Combined genotype and haplotype tests for region-based association studies
暂无分享,去创建一个
T. Wong | A. Thalamuthu | T. Aung | C. Khor | E. Vithana | A. Salim | Sergii Zakharov | T. Wong | T. Wong | T. Wong
[1] A. Thalamuthu,et al. Combined genotype and haplotype tests for region-based association studies , 2013, BMC Genomics.
[2] P. Bosco,et al. Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease (Molecular Psychiatry (2013) 18 (521) DOI: 10.1038/mp.2012.75)) , 2013 .
[3] Lei Sun,et al. Robust and Powerful Tests for Rare Variants Using Fisher's Method to Combine Evidence of Association From Two or More Complementary Tests , 2013, Genetic epidemiology.
[4] M Mancuso,et al. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease , 2012, Molecular Psychiatry.
[5] E. Ingelsson,et al. Genome‐wide and gene‐based association implicates FRMD6 in alzheimer disease , 2012, Human mutation.
[6] Jost B Jonas,et al. Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations. , 2012, Human molecular genetics.
[7] Antonio J. Berlanga-Taylor,et al. Rare variants in the CYP27B1 gene are associated with multiple sclerosis , 2011, Annals of neurology.
[8] Qing Lu,et al. An aggregating U-Test for a genetic association study of quantitative traits , 2011, BMC proceedings.
[9] A. Thalamuthu,et al. Association tests for rare and common variants based on genotypic and phenotypic measures of similarity between individuals , 2011, BMC proceedings.
[10] K. Cosgrove,et al. Rare Nonsynonymous Variants in Alpha-4 Nicotinic Acetylcholine Receptor Gene Protect Against Nicotine Dependence , 2011, Biological Psychiatry.
[11] Xu Shi. Rare-variant association testing for sequencing data with the sequence kernel association test. , 2011, American journal of human genetics.
[12] Xihong Lin,et al. Rare-variant association testing for sequencing data with the sequence kernel association test. , 2011, American journal of human genetics.
[13] G. Kirov,et al. DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls , 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[14] M. Rieder,et al. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. , 2011, American journal of human genetics.
[15] Kathryn Roeder,et al. Testing for an Unusual Distribution of Rare Variants , 2011, PLoS genetics.
[16] Tin Aung,et al. Collagen-related genes influence the glaucoma risk factor, central corneal thickness. , 2011, Human molecular genetics.
[17] Iuliana Ionita-Laza,et al. A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease , 2011, PLoS genetics.
[18] Anbupalam Thalamuthu,et al. Pathway-based analysis using reduced gene subsets in genome-wide association studies , 2011, BMC Bioinformatics.
[19] Yun Li,et al. To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests. , 2010, American journal of human genetics.
[20] V. Bansal,et al. Statistical analysis strategies for association studies involving rare variants , 2010, Nature Reviews Genetics.
[21] Paul J. Rathouz,et al. An Evolutionary Framework for Association Testing in Resequencing Studies , 2010, PLoS genetics.
[22] Wensheng Zhu,et al. Genome‐wide association studies using haplotype clustering with a new haplotype similarity , 2010, Genetic epidemiology.
[23] M. Schatz,et al. Assembly of large genomes using second-generation sequencing. , 2010, Genome research.
[24] S. Piaserico,et al. PTCH1 gene haplotype association with basal cell carcinoma after transplantation , 2010, The British journal of dermatology.
[25] Deanne M. Taylor,et al. Powerful SNP-set analysis for case-control genome-wide association studies. , 2010, American journal of human genetics.
[26] P. Dieudé,et al. Phenotype-Haplotype Correlation of IRF5 in Systemic Sclerosis: Role of 2 Haplotypes in Disease Severity , 2010, The Journal of Rheumatology.
[27] H. Lemij,et al. Foveal cone photoreceptor involvement in primary open-angle glaucoma , 2010, Graefe's Archive for Clinical and Experimental Ophthalmology.
[28] R. Elston,et al. Detecting rare variants for complex traits using family and unrelated data , 2010, Genetic epidemiology.
