Browse By Person: Spurdle, Amanda
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Number of items: 15.
Lose, Felicity, Srinivasan, Srilakshmi, O'Mara, Tracy, Marquart, Louise, Chambers, Suzanne, Gardiner, Robert, et al. (2012) Genetic association of the KLK4 locus with risk of prostate cancer. PLoS ONE, 7(9), e44520.
Lose, Felicity, Lawrence, Mitchell Graham, Srinivasan, Srilakshmi, O'Mara, Tracy, Marquart, Louise, Chambers, Suzanne, et al. (2012) Kallikrein 14 is down-regulated by androgen receptor signalling and harbours genetic variation that is associated with prostate tumour aggressiveness. Biological Chemistry, 393(5), pp. 403-412.
Amin Al Olama, A., Kote-Jarai, Z., Schumacher, F. R., Wiklund, F., Berndt, S. I., Benlloch, S., et al. (2012) A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease. Human Molecular Genetics, 22(2), pp. 408-415.
Chen, Alice Che-Ha, Keleher, Annie, Kedda, Mary-Anne, Spurdle, Amanda B., McMillan, Nigel, & Antonsson, Annika (2009) Human papillomavirus DNA detected in peripheral blood samples from healthy Australian male blood donors. Journal of Medical Virology, 81(10), pp. 1792-1796.
Kote-Jarai, Zsofia, Easton, Douglas F., Stanford, Janet L., Ostrander, Elaine A., Schleutker, Johanna, Ingles, Sue A., et al. (2008) Multiple novel prostate cancer predisposition loci confirmed by an international study : the PRACTICAL Consortium. Cancer Epidemiology Biomarkers and Prevention, 17(8), pp. 2052-2061.
Lose, Felicity, Duffy, David L., Kay, Graham F., Cuningham, Kathleen, Kedda, Mary A., & Spurdle, Amanda B. (2008) Skewed X chromosome inactivation and breast and ovarian cancer status : evidence for X-linked modifiers of BRCA1. Journal of the National Cancer Institute, 100(21), pp. 1519-1529.
Lai, John, Kedda, Mary-Anne, Hinze, Kimberly E., Smith, Robert L. G., Yaxley, John, Spurdle, Amanda B., et al. (2007) PSA/KLK3 AREI promoter polymorphism alters androgen receptor binding and is associated with prostate cancer susceptibility. Carcinogenesis, 28(5), pp. 1032-1039.
Pagan, Julia K., Arnold, Jeremy, Hanchard, Kim J., Kumar, Raman, Bruno, Tiziana, Jones, Mathew J. K., et al. (2007) A novel corepressor, BCoR-L1, represses transcription through an interaction with CtBP. Journal of Biological Chemistry, 282(20), pp. 15248-15257.
Marsh, Anna, Healey, Sue C., Lewis, Aaron, Spurdle, Amanda B., Kedda, Mary-Anne, Khanna, Kum Kum, et al. (2006) Mutation analysis of five candidate genes in familial breast cancer. Breast Cancer Research and Treatment, 105(3), pp. 377-389.
Chen, Xiaoqing, Chenevix-Trench, Georgia, Giles, Graham, Hopper, John, Kelemen, Livia, Newman, Beth, et al. (2005) Double-Strand Break Repair Gene Polymorphisms and Risk of Breast or Ovarian Cancer. Cancer Epidemiloogy Biomarkers and Prevention, 14(2), pp. 319-323.
Jekimovs, C.R., Chen, X., Arnold, J., Gatei, M., Richard, D.J., Spurdle, A.B., et al. (2005) Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families : functional analysis in heterozygous individuals. British Journal of Cancer, 92(4), pp. 784-790.
Antoniou, Antonis, Apicella, Carmel, Chen, Xiaoqing, Chevenix-Trench, Georgia, Cook, Margaret, Dite, Gillian, et al. (2004) The Androgen Receptor CAG Repeat Polymorphism and Modification of Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers. Breast Cancer Research, 7(2), pp. 176-183.
Spurdle, Amanda B., Hopper, John L., Chen, Xiaoqing, McCredie, Margaret R.E., Giles, Graham G., Newman, Beth M., et al. (2002) Prohibitin 3' untranslated region polymorphism and breast cancer risk in Australian women. The Lancet, 360(9337), pp. 925-926.
Chen, Xiaoging, Chenevix-Trench, Georgia, Cui, Jisheng, Dite, Gillian, Ellis-Steinborner, Sarah, Giles, Graham, et al. (2002) The BRCA2 372HH Genotype is Associated with Risk of Breast Cancer in Australian Women Under Age 60 Years. Cancer Epidemiology , Biomarkers & Prevention, 11, pp. 413-416.
Chen, Xiaoging, Chenevix-Trench, Georgia, Giles, Graham, Hopper, John, Kahanna, KumKum, McGredie, Margaret, et al. (2002) No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer. Breast Cancer Research, 4(6), pp. 1-6.