Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract.
暂无分享,去创建一个
Y. Teo | P. Mitchell | J. Jonas | T. Wong | Liang Xu | E. Tai | Yingfeng Zheng | Jie-Jin Wang | B. Klein | S. Saw | G. Jun | Ching-Yu Cheng | T. Aung | C. Khor | Y. X. Wang | Xinyi Su | Xiang Li | W. Tay | Peng Chen | Xu Wang | E. Vithana | Merwyn Chew | S. Iyengar | Jiemin Liao | A. Tan | L. Thean | V. Barathi | Q. Tan | Clement Tan | T. Wong | T. Wong | Xu Wang | T. Wong | T. Wong
[1] Vanita Gupta,et al. Specific activation of the glucocorticoid receptor and modulation of signal transduction pathways in human lens epithelial cells. , 2007, Investigative ophthalmology & visual science.
[2] A. Riess,et al. Identification of a novel CRYBB2 missense mutation causing congenital autosomal dominant cataract , 2012, Molecular vision.
[3] D. Pascolini,et al. Global estimates of visual impairment: 2010 , 2011, British Journal of Ophthalmology.
[4] L. Fan,et al. Down‐regulation and CpG island hypermethylation of CRYAA in age‐related nuclear cataract , 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[5] O. Pongs,et al. Structural and Functional Characterization of Human Potassium Channel Subunit β1 (KCNA1B) , 1996, Neuropharmacology.
[6] Eleazar Eskin,et al. Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. , 2011, American journal of human genetics.
[7] Evangelos Evangelou,et al. Heterogeneity in Meta-Analyses of Genome-Wide Association Investigations , 2007, PloS one.
[8] U. Andley. Effects of α-Crystallin on Lens Cell Function and Cataract Pathology , 2009 .
[9] K. Nishida,et al. MAPK activation in mature cataract associated with Noonan syndrome , 2013, BMC Ophthalmology.
[10] U. Andley. Effects of alpha-crystallin on lens cell function and cataract pathology. , 2009, Current molecular medicine.
[11] M. C. Leske,et al. The Lens Opacities Classification System III. The Longitudinal Study of Cataract Study Group. , 1993, Archives of ophthalmology.
[12] David J Lee,et al. Effects of smoking on ocular health , 2011, Current opinion in ophthalmology.
[13] U. Andley,et al. Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q , 2003, European Journal of Human Genetics.
[14] Rick Twee-Hee Ong,et al. varLD: a program for quantifying variation in linkage disequilibrium patterns between populations , 2010, Bioinform..
[15] Stuart G. Parker,et al. The age-related eye disease study (AREDS) system for classifying cataracts from photographs: AREDS report no. 4. , 2001, American journal of ophthalmology.
[16] Ching-Yu Cheng,et al. Epidemiologic study of age-related cataracts among an elderly Chinese population in Shih-Pai, Taiwan. , 2003, Ophthalmology.
[17] Y. Kanai,et al. Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities , 1999, Nature Genetics.
[18] K L Linton,et al. Assessment of cataracts from photographs in the Beaver Dam Eye Study. , 1990, Ophthalmology.
[19] T. Wong,et al. Rationale and Methodology for a Population-Based Study of Eye Diseases in Malay People: The Singapore Malay Eye Study (SiMES) , 2007, Ophthalmic epidemiology.
[20] I. Sibon,et al. Ophthalmological features associated with COL4A1 mutations. , 2010, Archives of ophthalmology.
[21] P. Denis,et al. New phenotype associated with an Arg116Cys mutation in the CRYAA gene: nuclear cataract, iris coloboma, and microphthalmia. , 2007, Archives of ophthalmology.
[22] Hong Zhang,et al. Proteomic analysis of human age-related nuclear cataracts and normal lens nuclei. , 2011, Investigative ophthalmology & visual science.
[23] P. Sham,et al. A Knowledge-Based Weighting Framework to Boost the Power of Genome-Wide Association Studies , 2010, PloS one.
[24] Structural and functional characterization of human potassium channel subunit beta 1 (KCNA1B). , 1996, Neuropharmacology.
[25] Peng Chen,et al. Deep whole-genome sequencing of 100 southeast Asian Malays. , 2013, American journal of human genetics.
[26] K. Sperling,et al. Novel mutation in the γ-S crystallin gene causing autosomal dominant cataract , 2009, Molecular vision.
