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Issue DateTitleAuthor(s)
2011-02-01Contribution of a common variant in the promoter of the 1-α-hydroxylase gene (CYP27B1) to fracture risk in the elderlyClifton-Bligh, RJ; Nguyen, TV; Au, A; Bullock, M; Cameron, I; Cumming, R; Chen, JS; March, LM; Seibel, MJ; Sambrook, PN
2016-03Pheo-Type: A Diagnostic Gene-expression Assay for the Classification of Pheochromocytoma and Paraganglioma.Flynn, A; Dwight, T; Harris, J; Benn, D; Zhou, L; Hogg, A; Catchpoole, D; James, P; Duncan, EL; Trainer, A; Gill, AJ; Clifton-Bligh, R; Hicks, RJ; Tothill, RW
2021Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults With Rhabdomyosarcoma.Kim, J; Light, N; Subasri, V; Young, EL; Wegman-Ostrosky, T; Barkauskas, DA; Hall, D; Lupo, PJ; Patidar, R; Maese, LD; Jones, K; Wang, M; Tavtigian, SV; Wu, D; Shlien, A; Telfer, F; Goldenberg, A; Skapek, SX; Wei, JS; Wen, X; Catchpoole, D; Hawkins, DS; Schiffman, JD; Khan, J; Malkin, D; Stewart, DR
2008-12-01Pharmacogenetics of osteoporosis and the prospect of individualized prognosis and individualized therapyNguyen, TV; Center, JR; Eisman, JA
2009-11-01Enhancement of absolute fracture risk prognosis with genetic marker: The collagen i alpha 1 geneTran, BNH; Nguyen, ND; Center, JR; Eisman, JA; Nguyen, TV
2019-12-01GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fracturesStyrkarsdottir, U; Stefansson, OA; Gunnarsdottir, K; Thorleifsson, G; Lund, SH; Stefansdottir, L; Juliusson, K; Agustsdottir, AB; Zink, F; Halldorsson, GH; Ivarsdottir, EV; Benonisdottir, S; Jonsson, H; Gylfason, A; Norland, K; Trajanoska, K; Boer, CG; Southam, L; Leung, JCS; Tang, NLS; Kwok, TCY; Lee, JSW; Ho, SC; Byrjalsen, I; Center, JR; Lee, SH; Koh, JM; Lohmander, LS; Ho-Pham, LT; Nguyen, TV; Eisman, JA; Woo, J; Leung, PC; Loughlin, J; Zeggini, E; Christiansen, C; Rivadeneira, F; van Meurs, J; Uitterlinden, AG; Mogensen, B; Ingvarsson, T; Sigurdsson, G; Benediktsson, R; Sulem, P; Jonsdottir, I; Masson, G; Holm, H; Norddahl, GL; Thorsteinsdottir, U; Gudbjartsson, DF; Stefansson, K
2016-07Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease.Zhou, F; Cao, H; Zuo, X; Zhang, T; Zhang, X; Liu, X; Xu, R; Chen, G; Zhang, Y; Zheng, X; Jin, X; Gao, J; Mei, J; Sheng, Y; Li, Q; Liang, B; Shen, J; Shen, C; Jiang, H; Zhu, C; Fan, X; Xu, F; Yue, M; Yin, X; Ye, C; Zhang, C; Liu, X; Yu, L; Wu, J; Chen, M; Zhuang, X; Tang, L; Shao, H; Wu, L; Li, J; Xu, Y; Zhang, Y; Zhao, S; Wang, Y; Li, G; Xu, H; Zeng, L; Wang, J; Bai, M; Chen, Y; Chen, W; Kang, T; Wu, Y; Xu, X; Zhu, Z; Cui, Y; Wang, Z; Yang, C; Wang, P; Xiang, L; Chen, X; Zhang, A; Gao, X; Zhang, F; Xu, J; Zheng, M; Zheng, J; Zhang, J; Yu, X; Li, Y; Yang, S; Yang, H; Wang, J; Liu, J; Hammarström, L; Sun, L; Wang, J; Zhang, X
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