On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles

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Items 201–300 of 369

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12. G-T haplotype established by rs3785889-rs16941382 in GOSR2 gene is associated with coronary artery disease in Chinese Han population
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16. Fine mapping by linkage and association in nuclear family and case-control designs
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17. Robust estimation and testing of haplotype effects in case‐control studies
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18. Haplotype Reconstruction Error as a Classical Misclassification Problem: Introducing Sensitivity and Specificity as Error Measures
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20. Haplotypes of the inducible nitric oxide synthase gene are strongly associated with exhaled nitric oxide levels in adults: a population-based study
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21. Power of Genetic Association Studies in the Presence of Linkage Disequilibrium and Allelic Heterogeneity
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24. P-selectin gene genotypes or haplotypes and cardiovascular complications in type 2 diabetes mellitus
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32. Haplotype of smoothelin gene associated with essential hypertension
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34. Genetic Variation in the 3'-Untranslated Region of NBN Gene Is Associated with Gastric Cancer Risk in a Chinese Population
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36. A Unified Framework for Haplotype Inference in Nuclear Families
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37. Haplotype Misclassification Resulting from Statistical Reconstruction and Genotype Error, and Its Impact on Association Estimates
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38. Haplotyping using a combination of polymerase chain reaction–single-strand conformational polymorphism analysis and haplotype-specific PCR amplification
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40. Association of C5aR1genetic polymorphisms with coronary artery disease in a Han population in Xinjiang, China
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41. Association of KCNB1 polymorphisms with lipid metabolisms and insulin resistance: a case-control design of population-based cross-sectional study in Chinese Han population
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42. Cumulative risk and protection effect of serotonergic genes on male antisocial behaviour: results from a prospective cohort assessed in adolescence and early adulthood
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43. Statistically efficient association analysis of quantitative traits with haplotypes and untyped SNPs in family studies
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44. LPL, FNDC5 and PPARγ gene polymorphisms related to body composition parameters and lipid metabolic profile in adolescents from Southern Italy
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45. Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia
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46. Global transmission/disequilibrium tests based on haplotype sharing in multiple candidate genes
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47. Association between AUTS2 haplotypes and alcohol dependence in a Japanese population
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48. Haplotype-based, case–control study of the receptor (calcitonin) activity-modifying protein (RAMP) 1 gene in essential hypertension
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49. Bivariate logistic Bayesian LASSO for detecting rare haplotype association with two correlated phenotypes
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50. Age-dependent association of polymorphisms in the promoter and 5′-untranslated region of the norepinephrine transporter gene with generalized anxiety disorder
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51. Haplotype Association Analysis
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52. A haplotype inference algorithm for trios based on deterministic sampling
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53. Robust testing of haplotype/disease association
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56. Haplotype Reconstruction in Large Pedigrees with Untyped Individuals through IBD Inference
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57. A Statistical Model for Genetic Mapping of Viral Infection by Integrating Epidemiological Behavior
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58. Family-Based Multi-SNP X Chromosome Analysis Using Parent Information
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59. Association between genetic polymorphisms in the melatonin receptor type 1 A gene and sleep bruxism
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62. An EM algorithm based on an internal list for estimating haplotype distributions of rare variants from pooled genotype data
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63. Determination of haplotypes at structurally complex regions using emulsion haplotype fusion PCR
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64. A fast collapsed data method for estimating haplotype frequencies from pooled genotype data with applications to the study of rare variants
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