Genome wide association study gateway—transitioning variants from association to causality in complex diseases
Author:
Affiliation:
1. Institute of Human Genetics, TUM School of Medicine and Health, Technical University of Munich , Munich , Germany
2. Neurogenetic Systems Analysis Group, Institute of Neurogenomics , Helmholtz Munich , Germany
Publisher
Oxford University Press (OUP)
Link
https://academic.oup.com/sleep/advance-article-pdf/doi/10.1093/sleep/zsae116/57987001/zsae116.pdf
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3. Annotation: the analysis of variance and the analysis of causes;Lewontin;Am J Hum Genet.,1974
4. Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease;Cooper;Hum Genet.,2013
5. Rare penetrant mutations confer severe risk of common diseases;Fiziev;Science.,2023
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