D-Index & Metrics Best Publications
Research.com 2022 Best Female Scientist Award Badge
Medicine
Australia
2023

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Best female scientists D-index 112 Citations 66,976 609 World Ranking 462 National Ranking 14
Medicine D-index 114 Citations 65,898 603 World Ranking 2670 National Ranking 83

Research.com Recognitions

Awards & Achievements

2023 - Research.com Medicine in Australia Leader Award

2022 - Research.com Best Female Scientist Award

2014 - Fellow of the Australian Academy of Science

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Cancer
  • Genetics

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.

Her most cited work include:

  • Mutations of the BRAF gene in human cancer (8295 citations)
  • Patterns of somatic mutation in human cancer genomes (2569 citations)
  • Genome-wide association study identifies novel breast cancer susceptibility loci (2077 citations)

What are the main themes of her work throughout her whole career to date?

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.

She most often published in these fields:

  • Breast cancer (52.12%)
  • Internal medicine (40.50%)
  • Genetics (39.40%)

What were the highlights of her more recent work (between 2016-2021)?

  • Breast cancer (52.12%)
  • Internal medicine (40.50%)
  • Oncology (36.26%)

In recent papers she was focusing on the following fields of study:

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.

Between 2016 and 2021, her most popular works were:

  • Association analysis identifies 65 new breast cancer risk loci (661 citations)
  • Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (335 citations)
  • Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (268 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Cancer
  • Mutation

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.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Mutations of the BRAF gene in human cancer

Helen Davies;Graham R. Bignell;Charles Cox;Philip Stephens.
Nature (2002)

11646 Citations

Patterns of somatic mutation in human cancer genomes

Christopher Greenman;Philip Stephens;Raffaella Smith;Gillian L. Dalgliesh.
Nature (2007)

3469 Citations

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)

2713 Citations

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)

2338 Citations

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)

1179 Citations

RAD51B in Familial Breast Cancer

Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski.
PLOS ONE (2016)

1014 Citations

Association analysis identifies 65 new breast cancer risk loci

Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Nature (2017)

969 Citations

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)

855 Citations

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)

836 Citations

Lung cancer: intragenic ERBB2 kinase mutations in tumours.

Philip Stephens;Chris Hunter;Graham Bignell;Sarah Edkins.
Nature (2004)

754 Citations

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