Browsing by Author Thorne, Heather

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Issue DateTitleAuthor(s)Citation
2006Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resourceBalleine, Rosemary; Butow, Phyllis; Clarke, Christine; Kirk, Judy; Leary, Jennifer; Mann, Graham; Pupo, Gulietta; Chenevix-Trench, Georgia; Edkins, Edward; Evans, Gerda M.; Fereday, Sian; Gattas, Michael; Giles, Graham; Goldblatt, Jack; Haan, Eric; Hopper, John; Lindeman, Geoffrey J; Niedermayr, Eveline; Phillips, Kelly-Anne; Picken, Sandra; Saunders, Christobel; Scott, Clare L; Spurdle, Amanda B.; Suthers, Graeme; The Kathleen Cuningham Consortium for Research in Familial Breast Cancer, kConFab; Thorne, Heather; Tucker, Katherine M.; Western Clinical School: Medicine (Westmead); Psychology; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead)Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource, Breast Cancer Research, vol.8,(1),2006,pp N/A-N/A
2006Histopathological features of breast cancer in carriers of ATM gene variants.Balleine, Rosemary; Bilous, Michael; Byth Wilson, Karen; Kirk, Judy; Provan, Pamela; Farshid, Gelareh; KConFab, Consortium; Murali, R; Thorne, Heather; Waring, Paul; Western Clinical School: Medicine (Westmead); Western Clinical School: Medicine (Westmead); School of Public Health: NH&MRC Clinical Trials Centre; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium InstituteHistopathological features of breast cancer in carriers of ATM gene variants., Histopathology, vol.49,(5),2006,pp 523-532
2013Improving mutation notification when new genetic information is identified in research: a trial of two strategies in familial breast cancerKirk, Judy; Doolan, Emma L; Niedermayr, Eveline; Thorne, Heather; Tucker, Kathy; Wakefield, Claire E.; Western Clinical School: Westmead Millennium InstituteImproving mutation notification when new genetic information is identified in research: a trial of two strategies in familial breast cancer, Genetics in Medicine, vol.15, 3, 2013,pp 187-194
2014Multifactorial likelihood assessment of BRCA1 and BRCA2 missense variants confirms that RCA1:c.122A>G(p.His41Arg) is a pathogenic mutationLeary, Jennifer; Dopita, Belinda; Lakhani, Sunil R.; Parsons, Michael T; Thorne, Heather; Tucker, K; Warwick, Linda; Whiley, Phillip J; Western Clinical School: Medicine (Westmead)Multifactorial likelihood assessment of BRCA1 and BRCA2 missense variants confirms that RCA1:c.122A>G(p.His41Arg) is a pathogenic mutation, PloS One, vol.9, 1, 2014,pp e86836-N/A