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A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27
Shen, H.; Zhang, YY; Long, JR; Xu, FH; Liu, YZ; Xiao, P.; Zhao, LJ; Xiong, DH; Liu, YJ; Dvornyk, V.; Rocha-Sanchez, S.; Liu, PY; Li, JL; Conway, T.; Davies, KM; Recker, RR; Deng, HW. A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27. Journal of medical genetics. 2004, OCT. 41(10):743-751.
A genomewide linkage scan for quantitative-trait loci for obesity phenotypes
Deng, HW; Deng, HY; Liu, YJ; Liu, YZ; Xu, FH; Shen, H.; Conway, T.; Li, JL; Huang, QY; Davies, KM; Recker, RR. A genomewide linkage scan for quantitative-trait loci for obesity phenotypes. American Journal of Human Genetics. 2002, MAY. 70(5):1138-1151.
CA repeat polymorphism of the TNFR2 gene is not associated with bone mineral density in two independent Caucasian populations
Huang, Q. Y.; Shen, H.; Deng, H. Y.; Conway, T.; Elze, L.; Davies, K. M.; Recker, R. R.; Deng, H. W. CA repeat polymorphism of the TNFR2 gene is not associated with bone mineral density in two independent Caucasian populations. Journal of bone and mineral metabolism. 2006, MAR. 24(2):132-137.
A follow-up linkage study for bone size variation in an extended sample
Xu, Fu-Hua; Liu, Yong-Jun; Deng, Hongyi; Huang, Qing-Yang; Zhao, Lan-Juan; Shen, Hui; Liu, Yao-Zhong; Dvornyk, Volodymyr; Conway, Theresa; Li, Jin-Long; Davies, K. M.; Recker, Robert R.; Deng, Hong-Wen. A follow-up linkage study for bone size variation in an extended sample. Bone. 2004, SEP. 35(3):777-784.
A whole-genome linkage scan suggests several genomic regions potentially containing quantitative trait loci for osteoporosis
Deng, HW; Xu, FH; Huang, QY; Shen, H.; Deng, HY; Conway, T.; Liu, YJ; Liu, YZ; Li, JL; Zhang, HT; Davies, KM; Recker, RR. A whole-genome linkage scan suggests several genomic regions potentially containing quantitative trait loci for osteoporosis. Journal of Clinical Endocrinology & Metabolism. 2002, NOV. 87(11):5151-5159.
Several genomic regions potentially containing QTLs for bone size variation were identified in a whole-genome linkage scan
Deng, HW; Shen, H.; Xu, FH; Deng, HY; Conway, T.; Liu, YJ; Liu, YZ; Li, JL; Huang, QY; Davies, KM; Recker, RR. Several genomic regions potentially containing QTLs for bone size variation were identified in a whole-genome linkage scan. American Journal of Medical Genetics Part a. 2003, JUN 1. 119A(2):121-131.
A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature
Deng, HW; Xu, FH; Liu, YZ; Shen, H.; Deng, HY; Huang, QY; Liu, YJ; Conway, T.; Li, JL; Davies, KM; Recker, RR. A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature. American Journal of Medical Genetics. 2002, NOV 15. 113(1):29-39.
A second-stage genome scan for QTLs influencing BMD variation
Huang, QY; Xu, FH; Shen, H.; Zhao, LJ; Deng, HY; Liu, YJ; Dvomyk, V.; Conway, T.; Davies, KM; Li, JL; Liu, YZ; Recker, RR; Deng, HW. A second-stage genome scan for QTLs influencing BMD variation. Calcified tissue international. 2004, AUG. 75(2):138-143.
Genome scan for QTLs underlying bone size variation at 10 refined skeletal sites: genetic heterogeneity and the significance of phenotype refinement
Huang, QY; Xu, FH; Shen, H.; Deng, HY; Conway, T.; Liu, YJ; Liu, YZ; Li, JL; Li, MX; Davies, KM; Recker, RR; Deng, HW. Genome scan for QTLs underlying bone size variation at 10 refined skeletal sites: genetic heterogeneity and the significance of phenotype refinement. Physiological Genomics. 2004, MAY 19. 17(3):326-331.
Confirmation linkage study in support of the X chromosome harbouring a QTL underlying human height variation
Liu, YZ; Xu, FH; Shen, H.; Deng, H.; Liu, YJ; Zhao, LJ; Dvornyk, V.; Conway, T.; Li, JL; Huang, QY; Davies, KM; Recker, RR; Deng, HW. Confirmation linkage study in support of the X chromosome harbouring a QTL underlying human height variation. Journal of medical genetics. 2003, NOV 1. 40(11):825-831.