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Chao-Yu Guo, Ph.D. - Publications

Affiliations: 
2004 Boston University, Boston, MA, United States 
Area:
Biostatistics Biology, Genetics
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Guo CY, Wang RH, Yang HC. Family-based gene-environment interaction using sequence kernel association test (FGE-SKAT) for complex quantitative traits. Scientific Reports. 11: 7431. PMID 33795796 DOI: 10.1038/s41598-021-86871-2  0.302
2010 Yang Q, Wu H, Guo CY, Fox CS. Analyze multivariate phenotypes in genetic association studies by combining univariate association tests. Genetic Epidemiology. 34: 444-54. PMID 20583287 DOI: 10.1002/Gepi.20497  0.425
2010 Chen MH, Larson MG, Hsu YH, Peloso GM, Guo CY, Fox CS, Atwood LD, Yang Q. A three-stage approach for genome-wide association studies with family data for quantitative traits. Bmc Genetics. 11: 40. PMID 20470424 DOI: 10.1186/1471-2156-11-40  0.373
2009 Murabito JM, Keyes MJ, Guo CY, Keaney JF, Vasan RS, D'Agostino RB, Benjamin EJ. Cross-sectional relations of multiple inflammatory biomarkers to peripheral arterial disease: The Framingham Offspring Study. Atherosclerosis. 203: 509-14. PMID 18701106 DOI: 10.1016/J.Atherosclerosis.2008.06.031  0.338
2009 Guo CY, Lunetta KL, DeStefano AL, Cupples LA. Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls. Genetic Epidemiology. 33: 54-62. PMID 18636528 DOI: 10.1002/Gepi.20356  0.355
2008 Parikh NI, Hwang SJ, Yang Q, Larson MG, Guo CY, Robins SJ, Sutherland P, Benjamin EJ, Levy D, Fox CS. Clinical correlates and heritability of cystatin C (from the Framingham Offspring Study). The American Journal of Cardiology. 102: 1194-8. PMID 18940290 DOI: 10.1016/J.Amjcard.2008.06.039  0.347
2008 Guo CY, Cupples LA, Yang Q. Testing informative missingness in genetic studies using case-parent triads. European Journal of Human Genetics : Ejhg. 16: 992-1001. PMID 18337731 DOI: 10.1038/Ejhg.2008.38  0.332
2007 Chen MH, Cui J, Guo CY, Cupples LA, Van Eerdewegh P, Dupuis J, Yang Q. Joint modeling of linkage and association using affected sib-pair data. Bmc Proceedings. 1: S38. PMID 18466536 DOI: 10.1186/1753-6561-1-S1-S38  0.382
2007 Guo CY. The impact of complex informative missingness on the validity of the transmission/disequilibrium test (TDT). Bmc Proceedings. 1: S26. PMID 18466523 DOI: 10.1186/1753-6561-1-S1-S26  0.334
2007 Newton-Cheh C, Guo CY, Wang TJ, O'donnell CJ, Levy D, Larson MG. Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. Bmc Medical Genetics. 8: S7. PMID 17903306 DOI: 10.1186/1471-2350-8-S1-S7  0.346
2007 Larson MG, Atwood LD, Benjamin EJ, Cupples LA, D'Agostino RB, Fox CS, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Murabito JM, Newton-Cheh C, O'Donnell CJ, Seshadri S, Vasan RS, et al. Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. Bmc Medical Genetics. 8: S5. PMID 17903304 DOI: 10.1186/1471-2350-8-S1-S5  0.377
2007 Lunetta KL, D'Agostino RB, Karasik D, Benjamin EJ, Guo CY, Govindaraju R, Kiel DP, Kelly-Hayes M, Massaro JM, Pencina MJ, Seshadri S, Murabito JM. Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Bmc Medical Genetics. 8: S13. PMID 17903295 DOI: 10.1186/1471-2350-8-S1-S13  0.41
2007 Cupples LA, Arruda HT, Benjamin EJ, D'Agostino RB, Demissie S, DeStefano AL, Dupuis J, Falls KM, Fox CS, Gottlieb DJ, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Kathiresan S, et al. The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. Bmc Medical Genetics. 8: S1. PMID 17903291 DOI: 10.1186/1471-2350-8-S1-S1  0.651
2007 Newton-Cheh C, Guo CY, Larson MG, Musone SL, Surti A, Camargo AL, Drake JA, Benjamin EJ, Levy D, D'Agostino RB, Hirschhorn JN, O'donnell CJ. Common genetic variation in KCNH2 is associated with QT interval duration: the Framingham Heart Study. Circulation. 116: 1128-36. PMID 17709632 DOI: 10.1161/Circulationaha.107.710780  0.317
2007 Mitchell GF, Guo CY, Benjamin EJ, Larson MG, Keyes MJ, Vita JA, Vasan RS, Levy D. Cross-sectional correlates of increased aortic stiffness in the community: the Framingham Heart Study. Circulation. 115: 2628-36. PMID 17485578 DOI: 10.1161/Circulationaha.106.667733  0.312
2007 Mitchell GF, Guo CY, Kathiresan S, Vasan RS, Larson MG, Vita JA, Keyes MJ, Vyas M, Newton-Cheh C, Musone SL, Camargo AL, Drake JA, Levy D, O'Donnell CJ, Hirschhorn JN, et al. Vascular stiffness and genetic variation at the endothelial nitric oxide synthase locus: the Framingham Heart study. Hypertension. 49: 1285-90. PMID 17404185 DOI: 10.1161/Hypertensionaha.106.085266  0.352
