Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
- Authors
- Zhong, Hua; Prentice, Ross L
- Year
- 2010
- Journal
- Genetic epidemiology
- PMID
- 19639606
- DOI
- 10.1002/gepi.20437
- PMCID
- PMC2796696
Genome-wide association studies (GWAS) provide an important approach for identifying common genetic variants that predispose to human disease. However, odds ratio (OR) estimates for the reported findings from GWAS discovery data are typically affected by a bias away from the null sometimes referred to the "winner's curse". Also standard confidence intervals (CIs) may have far from the desired coverage rates. We applied a bias reduction method to GWAS findings from several major complex human diseases, including breast cancer, colorectal cancer, lung cancer, prostate cancer, type I diabetes, and type II diabetes. We found the simple bias correction procedure allows one to estimate bias-adjusted ORs that have substantial consistency with ORs from subsequent replication studies, and that corresponding selection-adjusted CIs appear to help quantify the uncertainty of the findings. Selection-adjusted ORs and CIs can provide a reliable summary of GWAS data, and can help to choose single nucleotide polymorphisms for subsequent validation studies.
No figures extracted from this document.
No entities extracted from this document yet.
No uploaded files.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Potential Risk Factors and Therapeutic Targets for Dilated Cardiomyopathy Identified Through Mendelian Randomization Analysis. | Wang H et al. | β | 2026 | β |
| Correcting for volunteer bias in GWAS increases SNP effect sizes and heritability estimates. | van Alten S et al. | β | 2025 | β |
| Whole exome sequencing identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer in Hispanic/Latina women. | Nierenberg JL et al. | β | 2025 | β |
| Heterogeneity in precision oncology. | Tomasik B et al. | β | 2024 | β |
| An empirical investigation into the impact of winner's curse on estimates from Mendelian randomization. | Jiang T et al. | β | 2023 | β |
| The hidden factor: accounting for covariate effects in power and sample size computation for a binary trait. | Zhang Z et al. | β | 2023 | β |
| Accurate modeling of replication rates in genome-wide association studies by accounting for Winner's Curse and study-specific heterogeneity. | Zou J et al. | β | 2022 | β |
| An empirical investigation into the impact of winnerβs curse on estimates from Mendelian randomization | Jiang T et al. | β | 2022 | β |
| Common and rare variant associations with clonal haematopoiesis phenotypes. | Kessler MD et al. | β | 2022 | β |
| A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility. | Emami NC et al. | β | 2021 | β |
| Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. | Hu Y et al. | β | 2021 | β |
| Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction. | Conti DV et al. | β | 2021 | β |
| Elevated rates of autism, other neurodevelopmental and psychiatric diagnoses, and autistic traits in transgender and gender-diverse individuals. | Warrier V et al. | β | 2020 | β |
| Establishing a valid approach for estimating familial risk of cancer explained by common genetic variants. | Weigl K et al. | β | 2020 | β |
| Efficient estimation of disease odds ratios for follow-up genetic association studies. | Hu J et al. | β | 2019 | β |
| Genetic markers associated with long-term cardiovascular outcome in kidney transplant recipients. | PihlstrΓΈm HK et al. | β | 2019 | β |
| Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of Latinos. | Dunn EC et al. | β | 2018 | β |
| Genome-Wide Association Study of Heavy Smoking and Daily/Nondaily Smoking in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). | Saccone NL et al. | β | 2018 | β |
| Plasma levels of hsa-miR-152-3p are associated with diabetic nephropathy in patients with type 2 diabetes. | Roux M et al. | β | 2018 | β |
| Gene-environment interaction study for BMI reveals interactions between genetic factors and physical activity, alcohol consumption and socioeconomic status. | Rask-Andersen M et al. | β | 2017 | β |
| Genome-wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos. | Dunn EC et al. | β | 2017 | β |
| Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies. | Palmer C et al. | β | 2017 | β |
| Transplant genetics and genomics. | Yang JY et al. | β | 2017 | β |
| A model to determine colorectal cancer risk using common genetic susceptibility loci. | Hsu L et al. | β | 2015 | β |
| Polymorphisms influencing prostate-specific antigen concentration may bias genome-wide association studies on prostate cancer. | Dluzniewski PJ et al. | β | 2015 | β |
| Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event. | Poirier JG et al. | β | 2015 | β |
