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Reid, Ian R., Nicholson, Geoffrey C., Weinstein, Robert S., Hosking, David J., Cundy, Tim, Kotowicz, Mark A., Murphy, William A., Yeap, Swan, Dufresne, Suzanne, Lombardi, Antonio, Musliner, Thomas A., Thompson, Desmond E. and Yates, A. John (1996) Biochemical and radiologic improvement in Paget's disease of bone treated with alendronate: A randomized, placebo-controlled trial. American Journal of Medicine, 101 4: 341-348. doi:10.1016/S0002-9343(96)00227-6 39   90 Cited 119 times in Scopus119 0
Naot, Dorit, Bava, Usha, Matthews, Brya, Callon, Karen E, Gamble, Gamble D, Black, Michael, Song, Sarah, Pitto, Rocco P, Cundy, Tim, Cornish, Jill and Reid, Ian R (2006) Differential gene expression in cultured osteoblasts and bone marrow stromal cells from patients with Pagetís disease of bone. Journal of Bone and Mineral Research, 22 2: 298-309. doi:10.1359/JBMR.061108 73   45 Cited 53 times in Scopus53 0
Hocking, Lynne J., Lucas, Gavin J. A., Daroszewska, Anna, Mangion, Jon, Olavesen, Mark, Cundy, Tim, Nicholson, Geoff C., Ward, Lynley, Bennett, Simon T., Wuyts, Wim, Van Hul, Wim and Ralston, Stuart H. (2002) Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease. Human Molecular Genetics, 11 22: 2735-2739. doi:10.1093/hmg/11.22.2735 37   165 Cited 186 times in Scopus186 0
Lucas, Gavin J. A., Mehta, Sarju G., Hocking, Lynne J., Stewart, Tracey L., Cundy, Tim, Nicholson, Geoffrey C., Walsh, John P., Fraser, William D., Watts, Giles D. J., Ralston, Stuart H. and Kimonis, Virginia E. (2006) Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone. Bone, 38 2: 280-285. doi:10.1016/j.bone.2005.07.014 41   20 Cited 25 times in Scopus25 3
Albagha, Ommar M. E., Wani, Sachin E., Visconti, Micaela R., Alonso, Nerea, Goodman, Kirsteen, Brandi, Maria Luisa, Cundy, Tim, Chung, Pui Yan Jenny, Dargie, Rosemary, Devogelaer, Jean-Pierre, Falchetti, Alberto, Fraser, William D., Gennari, Luigi, Gianfrancesco, Fernando, Hooper, Michael J., Van Hul, Wim, Isaia, Gianluca, Nicholson, Geoff C., Nuti, Ranuccio, Papapoulos, Socrates, Montes, Javier del Pino, Ratajczak, Thomas, Rea, Sarah L., Rendina, Domenico, Gonzalez-Sarmiento, Rogelio, Di Stefano, Marco, Ward, Lynley C., Walsh, John P., Ralston, Stuart H. and Genetic Determinants of Paget's Disease (GDPD) Consortium (2011) Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. Nature Genetics, 43 7: 685-689. doi:10.1038/ng.845 72   35 Cited 41 times in Scopus41 2
Albagha, Omar, Fraser, William, Gennari, Luigi, Hooper, Michael, Van Hul, Wim, Isaia, Gianluca, Nicholson, Geoff, Papapoulos, Socrates, Montes, Javier del Pino, Gonzalez-Sarmiento, Rogelio, di Stefano, Marco, Wani, Sachin, Walsh, John, Ralston, Stuart for the GDPD Consortium, Visconti, Micaela, Alonso, Nerea, Goodman, Kristeen, Brandi, Maria Luisa, Cundy, Tim, Dargie, Rosemary and Falchetti, Alberto (2011). Genome wide association study identifies seven loci that account for 86% of the population attributable risk of Paget's disease of bone. In: 1stIOF-ESCEO Pre-Clinical Symposium Oral Communication Abstracts. 1st IOF-ESCEO Pre-Clinical Symposium, Valencia, Spain, (12-12). 23-26 March 2011. doi:10.1007/s00198-011-1564-7 138   0 0
Albagha, Omar M. E., Visconti, Micaela R., Alonso, Nerea, Langston, Anne L., Cundy, Tim, Dargie, Rosemary, Dunlop, Malcolm G., Fraser, William D., Hooper, Michael J., Isaia, Gianluca, Nicholson, Geoff C., del Pino Montes, Javier, Gonzalez-Sarmiento, Rogelio, di Stefano, Marco, Tenesa, Albert, Walsh, John P. and Ralston, Stuart H. (2010) Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. Nature Genetics, 42 6: 520-525. doi:10.1038/ng.562 62   79 Cited 88 times in Scopus88 10
Hocking, Lynne J., Herbert, Craig A., Nicholls, Rosie K., Williams, Fiona, Bennett, Simon T., Cundy, Tim, Nicholson, Geoff C., Wuyts, Wim, Van Hul, Wim Van and Ralston, Stuart H. (2001) Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35. American Journal of Human Genetics, 69 5: 1055-1061. doi:10.1086/323798 39   70 Cited 84 times in Scopus84 0
Lucas, Gavin J. A., Riches, Phillip L., Hocking, Lynne J., Cundy, Tim, Nicholson, Geoffrey C., Walsh, John P. and Ralston, Stuart H. (2008) Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent. Journal of Bone And Mineral Research, 23 1: 58-63. doi:10.1359/JBMR.071004 39   22 Cited 25 times in Scopus25 0
Hocking, Lynne J., Lucas, Gavin J. A., Daroszewska, Anna, Cundy, Tim, Nicholson, Geoff C., Donath, Judit, Walsh, John P., Finlayson, Catriona, Cavey, James R., Ciani, Barbara, Sheppard, Paul W., Layfield, Robert and Ralston, Stuart H. (2004) Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: Genotype phenotype correlation, functional analysis, and structural consequences. Journal of Bone and Mineral Research, 19 7: 1122-1127. doi:10.1359/JBMR.0403015 26   93 Cited 109 times in Scopus109 0
Lucas, Gavin J. A., Hocking, Lynne J., Daroszewska, Anna, Cundy, Tim, Nicholson, Geoff C., Walsh, John P., Fraser, William D., Meier, Christian, Hooper, Michael J. and Ralston, Stuart H. (2005) Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: Evidence for a founder effect in patients of British descent. Journal of Bone And Mineral Research, 20 2: 227-231. doi:10.1359/JBMR.041106 36   30 Cited 35 times in Scopus35 0