Chao Xing, Ph.D.


Lin CY, Xing G, Ku HC, Elston RC, Xing C (2014) Enhancing the power to detect low-frequency variants in genome-wide screens. Genetics. 196:1293-1302

Garg A, Xing C (2014) De novo Heterozygous FBN1 Mutations in the Extreme C-terminal Region Cause Progeroid Fibrollinopathy. Am J Med Genet A. 164:1341-1345

Xing G, Ku HC, Xing C (2013) A comparison of the likelihood ratio test and the variance-stabilising transformation-based tests for detecting association of rare variants. Annals of Human Genetics. 77:333-335

Lin CY, Xing G, Xing C. (2012) Measuring linkage disequilibrium by the partial correlation coefficient. Heredity. 109:401-402

Xing G, Lin CY, Wooding SP, Xing C. (2012) Blindly Using Wald's Test Can Miss Rare Disease-Causal Variants in Case-Control Association Studies. Annals of Human Genetics. 76:168-77.

Xing G, Lin CY, Xing C. (2011) A comparison of approaches to control for confounding factors by regression models. Human Heredity.72:194-205

Xing C, Morris N, Xing G (2010) Distribution of model-based multipoint heterogeneity lod scores. Genetic Epidemiology. 34:912-916

Xing G, Xing C. (2010) Adjusting for covariates in logistic regression models. Genetic Epidemiology. 34:769-771

Agarwal AK, Xing C, DeMartino GN, Mizrachi D, Hernandez MD, Sousa AB, de Villarreal LM, dos Santos HG, Garg A (2010) PSMB8 encoding the ß5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia and panniculitis-induced lipodystrophy syndrome. American Journal of Human Genetics. 87:866-872

Xing C, Cohen JC, Boerwinkle E. (2010) A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels. American Journal of Human Genetics. 86:440-446