Estimating Missing Heritability for Disease from Genome-wide Association Studies
Top Cited Papers
- 1 March 2011
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 88 (3) , 294-305
- https://doi.org/10.1016/j.ajhg.2011.02.002
Abstract
No abstract availableFunding Information
- National Health and Medical Research Council (389892, 442915, 496688, 613601, 613672)
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (480-05-003)
- Australian Research Council (DP0770096, DP1093900)
- Wellcome Trust (076113)
This publication has 28 references indexed in Scilit:
- GCTA: A Tool for Genome-wide Complex Trait AnalysisAmerican Journal of Human Genetics, 2011
- A simple and fast two‐locus quality control test to detect false positives due to batch effects in genome‐wide association studiesGenetic Epidemiology, 2010
- Genomewide Association Studies and Assessment of the Risk of DiseaseNew England Journal of Medicine, 2010
- Common SNPs explain a large proportion of the heritability for human heightNature Genetics, 2010
- The Genetic Interpretation of Area under the ROC Curve in Genomic ProfilingPLoS Genetics, 2010
- Finding the missing heritability of complex diseasesNature, 2009
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based studyThe Lancet, 2009
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseNature Genetics, 2008
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsNature, 2007
- Principal components analysis corrects for stratification in genome-wide association studiesNature Genetics, 2006