Browsing by Author Leary, Jennifer

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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
2017BRCA2 hypomorphic missense variants confer moderate risks of breast cancerLeary, Jennifer; Calleja, Fabienne; Ehlen, Asa; et al, Various; Guidugli, Lucia; Hallberg, Emily; Martin, Charlotte; Meeks, Huong; Mesman, R; Shimelis, Hermela; Von Nicolai, C; Western Clinical School: Medicine (Westmead)BRCA2 hypomorphic missense variants confer moderate risks of breast cancer, Cancer Research, vol.77, 11, 2017,pp 2789-2799
2006Evaluation of models to predict BRCA germline mutations.Kirk, Judy; Leary, Jennifer; Kang, H. H.; Ringland, Clare; Ward, Robyn N.; Williams, Rachel; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead)Evaluation of models to predict BRCA germline mutations., British Journal of Cancer, vol.95,(7),2006,pp 914-920
2004Frequency Of The Atm Ivs10-6T-->G Variant In Australian Multiple-Case Breast Cancer Families.Kirk, Judy; Leary, Jennifer; Cheetham, Glenice; Field, M.; Gaff, Clara L; Hiew, Melody; Lindeman, Geoffrey J; McKinlay Garnder, R J; Suthers, Graeme; Trainor, Kevin; Visvader, Jane E; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead)Frequency Of The Atm Ivs10-6T-->G Variant In Australian Multiple-Case Breast Cancer Families., Breast Cancer Research, vol.6,(4),2004,pp R401-7-N/A
2004Germ-Line Mutations In Brca1 Or Brca2 In The Normal Breast Are Associated With Altered Expression Of Estrogen-Responsive Proteins And The Predominance Of Progesterone Receptor A.Avery, Kelly; Clarke, Christine; Kirk, Judy; Leary, Jennifer; Mote, Patricia; Chenevix-Trench, Georgia; kConFab Investigators, PMCI; Sandelin, K; Nepean Clinical School: Office; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium InstituteGerm-Line Mutations In Brca1 Or Brca2 In The Normal Breast Are Associated With Altered Expression Of Estrogen-Responsive Proteins And The Predominance Of Progesterone Receptor A., Genes Chromosomes & Cancer, vol.39,(3),2004,pp 236-248
2005Large genomic rearrangements of both BRCA2 and BRCA1 are a feature of the inherited breast/ovarian cancer phenotype in selected familiesDavis, Tracey; Kirk, Judy; Leary, Jennifer; Silva, A; Woodward, Amanda; KConFab, Consortium; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead); Western Clinical School: Medicine (Westmead); Medicine Faculty OfficeLarge genomic rearrangements of both BRCA2 and BRCA1 are a feature of the inherited breast/ovarian cancer phenotype in selected families, Journal of Medical Genetics 2005, vol.42,(5),2005,pp e31-e34
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