Ralston SH - Search Results

1

Identification of sex-specific associations between polymorphisms of the osteoprotegerin gene, TNFRSF11B, and Paget's disease of bone.

Beyens G, Daroszewska A, de Freitas F, Fransen E, Vanhoenacker F, Verbruggen L, Zmierczak HG, Westhovens R, Van Offel J, Ralston SH, Devogelaer JP, Van Hul W. Beyens G, et al. Among authors: ralston sh. J Bone Miner Res. 2007 Jul;22(7):1062-71. doi: 10.1359/jbmr.070333. J Bone Miner Res. 2007. PMID: 17388729 Free article.

2

Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity.

Haslam SI, Van Hul W, Morales-Piga A, Balemans W, San-Millan JL, Nakatsuka K, Willems P, Haites NE, Ralston SH. Haslam SI, et al. Among authors: ralston sh. J Bone Miner Res. 1998 Jun;13(6):911-7. doi: 10.1359/jbmr.1998.13.6.911. J Bone Miner Res. 1998. PMID: 9626621 Free article.

3

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

4

Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13.

Janssens K, Gershoni-Baruch R, Van Hul E, Brik R, Guañabens N, Migone N, Verbruggen LA, Ralston SH, Bonduelle M, Van Maldergem L, Vanhoenacker F, Van Hul W. Janssens K, et al. Among authors: ralston sh. J Med Genet. 2000 Apr;37(4):245-9. doi: 10.1136/jmg.37.4.245. J Med Genet. 2000. PMID: 10745041 Free PMC article.

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

Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease.

Janssens K, Gershoni-Baruch R, Guañabens N, Migone N, Ralston S, Bonduelle M, Lissens W, Van Maldergem L, Vanhoenacker F, Verbruggen L, Van Hul W. Janssens K, et al. Nat Genet. 2000 Nov;26(3):273-5. doi: 10.1038/81563. Nat Genet. 2000. PMID: 11062463

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

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.

Hocking LJ, Lucas GJ, Daroszewska A, Mangion J, Olavesen M, Cundy T, Nicholson GC, Ward L, Bennett ST, Wuyts W, Van Hul W, Ralston SH. Hocking LJ, et al. Among authors: ralston sh. Hum Mol Genet. 2002 Oct 15;11(22):2735-9. doi: 10.1093/hmg/11.22.2735. Hum Mol Genet. 2002. PMID: 12374763

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