Validity of 12-Month Falls Recall in Community-Dwelling Older Women Participating in a Clinical Trial

Por Sanders, Kerrie M., Stuart, Amanda L., Scott, David, Kotowicz, Mark A., Nicholson, Geoff C.
Publicado no Int J Endocrinol (2015)

Polyalanine Repeat Polymorphism in RUNX2 Is Associated with Site-Specific Fracture in Post-Menopausal Females

Por Morrison, Nigel A., Stephens, Alexandre S., Osato, Motomi, Pasco, Julie A., Fozzard, Nicolette, Stein, Gary S., Polly, Patsie, Griffiths, Lyn R., Nicholson, Geoff C.
Publicado em 2013

Does an increase in body mass index over 10 years affect knee structure in a population-based cohort study of adult women?

Por Brennan, Sharon L, Cicuttini, Flavia M, Pasco, Julie A, Henry, Margaret J, Wang, Yuanyuan, Kotowicz, Mark A, Nicholson, Geoff C, Wluka, Anita E
Publicado em 2010

Genomewide Search in Familial Paget Disease of Bone Shows Evidence of Genetic Heterogeneity with Candidate Loci on Chromosomes 2q36, 10p13, and 5q35

Por Hocking, Lynne J., Herbert, Craig A., Nicholls, Rosie K., Williams, Fiona, Bennett, Simon T., Cundy, Tim, Nicholson, Geoff C., Wuyts, Wim, Van Hul, Wim, Ralston, Stuart H.
Publicado em 2001

Oncostatin M promotes bone formation independently of resorption when signaling through leukemia inhibitory factor receptor in mice

Por Walker, Emma C., McGregor, Narelle E., Poulton, Ingrid J., Solano, Melissa, Pompolo, Sueli, Fernandes, Tania J., Constable, Matthew J., Nicholson, Geoff C., Zhang, Jian-Guo, Nicola, Nicos A., Gillespie, Matthew T., Martin, T. John, Sims, Natalie A.
Publicado em 2010

Glutamine Repeat Variants in Human RUNX2 Associated with Decreased Femoral Neck BMD, Broadband Ultrasound Attenuation and Target Gene Transactivation

Por Morrison, Nigel A., Stephens, Alexandre A., Osato, Motomi, Polly, Patsie, Tan, Timothy C., Yamashita, Namiko, Doecke, James D., Pasco, Julie, Fozzard, Nicolette, Jones, Graeme, Ralston, Stuart H., Sambrook, Philip N., Prince, Richard L., Nicholson, Geoff C.
Publicado em 2012

Genome wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget’s disease of bone

Por Albagha, Omar ME, 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, Ralston, Stuart H
Publicado em 2010