Enriched power of disease-concordant twin-case-only design in detecting interactions in genome-wide association studies
Author:
Funder
Lundbeckfonden
Sundhed og Sygdom, Det Frie Forskningsråd
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/s41431-018-0320-2.pdf
Reference22 articles.
1. Visscher PM, Wray NR, Zhang Q, et al. 10 years of GWAS discovery: biology, function, and translation. Am J Hum Genet. 2017;101:5–22.
2. Stranger BE, Stahl EA, Raj T. Progress and promise of genome-wide association studies for human complex trait genetics. Genetics. 2011;187:367–83.
3. Price AL, Spencer CCA, Donnelly P. Progress and promise in understanding the genetic basis of common diseases. Proc R Soc B. 2015;282:20151684.
4. Onay VÜ, Briollais L, Knight JA, et al. SNP-SNP interactions in breast cancer susceptibility. BMC Cancer. 2006;6:1–16.
5. Dinu I, Mahasirimongkol S, Liu Q, et al. SNP-SNP interactions discovered by logic regression explain Crohn’s disease genetics. PLoS ONE. 2012;7:e43035.
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