Multivariate Association Test Using Haplotype Trend Regression
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Lei Zhang | Hong-Wen Deng | Yu-Fang Pei | H. Deng | Jianfeng Liu | Lei Zhang | Yu-Fang Pei | Jianfeng Liu
[1] Qihua Tan,et al. Haplotype association analysis of human disease traits using genotype data of unrelated individuals. , 2005, Genetical research.
[2] L. Almasy,et al. A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. , 2002, American journal of human genetics.
[3] Mark Daly,et al. Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..
[4] Sharon R Browning,et al. Multilocus association mapping using variable-length Markov chains. , 2006, American journal of human genetics.
[5] J. Blangero,et al. Genetic and environmental contributions to cardiovascular risk factors in Mexican Americans. The San Antonio Family Heart Study. , 1996, Circulation.
[6] M. McCarthy,et al. Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes. , 2002, American journal of human genetics.
[7] H. Deng,et al. Bivariate association analyses for the mixture of continuous and binary traits with the use of extended generalized estimating equations , 2009, Genetic epidemiology.
[8] R. Recker,et al. Polymorphisms of estrogen-biosynthesis genes CYP17 and CYP19 may influence age at menarche: a genetic association study in Caucasian females. , 2006, Human molecular genetics.
[9] D. Balding,et al. Fine mapping of disease genes via haplotype clustering , 2006, Genetic epidemiology.
[10] Christoph Lange,et al. A multivariate family-based association test using generalized estimating equations: FBAT-GEE. , 2003, Biostatistics.
[11] Paul Scheet,et al. A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. , 2006, American journal of human genetics.
[12] Wing-Kin Sung,et al. Association mapping via regularized regression analysis of single-nucleotide-polymorphism haplotypes in variable-sized sliding windows. , 2007, American journal of human genetics.
[13] Peter H. Westfall,et al. Testing Association of Statistically Inferred Haplotypes with Discrete and Continuous Traits in Samples of Unrelated Individuals , 2002, Human Heredity.
[14] Mariza de Andrade,et al. Comparison of Multivariate Tests for Genetic Linkage , 2001, Human Heredity.
[15] J. Haines,et al. Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease. , 2001, JAMA.
[16] T. Meitinger,et al. ALOX5AP Gene and the PDE4D Gene in a Central European Population of Stroke Patients , 2005, Stroke.
[17] J. Bader. The relative power of SNPs and haplotype as genetic markers for association tests. , 2001, Pharmacogenomics.
[18] B. Browning,et al. Efficient multilocus association testing for whole genome association studies using localized haplotype clustering , 2007, Genetic epidemiology.
[19] N. Schork,et al. Generalized genomic distance-based regression methodology for multilocus association analysis. , 2006, American journal of human genetics.
[20] J. Beckmann,et al. A highly significant association between a COMT haplotype and schizophrenia. , 2002, American journal of human genetics.
[21] Philippe Froguel,et al. Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. , 2008, Human molecular genetics.
[22] Eleftheria Zeggini,et al. Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites. , 2004, American journal of human genetics.
[23] J Blangero,et al. Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials. , 1999, American journal of human genetics.
[24] Richard R. Hudson,et al. Generating samples under a Wright-Fisher neutral model of genetic variation , 2002, Bioinform..
[25] K. Clément,et al. GAD2 on Chromosome 10p12 Is a Candidate Gene for Human Obesity , 2003, PLoS biology.
[26] Simon E Fisher,et al. Use of multivariate linkage analysis for dissection of a complex cognitive trait. , 2003, American journal of human genetics.
[27] David M. Evans,et al. The power of multivariate quantitative-trait loci linkage analysis is influenced by the correlation between variables. , 2002, American journal of human genetics.
[28] Yun Li,et al. CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration , 2006, Nature Genetics.
[29] N. Schork,et al. Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease. , 2001, Genome research.
[30] S. Fisher,et al. Developmental dyslexia: genetic dissection of a complex cognitive trait , 2002, Nature Reviews Neuroscience.
[31] David L Duffy,et al. A Simulation Study Concerning the Effect of Varying the Residual Phenotypic Correlation on the Power of Bivariate Quantitative Trait Loci Linkage Analysis , 2004, Behavior genetics.
[32] S. Gray. Asthma genetics , 2001, Genome Biology.
[33] Fengzhu Sun,et al. Haplotype block structure and its applications to association studies: power and study designs. , 2002, American journal of human genetics.
[34] D. Balding. A tutorial on statistical methods for population association studies , 2006, Nature Reviews Genetics.