Common vs. rare allele hypotheses for complex diseases
Top Cited Papers
- 28 May 2009
- journal article
- review article
- Published by Elsevier
- Vol. 19 (3) , 212-219
- https://doi.org/10.1016/j.gde.2009.04.010
Abstract
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This publication has 47 references indexed in Scilit:
- Somatic mutations affect key pathways in lung adenocarcinomaNature, 2008
- Comprehensive genomic characterization defines human glioblastoma genes and core pathwaysNature, 2008
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence DataPublished by Elsevier ,2008
- The complete genome of an individual by massively parallel DNA sequencingNature, 2008
- Shifting Paradigm of Association Studies: Value of Rare Single-Nucleotide PolymorphismsAmerican Journal of Human Genetics, 2008
- A second generation human haplotype map of over 3.1 million SNPsNature, 2007
- Replicating genotype–phenotype associationsNature, 2007
- Completing the map of human genetic variationNature, 2007
- Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDLNature Genetics, 2007
- Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndromeNature Genetics, 1995