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CPS2057 Ana C. M. Ciconelle et al.
References
1. 1000 Genomes Project Consortium (2016). HHS Public Access. Nature
526(7571): 68–74.
2. Affymetrix (2017). Affymetrix Power Tools: MANUAL: apt-
probesetsummarize (1.20.0).
3. Boomsma et al. (2014). The Genome of the Netherlands: Design, and
project goals. European Journal of Human Genetics 22(2):221–227.
4. Egan et al. (2016). Cohort profile: the Baependi Heart Study—a family-
based, highly admixed cohort study in a rural Brazilian town. BMJ Open
6(10):e011598.
5. Lewis C. M., Knight J. (2012). Introduction to genetic association studies.
Cold Spring Harbor Protocols 2012(3):297–306.
6. Manolio T. A. et al. (2010). Finding the missing heritability of complex
diseases. Nature 461(7265):747–753.
7. The International HapMap Consortium (2003). The International HapMap
Project. Nature 426:789– 796.
8. Sanna et al. (2011). Fine Mapping of Five Loci Associated with Low-
Density Lipoprotein Cholesterol Detects Variants That Double the
Explained Heritability. PLoS Genetics 7(7).
9. Scharpf R. B. et al. (2014). Copy number polymorphisms near SLC2A9 are
associated with serum uric acid concentrations. BMC Genetics 15(1):1–13.
10. Wang et al.(2007). PennCNV: An integrated hidden Markov model
designed for high-resolution copy number variation detection in whole-
genome SNP genotyping data. Genome Research 17(11):1665–1674.

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