Scott RJ - Search Results

1

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.

Talseth-Palmer BA, Holliday EG, Evans TJ, McEvoy M, Attia J, Grice DM, Masson AL, Meldrum C, Spigelman A, Scott RJ. Talseth-Palmer BA, et al. Among authors: scott rj. BMC Med Genomics. 2013 Mar 26;6:10. doi: 10.1186/1755-8794-6-10. BMC Med Genomics. 2013. PMID: 23531357 Free PMC article.

2

Tumour site, sex, and survival in colorectal cancer.

Scott RJ, Spigelman AD. Scott RJ, et al. Lancet. 2000 Sep 2;356(9232):857; author reply 858. doi: 10.1016/S0140-6736(05)73439-5. Lancet. 2000. PMID: 11022958 No abstract available.

3

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds.

Scott RJ, McPhillips M, Meldrum CJ, Fitzgerald PE, Adams K, Spigelman AD, du Sart D, Tucker K, Kirk J. Scott RJ, et al. Am J Hum Genet. 2001 Jan;68(1):118-127. doi: 10.1086/316942. Epub 2000 Dec 7. Am J Hum Genet. 2001. PMID: 11112663 Free PMC article.

4

Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity.

Scott RJ, Meldrum C, Crooks R, Spigelman AD, Kirk J, Tucker K, Koorey D; Hunter Family Cancer Service. Scott RJ, et al. Gut. 2001 Apr;48(4):508-14. doi: 10.1136/gut.48.4.508. Gut. 2001. PMID: 11247895 Free PMC article.

5

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.

Scott RJ, Crooks R, Meldrum CJ, Thomas L, Smith CJ, Mowat D, McPhillips M, Spigelman AD. Scott RJ, et al. Clin Genet. 2002 Oct;62(4):282-7. doi: 10.1034/j.1399-0004.2002.620405.x. Clin Genet. 2002. PMID: 12372054

6

BRCA2 mutations in a population-based series of patients with ocular melanoma.

Scott RJ, Vajdic CM, Armstrong BK, Ainsworth CJ, Meldrum CJ, Aitken JF, Kricker A. Scott RJ, et al. Int J Cancer. 2002 Nov 10;102(2):188-91. doi: 10.1002/ijc.10693. Int J Cancer. 2002. PMID: 12385017

7

Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations.

Thompson E, Meldrum CJ, Crooks R, McPhillips M, Thomas L, Spigelman AD, Scott RJ. Thompson E, et al. Among authors: scott rj. Clin Genet. 2004 Mar;65(3):215-25. doi: 10.1111/j.1399-0004.2004.00214.x. Clin Genet. 2004. PMID: 14756672

8

Phenotype-genotype correlations in a series of wolfram syndrome families.

Smith CJ, Crock PA, King BR, Meldrum CJ, Scott RJ. Smith CJ, et al. Among authors: scott rj. Diabetes Care. 2004 Aug;27(8):2003-9. doi: 10.2337/diacare.27.8.2003. Diabetes Care. 2004. PMID: 15277431

9

Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations.

Kairupan CF, Meldrum CJ, Crooks R, Milward EA, Spigelman AD, Burgess B, Groombridge C, Kirk J, Tucker K, Ward R, Williams R, Scott RJ. Kairupan CF, et al. Among authors: scott rj. Int J Cancer. 2005 Aug 10;116(1):73-7. doi: 10.1002/ijc.20983. Int J Cancer. 2005. PMID: 15761860

10

Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53.

Talseth BA, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott RJ. Talseth BA, et al. Among authors: scott rj. Int J Cancer. 2006 May 15;118(10):2479-84. doi: 10.1002/ijc.21661. Int J Cancer. 2006. PMID: 16353134

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