[29] 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.
[30] Ryan D. Hernandez,et al. Inferring the Joint Demographic History of Multiple Populations from Multidimensional SNP Frequency Data , 2009, PLoS genetics.
[31] Patrick Wincker,et al. Generation and analysis of a 29,745 unique Expressed Sequence Tags from the Pacific oyster (Crassostrea gigas) assembled into a publicly accessible database: the GigasDatabase , 2009, BMC Genomics.
[32] P. Donnelly,et al. A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies , 2009, PLoS genetics.
[33] Wei Guo,et al. Generalized linear modeling with regularization for detecting common disease rare haplotype association , 2009, Genetic epidemiology.
[34] Liang Xu,et al. The Beijing Eye Study , 2009, Acta ophthalmologica.
[35] T. Wong,et al. Central corneal thickness and its associations with ocular and systemic factors: the Singapore Malay Eye Study. , 2009, American journal of ophthalmology.
[36] Benjamin J. Wright,et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease , 2009, Nature Genetics.
[37] William Wheeler,et al. Genome-Wide and Candidate Gene Association Study of Cigarette Smoking Behaviors , 2009, PloS one.
[38] S. Browning,et al. A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic , 2009, PLoS genetics.
[39] Vineet Bafna,et al. HapCUT: an efficient and accurate algorithm for the haplotype assembly problem , 2008, ECCB.
[40] Tien Yin Wong,et al. Prevalence and causes of low vision and blindness in an urban malay population: the Singapore Malay Eye Study. , 2008, Archives of ophthalmology.
[41] A. Halpern,et al. An MCMC algorithm for haplotype assembly from whole-genome sequence data. , 2008, Genome research.
[42] Ryan D. Hernandez,et al. Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome , 2008, PLoS genetics.
[43] J. Jonas,et al. Central corneal thickness in adult Chinese. Association with ocular and general parameters. The Beijing Eye Study , 2008, Graefe's Archive for Clinical and Experimental Ophthalmology.
[44] Gary O Zerbe,et al. Permutation‐based adjustments for the significance of partial regression coefficients in microarray data analysis , 2008, Genetic epidemiology.
[45] B. Browning,et al. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. , 2007, American journal of human genetics.
[46] Yu-mei Li,et al. An Entropy-Based Measure for QTL Mapping Using Extreme Samples of Population , 2007, Human Heredity.
[47] David V Conti,et al. Testing association between disease and multiple SNPs in a candidate gene , 2007, Genetic epidemiology.
[48] 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.
[49] D. Reich,et al. Principal components analysis corrects for stratification in genome-wide association studies , 2006, Nature Genetics.
[50] D. Schaid. Power and Sample Size for Testing Associations of Haplotypes with Complex Traits , 2006, Annals of human genetics.
[51] Qiuying Sha,et al. Tests of Association Between Quantitative Traits and Haplotypes In A Reduced‐Dimensional Space , 2005, Annals of human genetics.
[52] Peter H. Westfall,et al. Testing Association of Statistically Inferred Haplotypes with Discrete and Continuous Traits in Samples of Unrelated Individuals , 2002, Human Heredity.
[53] P. Donnelly,et al. A new statistical method for haplotype reconstruction from population data. , 2001, American journal of human genetics.
[54] M. Xiong,et al. Haplotypes vs single marker linkage disequilibrium tests: what do we gain? , 2001, European Journal of Human Genetics.
[55] Pierre Legendre,et al. An empirical comparison of permutation methods for tests of partial regression coefficients in a linear model , 1999 .
[56] David A. Freedman,et al. A Nonstochastic Interpretation of Reported Significance Levels , 1983 .
[57] Shamil R Sunyaev,et al. Pooled association tests for rare variants in exon-resequencing studies. , 2010, American journal of human genetics.
[58] Peter E. Kennedy. Randomization Tests in Econometrics , 1995 .
[59] C. Braak,et al. Permutation Versus Bootstrap Significance Tests in Multiple Regression and Anova , 1992 .
[60] S. Stouffer. Adjustment during army life , 1977 .