutenberg Health Study: Study Design, Cohort Profile and Self-Reported Diseases
Rene Hoehn et al.
PLOS ONE (2015)
Epidemiology and Disease Burden of Pathologic Myopia and Myopic Choroidal Neovascularization: An Evidence-Based Systematic Review
Tien Y. Wong et al.
AMERICAN JOURNAL OF OPHTHALMOLOGY (2014)
Association study of 15q14 and 15q25 with high myopia in the Han Chinese population
Yu Qiang et al.
BMC GENETICS (2014)
Genome-Wide Association Studies of Refractive Error and Myopia, Lessons Learned, and Implications for the Future
Pirro G. Hysi et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2014)
Comprehensive Replication of the Relationship Between Myopia-Related Genes and Refractive Errors in a Large Japanese Cohort
Munemitsu Yoshikawa et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2014)
The Rotterdam Study: 2014 objectives and design update
Albert Hofman et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2013)
An updated view on the role of dopamine in myopia
Marita Feldkaemper et al.
EXPERIMENTAL EYE RESEARCH (2013)
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
Dwight Stambolian et al.
HUMAN MOLECULAR GENETICS (2013)
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
Yi Shi et al.
HUMAN MOLECULAR GENETICS (2013)
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Chiea Chuen Khor et al.
HUMAN MOLECULAR GENETICS (2013)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Virginie J. M. Verhoeven et al.
NATURE GENETICS (2013)
Genetic Association of Refractive Error and Axial Length with 15q14 but Not 15q25 in the Blue Mountains Eye Study Cohort
Maria Schache et al.
OPHTHALMOLOGY (2013)
Genome-Wide Analysis Points to Roles for Extracellular Matrix Remodeling, the Visual Cycle, and Neuronal Development in Myopia
Amy K. Kiefer et al.
PLOS GENETICS (2013)
Association Between ZIC2, RASGRF1, and SHISA6 Genes and High Myopia in Japanese Subjects
Maho Oishi et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2013)
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium
Virginie J. M. Verhoeven et al.
HUMAN GENETICS (2012)
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
Bryan Howie et al.
NATURE GENETICS (2012)
Common variants in chromosome 4q25 are associated with myopia in Chinese adults
Yang Gao et al.
OPHTHALMIC AND PHYSIOLOGICAL OPTICS (2012)
Polymorphisms in the CTNND2 Gene and 11q24.1 Genomic Region Are Associated with Pathological Myopia in a Chinese Population
Zhiqiang Yu et al.
OPHTHALMOLOGICA (2012)
Genetic Variants on Chromosome 1q41 Influence Ocular Axial Length and High Myopia
Qiao Fan et al.
PLOS GENETICS (2012)
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
Weihua Meng et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2012)
The Rotterdam Study: 2012 objectives and design update
Albert Hofman et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2011)
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
Zhiqiang Li et al.
HUMAN MOLECULAR GENETICS (2011)
Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese
Yi-Ju Li et al.
OPHTHALMOLOGY (2011)
Modulation of rod photoreceptor output by HCN1 channels is essential for regular mesopic cone vision
Mathias W. Seeliger et al.
NATURE COMMUNICATIONS (2011)
Replication Study Supports CTNND2 as a Susceptibility Gene for High Myopia
Boyu Lu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)
Association of 15q14 and 15q25 with High Myopia in Japanese
Hisako Hayashi et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)
METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
BIOINFORMATICS (2010)
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25
Pirro G. Hysi et al.
NATURE GENETICS (2010)
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Abbas M. Solouki et al.
NATURE GENETICS (2010)
Expression of connexin genes in the human retina
Goran Soehl et al.
BMC OPHTHALMOLOGY (2010)
The Rotterdam Study: 2010 objectives and design update
Albert Hofman et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2009)
Connexin36, an Essential Element in the Rod Pathway, Is Highly Expressed in the Essentially Rodless Retina of Gallus gallus
A. H. Kihara et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2009)
RasGRF1 disruption causes retinal photoreception defects and associated transcriptomic alterations
Alberto Fernandez-Medarde et al.
JOURNAL OF NEUROCHEMISTRY (2009)
BK channels modulate pre- and postsynaptic signaling at reciprocal synapses in retina
William N. Grimes et al.
NATURE NEUROSCIENCE (2009)
The diverse functional roles and regulation of neuronal gap junctions in the retina
Stewart A. Bloomfield et al.
NATURE REVIEWS NEUROSCIENCE (2009)
Methodology of the Singapore Indian Chinese Cohort (SICC) Eye Study: Quantifying ethnic variations in the epidemiology of eye diseases in Asians
Raghavan Lavanya et al.
OPHTHALMIC EPIDEMIOLOGY (2009)
A Genome-Wide Association Analysis Identified a Novel Susceptible Locus for Pathological Myopia at 11q24.1
Hideo Nakanishi et al.
PLOS GENETICS (2009)
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
Bryan N. Howie et al.
PLOS GENETICS (2009)
The Rotterdam Study: Objectives and design update
Albert Hofman et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2007)
Ion channels in the RPE
Soenke Wimmers et al.
PROGRESS IN RETINAL AND EYE RESEARCH (2007)
Rationale and methodology for a population-based study of eye diseases in Malay people: The Singapore Malay eye study (SiMES)
Athena W. P. Foong et al.
OPHTHALMIC EPIDEMIOLOGY (2007)
Prevalence and causes of low vision and blindness in a Japanese adult population - The Tajimi Study
Aiko Iwase et al.
OPHTHALMOLOGY (2006)
Immunolocalization of the Ca2+-activated K+ channel Slo1 in axons and nerve terminals of mammalian brain and cultured neurons
H Misonou et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2006)
Prevalence of visual impairment among adults in China: The Beijing eye study
L Xu et al.
AMERICAN JOURNAL OF OPHTHALMOLOGY (2006)
Different functional types of bipolar cells use different gap-junctional proteins
B Lin et al.
JOURNAL OF NEUROSCIENCE (2005)
BRCC2, a novel BH3-like domain-containing protein, induces apoptosis in a caspase-dependent manner
CG Broustas et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Connexin36 is essential for transmission of rod-mediated visual signals in the mammalian retina
MR Deans et al.
NEURON (2002)
Visual transmission deficits in mice with targeted disruption of the gap junction gene connexin36
M Güldenagel et al.
JOURNAL OF NEUROSCIENCE (2001)
Share Paper