| A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort. | Nag A et al. | β | 2014 | β |
| ATP5H/KCTD2 locus is associated with Alzheimer's disease risk. | Boada M et al. | β | 2014 | β |
| Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus. | Oei L et al. | β | 2014 | β |
| Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology. | Li A et al. | β | 2014 | β |
| Multiple hypothesis testing in genomics. | Goeman JJ et al. | β | 2014 | β |
| The common variant rs4444235 near BMP4 confers genetic susceptibility of colorectal cancer: an updated meta-analysis based on a comprehensive statistical strategy. | Liu L et al. | β | 2014 | β |
| The SNP rs1883832 in CD40 gene and risk of atherosclerosis in Chinese population: a meta-analysis. | Yun Y et al. | β | 2014 | β |
| A genome-wide association study of a coronary artery disease risk variant. | Lee JY et al. | β | 2013 | β |
| Arsenic metabolism efficiency has a causal role in arsenic toxicity: Mendelian randomization and gene-environment interaction. | Pierce BL et al. | β | 2013 | β |
| Empirical Bayes correction for the Winner's Curse in genetic association studies. | Ferguson JP et al. | β | 2013 | β |
| Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. | Jeff JM et al. | β | 2013 | β |
| Genome-wide association study of the five-factor model of personality in young Korean women. | Kim HN et al. | β | 2013 | β |
| Replication study in Chinese population and meta-analysis supports association of the 5p15.33 locus with lung cancer. | Ke J et al. | β | 2013 | β |
| Strategies for developing prediction models from genome-wide association studies. | Wu J et al. | β | 2013 | β |
| The SNP rs402710 in 5p15.33 is associated with lung cancer risk: a replication study in Chinese population and a meta-analysis. | Lu X et al. | β | 2013 | β |
| This special issue contains several papers on clinical trials, exemplifying Ross Prentice's influence. Preface. | Cai J et al. | β | 2013 | β |
| A common polymorphism near the ESR1 gene is associated with risk of breast cancer: evidence from a case-control study and a meta-analysis. | Guo H et al. | β | 2012 | β |
| Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations. | Liu DJ et al. | β | 2012 | β |
| Fast computation for genome-wide association studies using boosted one-step statistics. | Voorman A et al. | β | 2012 | β |
| Fine mapping of 14q24.1 breast cancer susceptibility locus. | Lee P et al. | β | 2012 | β |
| Rare and common variants: twenty arguments. | Gibson G | β | 2012 | β |
| Replication study in Chinese population and meta-analysis supports association of the 11q23 locus with colorectal cancer. | Zou L et al. | β | 2012 | β |
| The SNP rs961253 in 20p12.3 is associated with colorectal cancer risk: a case-control study and a meta-analysis of the published literature. | Zheng X et al. | β | 2012 | β |
| What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations. | Panagiotou OA et al. | β | 2012 | β |
| A flexible genome-wide bootstrap method that accounts for ranking and threshold-selection bias in GWAS interpretation and replication study design. | Faye LL et al. | β | 2011 | β |
| BR-squared: a practical solution to the winner's curse in genome-wide scans. | Sun L et al. | β | 2011 | β |
| Discriminatory accuracy and potential clinical utility of genomic profiling for breast cancer risk in BRCA-negative women. | Comen E et al. | β | 2011 | β |
| Empirical evaluation of gene and environment interactions: methods and potential. | Prentice RL | β | 2011 | β |
| Genetic association of complement receptor 1 polymorphism rs3818361 in Alzheimer's disease. | AntΓΊnez C et al. | β | 2011 | β |
| Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. | Wijsman EM et al. | β | 2011 | β |
| The effect of survival bias on case-control genetic association studies of highly lethal diseases. | Anderson CD et al. | β | 2011 | β |
| The meta-analysis of genome-wide association studies. | Thompson JR et al. | β | 2011 | β |
| Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour. | Peden JF et al. | β | 2011 | β |
| Tweedie's Formula and Selection Bias. | Efron B | β | 2011 | β |
| A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. | Verweij KJ et al. | β | 2010 | β |
| A genome-wide scan for common alleles affecting risk for autism. | Anney R et al. | β | 2010 | β |
| Disease-associated alleles in genome-wide association studies are enriched for derived low frequency alleles relative to HapMap and neutral expectations. | Lachance J | β | 2010 | β |
| Estimation of effect size distribution from genome-wide association studies and implications for future discoveries. | Park JH et al. | β | 2010 | β |
| Eyes wide open: the personal genome project, citizen science and veracity in informed consent. | Angrist M | β | 2009 | β |