Regression-based association analysis with clustered haplotypes through use of genotypes.
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Chuhsing Kate Hsiao | Jung-Ying Tzeng | Jau-Tsuen Kao | J. Tzeng | C. K. Hsiao | J. Kao | Chih-Hao Wang | Chih-Hao Wang | Jung‐Ying Tzeng | Jung-Ying Tzeng
[1] T. Meerman,et al. Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspring , 1997 .
[2] P. Cullen. Evidence that triglycerides are an independent coronary heart disease risk factor. , 2000, The American journal of cardiology.
[3] T. Louis. Finding the Observed Information Matrix When Using the EM Algorithm , 1982 .
[4] P. Sham,et al. The future of association studies: gene-based analysis and replication. , 2004, American journal of human genetics.
[5] D. Schaid. Evaluating associations of haplotypes with traits , 2004, Genetic epidemiology.
[6] K. Crandall,et al. Empirical tests of some predictions from coalescent theory with applications to intraspecific phylogeny reconstruction. , 1993, Genetics.
[7] Daniel O. Stram,et al. Modeling and E-M Estimation of Haplotype-Specific Relative Risks from Genotype Data for a Case-Control Study of Unrelated Individuals , 2003, Human Heredity.
[8] K. Alberti,et al. Variable effects of the APOC3 –482C > T variant on insulin, glucose and triglyceride concentrations in different ethnic groups , 2001, Diabetologia.
[9] S. Humphries,et al. Associations of genotypes at the apolipoprotein AI‐CIII‐AIV, apolipoprotein B and lipoprotein lipase gene loci with coronary atherosclerosis and high density lipoprotein subclasses , 1994, Clinical genetics.
[10] E. Génin,et al. Use of closely related affected individuals for the genetic study of complex diseases in founder populations. , 2001, American journal of human genetics.
[11] P. Sham. Statistics in human genetics , 1997 .
[12] Jason Cooper,et al. Use of unphased multilocus genotype data in indirect association studies , 2004, Genetic epidemiology.
[13] Lue Ping Zhao,et al. A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies. , 2003, American journal of human genetics.
[14] N. Laird,et al. Estimation and Tests of Haplotype-Environment Interaction when Linkage Phase Is Ambiguous , 2003, Human Heredity.
[15] M. Slatkin,et al. Estimating the age of alleles by use of intraallelic variability. , 1997, American journal of human genetics.
[16] Peter H. Westfall,et al. Testing Association of Statistically Inferred Haplotypes with Discrete and Continuous Traits in Samples of Unrelated Individuals , 2002, Human Heredity.
[17] Jonathan C. Cohen,et al. An Apolipoprotein Influencing Triglycerides in Humans and Mice Revealed by Comparative Sequencing , 2001, Science.
[18] L. Wasserman,et al. On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. , 2003, American journal of human genetics.
[19] Larry Wasserman,et al. Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching , 2003 .
[20] Juliet M Chapman,et al. Detecting Disease Associations due to Linkage Disequilibrium Using Haplotype Tags: A Class of Tests and the Determinants of Statistical Power , 2003, Human Heredity.
[21] D. Lin,et al. Haplotype‐based association analysis in cohort studies of unrelated individuals , 2004, Genetic epidemiology.
[22] D. Zeng,et al. Estimating haplotype‐disease associations with pooled genotype data , 2005, Genetic epidemiology.
[23] M. McPeek,et al. Assessment of linkage disequilibrium by the decay of haplotype sharing, with application to fine-scale genetic mapping. , 1999, American journal of human genetics.
[24] E. Génin,et al. Search for multifactorial disease susceptibility genes in founder populations , 2000, Annals of human genetics.
[25] P. Marjoram,et al. Fine-scale mapping of disease genes with multiple mutations via spatial clustering techniques. , 2003, American journal of human genetics.
[26] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[27] D. Boos. On Generalized Score Tests , 1992 .
[28] J. Kent. Robust properties of likelihood ratio tests , 1982 .
[29] Andrew P Morris,et al. Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes. , 2004, American journal of human genetics.
[30] Leena Peltonen,et al. Dissecting Human Disease in the Postgenomic Era , 2001, Science.
[31] Jung-Ying Tzeng,et al. Evolutionary‐based grouping of haplotypes in association analysis , 2005, Genetic epidemiology.
[32] K. Roeder,et al. Evolutionary‐based association analysis using haplotype data , 2003 .
[33] J. Wall,et al. Assessing the performance of the haplotype block model of linkage disequilibrium. , 2003, American journal of human genetics.
[34] P. Talmud,et al. Contribution of Apolipoprotein C-III Gene Variants to Determination of Triglyceride Levels and Interaction With Smoking in Middle-Aged Men , 2000, Arteriosclerosis, thrombosis, and vascular biology.
[35] E. Lander,et al. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease , 2003, Nature Genetics.
[36] K. Chien,et al. A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia. , 2003, Human molecular genetics.
[37] C Charles Gu,et al. Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes , 2004, Genetic epidemiology.
[38] J. Buring,et al. Fasting triglycerides, high-density lipoprotein, and risk of myocardial infarction. , 1997, Circulation.
[39] M. Daly,et al. High-resolution haplotype structure in the human genome , 2001, Nature Genetics.
[40] H. Hein,et al. Triglyceride concentration and ischemic heart disease: an eight-year follow-up in the Copenhagen Male Study. , 1998, Circulation.
[41] C. E. SHANNON,et al. A mathematical theory of communication , 1948, MOCO.
[42] Frank Dudbridge,et al. Haplotype tagging for the identification of common disease genes , 2001, Nature Genetics.
[43] D. Schaid,et al. Score tests for association between traits and haplotypes when linkage phase is ambiguous. , 2002, American journal of human genetics.
[44] A. von Eckardstein,et al. Hypertriglyceridemia and elevated lipoprotein(a) are risk factors for major coronary events in middle-aged men. , 1996, The American journal of cardiology.
[45] P. Wilson,et al. Restriction fragment length polymorphisms of the apolipoprotein A-I, C-III, A-IV gene locus. Relationships with lipids, apolipoproteins, and premature coronary artery disease. , 1991, Atherosclerosis.
[46] Francis S. Collins,et al. Variations on a Theme: Cataloging Human DNA Sequence Variation , 1997, Science.
[47] Richard R. Hudson,et al. Generating samples under a Wright-Fisher neutral model of genetic variation , 2002, Bioinform..
[48] E. Génin,et al. Missing data in haplotype analysis: a study on the MILC method. , 2002 .
[49] J. Stephens,et al. Haplotype Variation and Linkage Disequilibrium in 313 Human Genes , 2001, Science.
[50] G. Satten,et al. Inference on haplotype effects in case-control studies using unphased genotype data. , 2003, American journal of human genetics.
[51] G. Satten,et al. Comparison of prospective and retrospective methods for haplotype inference in case‐control studies , 2004, Genetic epidemiology.
[52] John Molitor,et al. Application of Bayesian spatial statistical methods to analysis of haplotypes effects and gene mapping , 2003, Genetic epidemiology.
[53] K. Roeder,et al. Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes. , 2001, American journal of human genetics.
[54] Kathryn Roeder,et al. Analysis of single‐locus tests to detect gene/disease associations , 2005, Genetic epidemiology.
[55] Alessandro Rinaldo,et al. Characterization of multilocus linkage disequilibrium , 2005, Genetic epidemiology.