2007 Newton-Cheh C, Guo CY, Gona P, Larson MG, Benjamin EJ, Wang TJ, Kathiresan S, O'Donnell CJ, Musone SL, Camargo AL, Drake JA, Levy D, Hirschhorn JN, Vasan RS. Clinical and genetic correlates of aldosterone-to-renin ratio and relations to blood pressure in a community sample. Hypertension. 49: 846-56. PMID 17296870 DOI: 10.1161/01.Hyp.0000258554.87444.91  0.367
2007 Guo CY, Lunetta KL, DeStefano AL, Ordovas JM, Cupples LA. Informative-transmission disequilibrium test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring. Genetic Epidemiology. 31: 115-33. PMID 17123304 DOI: 10.1002/Gepi.20195  0.367
2006 Murabito JM, Guo CY, Fox CS, D'Agostino RB. Heritability of the ankle-brachial index: the Framingham Offspring study. American Journal of Epidemiology. 164: 963-8. PMID 16928729 DOI: 10.1093/Aje/Kwj295  0.37
2006 Kathiresan S, Larson MG, Vasan RS, Guo CY, Gona P, Keaney JF, Wilson PW, Newton-Cheh C, Musone SL, Camargo AL, Drake JA, Levy D, O'Donnell CJ, Hirschhorn JN, Benjamin EJ. Contribution of clinical correlates and 13 C-reactive protein gene polymorphisms to interindividual variability in serum C-reactive protein level. Circulation. 113: 1415-23. PMID 16534007 DOI: 10.1161/Circulationaha.105.591271  0.303
2006 Fox CS, Larson MG, Vasan RS, Guo CY, Parise H, Levy D, Leip EP, O'donnell CJ, D'Agostino RB, Benjamin EJ. Cross-sectional association of kidney function with valvular and annular calcification: the Framingham heart study. Journal of the American Society of Nephrology : Jasn. 17: 521-7. PMID 16382018 DOI: 10.1681/Asn.2005060627  0.332
2005 Guo CY, Cui J, Cupples LA. Impact of non-ignorable missingness on genetic tests of linkage and/or association using case-parent trios. Bmc Genetics. 6: S90. PMID 16451706 DOI: 10.1186/1471-2156-6-S1-S90  0.315
2005 Yang Q, Guo CY, Cupples LA, Levy D, Wilson PW, Fox CS. Genome-wide search for genes affecting serum uric acid levels: the Framingham Heart Study. Metabolism: Clinical and Experimental. 54: 1435-41. PMID 16253630 DOI: 10.1016/J.Metabol.2005.05.007  0.344
2005 Fox CS, Yang Q, Cupples LA, Guo CY, Atwood LD, Murabito JM, Levy D, Mendelsohn ME, Housman DE, Shearman AM. Sex-specific association between estrogen receptor-alpha gene variation and measures of adiposity: the Framingham Heart Study. The Journal of Clinical Endocrinology and Metabolism. 90: 6257-62. PMID 16144952 DOI: 10.1210/Jc.2005-0670  0.374
2005 Kathiresan S, Larson MG, Vasan RS, Guo CY, Vita JA, Mitchell GF, Keyes MJ, Newton-Cheh C, Musone SL, Lochner AL, Drake JA, Levy D, O'Donnell CJ, Hirschhorn JN, Benjamin EJ. Common genetic variation at the endothelial nitric oxide synthase locus and relations to brachial artery vasodilator function in the community. Circulation. 112: 1419-27. PMID 16129794 DOI: 10.1161/Circulationaha.105.544619  0.386
2005 Guo CY, DeStefano AL, Lunetta KL, Dupuis J, Cupples LA. Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios. Human Heredity. 59: 125-35. PMID 15867473 DOI: 10.1159/000085571  0.328
2005 Gainer JV, Bellamine A, Dawson EP, Womble KE, Grant SW, Wang Y, Cupples LA, Guo CY, Demissie S, O'Donnell CJ, Brown NJ, Waterman MR, Capdevila JH. Functional variant of CYP4A11 20-hydroxyeicosatetraenoic acid synthase is associated with essential hypertension. Circulation. 111: 63-9. PMID 15611369 DOI: 10.1161/01.Cir.0000151309.82473.59  0.557
2005 Fox CS, Yang Q, Guo CY, Cupples LA, Wilson PW, Levy D, Meigs JB. Genome-wide linkage analysis to urinary microalbuminuria in a community-based sample: the Framingham Heart Study. Kidney International. 67: 70-4. PMID 15610229 DOI: 10.1111/J.1523-1755.2005.00056.X  0.398
2004 Fox CS, Yang Q, Cupples LA, Guo CY, Larson MG, Leip EP, Wilson PW, Levy D. Genomewide linkage analysis to serum creatinine, GFR, and creatinine clearance in a community-based population: the Framingham Heart Study. Journal of the American Society of Nephrology : Jasn. 15: 2457-61. PMID 15339995 DOI: 10.1097/01.Asn.0000135972.13396.6F  0.378
2003 Yang Q, Chazaro I, Cui J, Guo CY, Demissie S, Larson M, Atwood LD, Cupples LA, DeStefano AL. Genetic analyses of longitudinal phenotype data: a comparison of univariate methods and a multivariate approach. Bmc Genetics. 4: S29. PMID 14975097 DOI: 10.1186/1471-2156-4-S1-S29  0.58
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