2023 - Research.com Medicine in Australia Leader Award
2022 - Research.com Best Female Scientist Award
2014 - Fellow of the Australian Academy of Science
Georgia Chenevix-Trench mostly deals with Breast cancer, Genetics, Genome-wide association study, Cancer and Internal medicine. Her studies in Breast cancer integrate themes in fields like Odds ratio, TOX3, Genetic predisposition and Genotype. Her research links Cancer research with Genetics.
Her study on Genome-wide association study is covered under Single-nucleotide polymorphism. Her research in Cancer focuses on subjects like Germline mutation, which are connected to Germline. Her Internal medicine research includes themes of Endocrinology, Gynecology and Oncology.
Georgia Chenevix-Trench spends much of her time researching Breast cancer, Internal medicine, Genetics, Oncology and Ovarian cancer. Her work carried out in the field of Breast cancer brings together such families of science as Cancer research and Genome-wide association study, Genotype, Single-nucleotide polymorphism. Her Genome-wide association study research is multidisciplinary, incorporating perspectives in Genetic predisposition, Bioinformatics, Expression quantitative trait loci, Genotyping and Genetic association.
She has included themes like Endocrinology and Gynecology in her Internal medicine study. Her Oncology research includes elements of Hazard ratio, Confidence interval, Proportional hazards model, Penetrance and Risk factor. Georgia Chenevix-Trench interconnects Carcinoma, Serous fluid, Germline and Candidate gene in the investigation of issues within Ovarian cancer.
Her primary areas of study are Breast cancer, Internal medicine, Oncology, Genome-wide association study and Genetics. Her Breast cancer research is classified as research in Cancer. Her Internal medicine study frequently links to other fields, such as Single-nucleotide polymorphism.
Georgia Chenevix-Trench has researched Oncology in several fields, including Cohort study, Serous fluid, Case-control study, Ovarian cancer and Prostate cancer. The Ovarian cancer study combines topics in areas such as Carcinoma, Disease, Genotype and Candidate gene. Her Genome-wide association study research integrates issues from Transcriptome, Medical genetics, Genetic predisposition and Expression quantitative trait loci.
Her primary areas of investigation include Breast cancer, Internal medicine, Oncology, Genome-wide association study and Genetics. Her Breast cancer research is multidisciplinary, relying on both Single-nucleotide polymorphism, Case-control study and Ovarian cancer. Her study in Ovarian cancer is interdisciplinary in nature, drawing from both Serous fluid, Survival analysis and Cancer research.
Her research in Internal medicine intersects with topics in Gynecology and Gene mutation. Her Genome-wide association study research incorporates elements of Genetic predisposition, Genetic model, Transcriptome, Medical genetics and Genetic variation. The various areas that Georgia Chenevix-Trench examines in her Cancer study include Germline mutation and Bioinformatics.
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Mutations of the BRAF gene in human cancer
Helen Davies;Graham R. Bignell;Charles Cox;Philip Stephens.
Nature (2002)
Patterns of somatic mutation in human cancer genomes
Christopher Greenman;Philip Stephens;Raffaella Smith;Gillian L. Dalgliesh.
Nature (2007)
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton;Karen A. Pooley;Alison M. Dunning;Paul D. P. Pharoah.
Nature (2007)
Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome
Heidi Hahn;Carol Wicking;Peter G Zaphiropoulos;Mae R Gailani.
Cell (1996)
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)
RAD51B in Familial Breast Cancer
Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski.
PLOS ONE (2016)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Nature (2017)
Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies
Xiaohong R. Yang;Jenny Chang-Claude;Ellen L. Goode;Fergus J. Couch.
Journal of the National Cancer Institute (2011)
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
Douglas Frederick Easton;Paul David Pharoah;Antonis C. Antoniou;Marc Derek Tischkowitz.
The New England Journal of Medicine (2015)
Lung cancer: intragenic ERBB2 kinase mutations in tumours.
Philip Stephens;Chris Hunter;Graham Bignell;Sarah Edkins.
Nature (2004)
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