Common Disease-Common Variant Hypothesis
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-91280-6_1998
Reference8 articles.
1. Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., et al. (2010). A genome-wide scan for common alleles affecting risk for Autism. Human Molecular Genetics, 19(20), 4072–4082.
2. Borch-Johnsen, K., Burtt, N. P., Chen, H., Chines, P. S., Daly, M. J., Deodhar, P., Ding, C. J., et al. (2008). Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nature Genetics, 40(5), 638.
3. Chakravarti, A. (1999). Population genetics-making sense out of sequence. Nature genetics, 21(Suppl. 1), 56.
4. El-Fishawy, P., & State, M. W. (2010). The genetics of autism: Key issues, recent findings, and clinical implications. Psychiatric Clinics of North America, 33(1), 83–105.
5. Iyengar, S. K., & Elston, R. C. (2007). The genetic basis of complex traits: Rare variants or “common gene, common disease”. Methods in Molecular Biology, 376, 71. (Clifton, NJ).
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