Ralston SH - Search Results

1

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

Albagha OM, Visconti MR, Alonso N, Langston AL, Cundy T, Dargie R, Dunlop MG, Fraser WD, Hooper MJ, Isaia G, Nicholson GC, del Pino Montes J, Gonzalez-Sarmiento R, di Stefano M, Tenesa A, Walsh JP, Ralston SH. Albagha OM, et al. Among authors: ralston sh. Nat Genet. 2010 Jun;42(6):520-4. doi: 10.1038/ng.562. Epub 2010 May 2. Nat Genet. 2010. PMID: 20436471 Free PMC article.

2

Hypercalcaemia in rheumatoid arthritis revisited.

Ralston SH, Fraser WD, Jankowski J, Richards IM, Cowan RA, Capell HA, Sturrock RD. Ralston SH, et al. Ann Rheum Dis. 1990 Jan;49(1):22-4. doi: 10.1136/ard.49.1.22. Ann Rheum Dis. 1990. PMID: 2310223 Free PMC article.

3

'Apathetic' thyrotoxicosis presenting with hypercalcaemia and spurious normalization of serum thyroid hormone levels.

Ralston SH, Fraser WD, Soukop M, McKillop JH. Ralston SH, et al. Postgrad Med J. 1987 Apr;63(738):269-71. doi: 10.1136/pgmj.63.738.269. Postgrad Med J. 1987. PMID: 2446302 Free PMC article.

4

Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis.

Hughes AE, Ralston SH, Marken J, Bell C, MacPherson H, Wallace RG, van Hul W, Whyte MP, Nakatsuka K, Hovy L, Anderson DM. Hughes AE, et al. Among authors: ralston sh. Nat Genet. 2000 Jan;24(1):45-8. doi: 10.1038/71667. Nat Genet. 2000. PMID: 10615125

5

Familial Paget's disease of bone: patterns of inheritance and frequency of linkage to chromosome 18q.

Hocking L, Slee F, Haslam SI, Cundy T, Nicholson G, van Hul W, Ralston SH. Hocking L, et al. Among authors: ralston sh. Bone. 2000 Jun;26(6):577-80. doi: 10.1016/s8756-3282(00)00278-7. Bone. 2000. PMID: 10831928

6

Estrogen receptor alpha gene polymorphisms and bone mineral density: haplotype analysis in women from the United Kingdom.

Albagha OM, McGuigan FE, Reid DM, Ralston SH. Albagha OM, et al. Among authors: ralston sh. J Bone Miner Res. 2001 Jan;16(1):128-34. doi: 10.1359/jbmr.2001.16.1.128. J Bone Miner Res. 2001. PMID: 11149476 Free article.

7

Evaluation of the role of RANK and OPG genes in Paget's disease of bone.

Wuyts W, Van Wesenbeeck L, Morales-Piga A, Ralston S, Hocking L, Vanhoenacker F, Westhovens R, Verbruggen L, Anderson D, Hughes A, Van Hul W. Wuyts W, et al. Bone. 2001 Jan;28(1):104-7. doi: 10.1016/s8756-3282(00)00411-7. Bone. 2001. PMID: 11165949

8

Mutation screening of the TNFRSF11A gene encoding receptor activator of NF kappa B (RANK) in familial and sporadic Paget's disease of bone and osteosarcoma.

Sparks AB, Peterson SN, Bell C, Loftus BJ, Hocking L, Cahill DP, Frassica FJ, Streeten EA, Levine MA, Fraser CM, Adams MD, Broder S, Venter JC, Kinzler KW, Vogelstein B, Ralston SH. Sparks AB, et al. Among authors: ralston sh. Calcif Tissue Int. 2001 Mar;68(3):151-5. doi: 10.1007/s002230001211. Calcif Tissue Int. 2001. PMID: 11351498

9

Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.

Hocking LJ, Herbert CA, Nicholls RK, Williams F, Bennett ST, Cundy T, Nicholson GC, Wuyts W, Van Hul W, Ralston SH. Hocking LJ, et al. Among authors: ralston sh. Am J Hum Genet. 2001 Nov;69(5):1055-61. doi: 10.1086/323798. Epub 2001 Sep 5. Am J Hum Genet. 2001. PMID: 11555792 Free PMC article.

10

Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women.

Albagha OM, Tasker PN, McGuigan FE, Reid DM, Ralston SH. Albagha OM, et al. Among authors: ralston sh. Hum Mol Genet. 2002 Sep 15;11(19):2289-95. doi: 10.1093/hmg/11.19.2289. Hum Mol Genet. 2002. PMID: 12217957 Free article.

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