User profiles for G. Chenevix-Trench

Georgia Chenevix-Trench

Queensland Institute of Medical Research
Verified email at qimr.edu.au
Cited by 77049

The OncoArray Consortium: a network for understanding the genetic architecture of common cancers

…, AC Antoniou, PDP Pharoah, G Chenevix-Trench… - … , biomarkers & prevention, 2017 - AACR
Background: Common cancers develop through a multistep process often including inherited
susceptibility. Collaboration among multiple institutions, and funding from multiple sources, …

Nevoid basal cell carcinoma syndrome: review of 118 affected individuals

…, C Wicking, G ChenevixTrench - American journal of …, 1994 - Wiley Online Library
… Diagnostic Criteria The diagnostic criteria were modifications of those used by Chenevix-Trench
et al. [19931. One member of each family was required to have two of four major …

Incessant ovulation, inflammation and epithelial ovarian carcinogenesis: revisiting old hypotheses

…, CR Beaugié, I Haviv, G Chenevix-Trench… - Molecular and cellular …, 2006 - Elsevier
Epithelial ovarian cancer (EOC) is often a lethal disease because in many cases early
symptoms go undetected. Although research proceeds apace, as yet there are few reliable and …

Mutations of the BRAF gene in human cancer

…, K Pritchard-Jones, N Maitland, G Chenevix-Trench… - Nature, 2002 - nature.com
… a, b, Conservation of amino acid sequence for the activation segment (a) and G loop (b). The
positions of mutations are indicated by yellow shading; V599 is denoted by an asterisk. The …

Patterns of somatic mutation in human cancer genomes

…, P Campbell, E Birney, DF Easton, G Chenevix-Trench… - Nature, 2007 - nature.com
Cancers arise owing to mutations in a subset of genes that confer growth advantage. The
availability of the human genome sequence led us to propose that systematic resequencing of …

Genome-wide association study identifies novel breast cancer susceptibility loci

…, S Seal, MR Stratton, N Rahman, G Chenevix-Trench… - Nature, 2007 - nature.com
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility
to the disease. Known susceptibility genes account for less than 25% of the familial risk of …

[HTML][HTML] Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

…, M Dean, R Toftgard, G Chenevix-Trench… - Cell, 1996 - cell.com
The nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder
characterized by multiple basal cell carcinomas (BCCs), pits of the palms and soles, jaw …

Intragenic ERBB2 kinase mutations in tumours

…, G Chenevix-Trench, BL Weber, ST Yuen, G Harris… - Nature, 2004 - nature.com
The protein-kinase family is the most frequently mutated gene family found in human cancer
and faulty kinase enzymes are being investigated as promising targets for the design of …

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies

…, H Holland, G Chenevix-Trench… - Journal of the …, 2011 - academic.oup.com
Background Previous studies have suggested that breast cancer risk factors are associated
with estrogen receptor (ER) and progesterone receptor (PR) expression status of the tumors. …

[HTML][HTML] Gene-panel sequencing and the prediction of breast-cancer risk

…, DGR Evans, G Chenevix-Trench… - … England Journal of …, 2015 - Mass Medical Soc
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk | NEJM Skip to main content
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