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Chao-Yu Guo, Ph.D.

Affiliations: 
2004 Boston University, Boston, MA, United States 
Area:
Biostatistics Biology, Genetics
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"Chao-Yu Guo"
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Parents

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Adrienne Cupples grad student 2004 Boston University
 (Extensions of family-based genetic tests of linkage and/or association for a dichotomous trait.)

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Publications

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Guo CY, Wang RH, Yang HC. (2021) Family-based gene-environment interaction using sequence kernel association test (FGE-SKAT) for complex quantitative traits. Scientific Reports. 11: 7431
Yang Q, Wu H, Guo CY, et al. (2010) Analyze multivariate phenotypes in genetic association studies by combining univariate association tests. Genetic Epidemiology. 34: 444-54
Chen MH, Larson MG, Hsu YH, et al. (2010) A three-stage approach for genome-wide association studies with family data for quantitative traits. Bmc Genetics. 11: 40
Murabito JM, Keyes MJ, Guo CY, et al. (2009) Cross-sectional relations of multiple inflammatory biomarkers to peripheral arterial disease: The Framingham Offspring Study. Atherosclerosis. 203: 509-14
Guo CY, Lunetta KL, DeStefano AL, et al. (2009) Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls. Genetic Epidemiology. 33: 54-62
Parikh NI, Hwang SJ, Yang Q, et al. (2008) Clinical correlates and heritability of cystatin C (from the Framingham Offspring Study). The American Journal of Cardiology. 102: 1194-8
Guo CY, Cupples LA, Yang Q. (2008) Testing informative missingness in genetic studies using case-parent triads. European Journal of Human Genetics : Ejhg. 16: 992-1001
Chen MH, Cui J, Guo CY, et al. (2007) Joint modeling of linkage and association using affected sib-pair data. Bmc Proceedings. 1: S38
Guo CY. (2007) The impact of complex informative missingness on the validity of the transmission/disequilibrium test (TDT). Bmc Proceedings. 1: S26
Newton-Cheh C, Guo CY, Wang TJ, et al. (2007) Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. Bmc Medical Genetics. 8: S7
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