User profiles for Georgia Chenevix-Trench

Georgia Chenevix-Trench

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

Nevoid basal cell carcinoma syndrome: review of 118 affected individuals

…, C Wicking, G ChenevixTrench - American journal of …, 1994 - Wiley Online Library
One hundred eighteen cases of nevoid basal cell carcinoma syndrome (NBCCS, Gorlin's
syndrome or basal cell nevus syndrome) are presented in this study. In aiming to ascertain all …

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, …

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
Cancers arise owing to the accumulation of mutations in critical genes that alter normal
programmes of cell proliferation, differentiation and death. As the first stage of a systematic …

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

, … Adele 82 deFazio Anna 147 Chenevix-Trench Georgia … - 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 …

[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
NEJM Group Follow Us Facebook Twitter Instagram YouTube LinkedIn Prepare to become a …

Intragenic ERBB2 kinase mutations in tumours

…, B Malkowicz, MA Pierotti, B Teh, G Chenevix-Trench… - 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. …