| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/GEPI.20162 |
| P8608 | Fatcat ID | release_ukj5ooprnzhhxdjejzxkkc63ga |
| P698 | PubMed publication ID | 16755536 |
| P50 | author | Bingshu E. Chen | Q56027887 |
| Philip S. Rosenberg | Q62109823 | ||
| Lori C Sakoda | Q89685276 | ||
| P2093 | author name string | Ann W Hsing | |
| P2860 | cites work | A New Statistical Method for Haplotype Reconstruction from Population Data | Q27860495 |
| Efficiency and power in genetic association studies | Q28278645 | ||
| Replication validity of genetic association studies | Q29615456 | ||
| Score tests for association between traits and haplotypes when linkage phase is ambiguous | Q29616281 | ||
| An improved Bonferroni procedure for multiple tests of significance | Q30050394 | ||
| Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease | Q30625643 | ||
| Commentary: meta-analysis of individual participants' data in genetic epidemiology | Q30707324 | ||
| Inference on haplotype effects in case-control studies using unphased genotype data | Q33195240 | ||
| Comparison of type I error for multiple test corrections in large single-nucleotide polymorphism studies using principal components versus haplotype blocking algorithms | Q33232831 | ||
| A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies | Q33904720 | ||
| A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other | Q33909759 | ||
| The future of association studies: gene-based analysis and replication | Q33910011 | ||
| Single nucleotide polymorphisms and the future of genetic epidemiology | Q34081504 | ||
| Estimating haplotype frequencies and standard errors for multiple single nucleotide polymorphisms | Q34269636 | ||
| SNP association studies in Alzheimer's disease highlight problems for complex disease analysis. | Q34288840 | ||
| Power calculations for genetic association studies using estimated probability distributions | Q37217339 | ||
| Rising incidence of biliary tract cancers in Shanghai, China | Q40870817 | ||
| Estimation and tests of haplotype-environment interaction when linkage phase is ambiguous | Q47724047 | ||
| Model-free analysis and permutation tests for allelic associations | Q52027186 | ||
| Haplotype tagging for the identification of common disease genes | Q59200321 | ||
| Tests for Linear Trends in Proportions and Frequencies | Q105198455 | ||
| P433 | issue | 6 | |
| P921 | main subject | multiple hypothesis testing | Q110783633 |
| P304 | page(s) | 495-507 | |
| P577 | publication date | 2006-09-01 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Resampling-based multiple hypothesis testing procedures for genetic case-control association studies | |
| P478 | volume | 30 |
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| Q33334257 | PGA: power calculator for case-control genetic association analyses. |
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