Hopper JL - Search Results

1

Clinical classification of BRCA1 and BRCA2 DNA sequence variants: the value of cytokeratin profiles and evolutionary analysis--a report from the kConFab Investigators.

Spurdle AB, Lakhani SR, Healey S, Parry S, Da Silva LM, Brinkworth R, Hopper JL, Brown MA, Babikyan D, Chenevix-Trench G, Tavtigian SV, Goldgar DE; kConFab Investigators. Spurdle AB, et al. Among authors: hopper jl. J Clin Oncol. 2008 Apr 1;26(10):1657-63. doi: 10.1200/JCO.2007.13.2779. J Clin Oncol. 2008. PMID: 18375895

2

Dominant negative ATM mutations in breast cancer families.

Chenevix-Trench G, Spurdle AB, Gatei M, Kelly H, Marsh A, Chen X, Donn K, Cummings M, Nyholt D, Jenkins MA, Scott C, Pupo GM, Dörk T, Bendix R, Kirk J, Tucker K, McCredie MR, Hopper JL, Sambrook J, Mann GJ, Khanna KK. Chenevix-Trench G, et al. Among authors: hopper jl. J Natl Cancer Inst. 2002 Feb 6;94(3):205-15. doi: 10.1093/jnci/94.3.205. J Natl Cancer Inst. 2002. PMID: 11830610

3

The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years.

Spurdle AB, Hopper JL, Chen X, Dite GS, Cui J, McCredie MR, Giles GG, Ellis-Steinborner S, Venter DJ, Newman B, Southey MC, Chenevix-Trench G. Spurdle AB, et al. Among authors: hopper jl. Cancer Epidemiol Biomarkers Prev. 2002 Apr;11(4):413-6. Cancer Epidemiol Biomarkers Prev. 2002. PMID: 11927503

4

The progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of breast cancer in Australian women.

Spurdle AB, Hopper JL, Chen X, McCredie MR, Giles GG, Venter DJ, Southey MC, Chenevix-Trench G. Spurdle AB, et al. Among authors: hopper jl. Cancer Epidemiol Biomarkers Prev. 2002 May;11(5):439-43. Cancer Epidemiol Biomarkers Prev. 2002. PMID: 12010857

5

The CYP3A4*1B polymorphism has no functional significance and is not associated with risk of breast or ovarian cancer.

Spurdle AB, Goodwin B, Hodgson E, Hopper JL, Chen X, Purdie DM, McCredie MR, Giles GG, Chenevix-Trench G, Liddle C. Spurdle AB, et al. Among authors: hopper jl. Pharmacogenetics. 2002 Jul;12(5):355-66. doi: 10.1097/00008571-200207000-00003. Pharmacogenetics. 2002. PMID: 12142725

6

Prohibitin 3' untranslated region polymorphism and breast cancer risk in Australian women.

Spurdle AB, Hopper JL, Chen X, McCredie MR, Giles GG, Newman B, Chenevix-Trench G. Spurdle AB, et al. Among authors: hopper jl. Lancet. 2002 Sep 21;360(9337):925-6. doi: 10.1016/S0140-6736(02)11043-9. Lancet. 2002. PMID: 12354477

7

BRCA2 Arg372Hispolymorphism and epithelial ovarian cancer risk.

Auranen A, Spurdle AB, Chen X, Lipscombe J, Purdie DM, Hopper JL, Green A, Healey CS, Redman K, Dunning AM, Pharoah PD, Easton DF, Ponder BA, Chenevix-Trench G, Novik KL. Auranen A, et al. Among authors: hopper jl. Int J Cancer. 2003 Jan 20;103(3):427-30. doi: 10.1002/ijc.10814. Int J Cancer. 2003. PMID: 12471628 Free article.

8

No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer.

Spurdle AB, Hopper JL, Chen X, McCredie MR, Giles GG, Newman B, Chenevix-Trench G, Khanna K. Spurdle AB, et al. Among authors: hopper jl. Breast Cancer Res. 2002;4(6):R15. doi: 10.1186/bcr534. Epub 2002 Aug 21. Breast Cancer Res. 2002. PMID: 12473176 Free PMC article.

9

Regressive logistic and proportional hazards disease models for within-family analyses of measured genotypes, with application to a CYP17 polymorphism and breast cancer.

Cui JS, Spurdle AB, Southey MC, Dite GS, Venter DJ, McCredie MR, Giles GG, Chenevix-Trench G, Hopper JL. Cui JS, et al. Among authors: hopper jl. Genet Epidemiol. 2003 Apr;24(3):161-72. doi: 10.1002/gepi.10222. Genet Epidemiol. 2003. PMID: 12652520

10

Uptake of offer to receive genetic information about BRCA1 and BRCA2 mutations in an Australian population-based study.

Keogh LA, Southey MC, Maskiell J, Young MA, Gaff CL, Kirk J, Tucker KM, Rosenthal D, McCredie MR, Giles GG, Hopper JL. Keogh LA, et al. Among authors: hopper jl. Cancer Epidemiol Biomarkers Prev. 2004 Dec;13(12):2258-63. Cancer Epidemiol Biomarkers Prev. 2004. PMID: 15598789

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