[27] N. Niikawa,et al. CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20q. , 2007, American journal of human genetics.
[28] Jost B Jonas,et al. Five-year incidence of age-related cataract and cataract surgery in the adult population of greater Beijing: the Beijing Eye Study. , 2011, Ophthalmology.
[29] D. Reich,et al. Principal components analysis corrects for stratification in genome-wide association studies , 2006, Nature Genetics.
[30] M. Daly,et al. Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions , 2009, PLoS genetics.
[31] C Kupfer,et al. Bowman lecture. The conquest of cataract: a global challenge. , 1985, Transactions of the ophthalmological societies of the United Kingdom.
[32] P. Mitchell,et al. Methodology of the Singapore Indian Chinese Cohort (SICC) Eye Study: Quantifying ethnic variations in the epidemiology of eye diseases in Asians , 2009, Ophthalmic epidemiology.
[33] Data production leads,et al. An integrated encyclopedia of DNA elements in the human genome , 2012 .
[34] Jost B Jonas,et al. Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations. , 2012, Human molecular genetics.
[35] Raymond K. Auerbach,et al. An Integrated Encyclopedia of DNA Elements in the Human Genome , 2012, Nature.
[36] Johnny S. H. Kwan,et al. GATES: a rapid and powerful gene-based association test using extended Simes procedure. , 2011, American journal of human genetics.
[37] P. Mitchell,et al. Smoking, socioeconomic factors, and age-related cataract: The Singapore Malay Eye study. , 2010, Archives of ophthalmology.
[38] Ayellet V. Segrè,et al. Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits , 2010, PLoS genetics.
[39] M. C. Leske,et al. The Lens Opacities Classification System III , 1993 .
[40] Kenny Q. Ye,et al. An integrated map of genetic variation from 1,092 human genomes , 2012, Nature.
[41] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[42] M. Owen,et al. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3) , 2000, Human Genetics.
[43] ENCODEConsortium,et al. An Integrated Encyclopedia of DNA Elements in the Human Genome , 2012, Nature.
[44] A. Morris,et al. Transethnic Meta-Analysis of Genomewide Association Studies , 2011, Genetic epidemiology.
[45] Yi Lu,et al. Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract , 2011, Molecular vision.
[46] S. Bhattacharya,et al. A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q , 2011, European Journal of Human Genetics.
[47] Karl W Broman,et al. Nuclear cataract shows significant familial aggregation in an older population after adjustment for possible shared environmental factors. , 2004, Investigative ophthalmology & visual science.
[48] Xu Ma,et al. A R54L Mutation of CRYAA Associated with Autosomal Dominant Nuclear Cataracts in a Chinese Family , 2013, Current eye research.
[49] T. Spector,et al. Genetic and environmental factors in age-related nuclear cataracts in monozygotic and dizygotic twins. , 2000, The New England journal of medicine.
[50] M. Frydman,et al. A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family. , 2000, Investigative ophthalmology & visual science.
[51] Liang Xu,et al. The Beijing Eye Study , 2009, Acta ophthalmologica.
[52] Xiaoping Zhou,et al. Genetic Variants on Chromosome 1q41 Influence Ocular Axial Length and High Myopia , 2012, PLoS genetics.
[53] J. Marchini,et al. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing , 2012, Nature Genetics.
[54] T. Wong,et al. The epidemiology of age related eye diseases in Asia , 2006, British Journal of Ophthalmology.
[55] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[56] F. Lee,et al. Population-based study on prevalence and risk factors of age-related cataracts in Peitou, Taiwan. , 2000, Zhonghua yi xue za zhi = Chinese medical journal; Free China ed.
[57] Jialiang Li,et al. Cataract Prevalence Varies Substantially with Assessment Systems: Comparison of Clinical and Photographic Grading in a Population-Based Study , 2011, Ophthalmic epidemiology.
[58] H. Bazan,et al. Phosphatidylinositol 3-kinase in bovine lens and its stimulation by insulin and IGF-1. , 2000, Investigative ophthalmology & visual science.
[59] Jialiang Zhao,et al. A recurrent mutation in CRYBA1 is associated with an autosomal dominant congenital nuclear cataract disease in a Chinese family , 2011, Molecular vision.
[60] C. Kupfer,et al. The conquest of cataract: a global challenge , 1985 .
[61] Manolis Kellis,et al. HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants , 2011, Nucleic Acids Res..