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PreviewIssue DateTitleAuthor(s)
2001A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriersWang, W.; Spurdle, A.; Kolachana, P.; Bove, B.; Modan, B.; Ebbers, S.; Suthers, G.; Tucker, M.; Kaufman, D.; Doody, M.; Tarone, R.; Daly, M.; Levavi, H.; Pierce, H.; Chetrit, A.; Yechezkel, G.; Chenevix-Trench, G.; Offit, K.; Godwin, A.; Struewing, J.
2001Long-term outcomes of genetic counseling in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Barratt, A.; Schneiden, V.; Gattas, M.; Kirk, J.; Gaff, C.; Suthers, G.; Tucker, K.
2010Risks of Lynch Syndrome cancers for MSH6 mutation carriersSuthers, G.
2007Cancer risks for Australian women with a BRCA1 or a BRCA2 mutationSuthers, G.
2012Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): A new autosomal dominant syndromeWorthley, D.; Phillips, K.; Wayte, N.; Schrader, K.; Healey, S.; Kaurah, P.; Shulkes, A.; Grimpen, F.; Clouston, A.; Moore, D.; Cullen, D.; Ormonde, D.; Mounkley, D.; Wen, X.; Lindor, N.; Carniero, F.; Huntsman, D.; Chenevix-Trench, G.; Suthers, G.
2010Lynch syndrome-associated breast cancers: Clinicopathologic characteristics of a case series from the colon cancer family registryWalsh, M.; Buchanan, D.; Cummings, M.; Pearson, S.; Arnold, S.; Clendenning, M.; Walters, R.; McKeone, D.; Spurdle, A.; Hopper, J.; Jenkins, M.; Phillips, K.; Suthers, G.; George, J.; Goldblatt, J.; Muir, A.; Tucker, K.; Pelzer, E.; Gattas, M.; Woodall, S.; et al.
2010Risk factors for colorectal cancer in patients with multiple serrated polyps: A cross-sectional case series from genetics clinicsSuthers, G.; Aziz, S.A.
2005MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancerHitchins, M.; Williams, R.; Cheong, K.; Halani, N.; Lin, V.; Packham, D.; Ku, S.; Buckle, A.; Hawkins, N.; Burn, J.; Gallinger, S.; Goldblatt, J.; Kirk, J.; Tomlinson, I.; Scott, R.; Spigelman, A.; Suter, C.; Martin, D.; Suthers, G.; Ward, R.

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