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Pigment Cell & Melanoma Research|November 29, 2014
Genetics of familial melanoma: 20 years after CDKN2ALauren G Aoude, Karin A W Wadt, Antonia L Pritchard, et al.
Trends in Genetics : TIG|July 10, 2022
Unusual suspects in hereditary melanoma: POT1, POLE, BAP1Ellie J Maas, Brigid Betz-Stablein, Lauren G Aoude, et al.
Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society|February 14, 2026
Agent-MIRA: AI-orchestrated medical imaging agent for PET image retrieval and assistanceRajat Vashistha, Sandra Brosda, Lauren G Aoude, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|March 20, 2015
Prevalence of Germline BAP1, CDKN2A, and CDK4 Mutations in an Australian Population-Based Sample of Cutaneous Melanoma CasesLauren G Aoude, Michael Gartside, Peter Johansson, et al.
Familial Cancer|January 21, 2015
Germline RAD51B truncating mutation in a family with cutaneous melanomaKarin A W Wadt, Lauren G Aoude, Lisa Golmard, et al.
Plos One|August 27, 2013
A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancersLauren G Aoude, Karin Wadt, Anders Bojesen, et al.
Pigment Cell & Melanoma Research|March 26, 2011
Melanoma cell invasiveness is regulated by miR-211 suppression of the BRN2 transcription factorGlen M Boyle, Susan L Woods, Vanessa F Bonazzi, et al.
Cancer Research|August 6, 2013
SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesisJulia C Cronin, Dawn E Watkins-Chow, Art Incao, et al.
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