Browsing by Author Ralston, Stuart H

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Issue DateTitleAuthor(s)Citation
2010Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of boneHooper, Michael; Albagha, Omar M E; Alonso, Nerea; Cundy, Tim; Dargie, Rosemary; del Pino Montes, Javier; di Stefano, Marco; Dunlop, Malcolm G; Fraser, William D; Gonzalez-Sarmiento, Rogelio; Isaia, Gianluca; Langston, Anne L; Nicholson, Geoff C; Ralston, Stuart H; Tenesa, Albert; Visconti, Micaela R; Walsh, John P; Concord Clinical School: MedicineGenome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone, Nature Genetics, vol.42, 6,pp 520-524
2005Ubiquitin-Associated Domain Mutations of SQSTM1 in Paget’s Disease of Bone: Evidence for a Founder Effect in Patients of British DescentHooper, Michael; Meier, Christian; Cundy, Tim; Daroszewska, Anna; Fraser, William D; Hocking, Lynne J; Lucas, Gavin JA; Nicholson, Geoff C; Ralston, Stuart H; Walsh, John P; Concord Clinical School: Medicine; MedicineUbiquitin-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 2005, vol.20,(2),2005,pp 227-231