Cancer Genetics Laboratory

The Cancer Genetics Laboratory studies cancers of endocrine organs, many of which develop as a result of hereditary syndromes.

Our research team has expertise in cancer biology, diagnostic genetic testing, family counselling and targeted surveillance programs.

Our research translates discoveries in genetic research to improved clinical care for patients with endocrine cancers.


Lead

Professor Rory Clifton-Bligh A/Prof Roderick Clifton-Bligh


Head, Cancer Genetics Laboratory
Head, Department of Endocrinology, Royal North Shore Hospital

team-Bruce-Robinson Professor Bruce Robinson

Co-Head, Cancer Genetics Laboratory

Dr Stan Sidhu Professor Stan Sidhu

Co-Head, Cancer Genetics Laboratory

Dr Diana Benn Dr Diana (Dindy) Benn PhD

Senior Research Scientist

Dr Trisha Dwight Dr Trisha Dwight PhD

Research Fellow
Kolling Institute, Northern Clinical School

Dr Martyn Bullock Dr Martyn Bullock PhD

Scientific Officer | NSW Health Service
Senior Research Fellow | Northern Clinical School, University of Sydney
Visiting Scholar | University of Technology Sydney
Co-Chair |RNSH Institutional Biosafety Committee

Dr Catherine Luxford Dr Catherine Luxford PhD

Senior Scientific Officer NSW Health Service

Our current research programs are:

Cancer Genetics Diagnostic Laboratory

We perform NATA-accredited genetic testing for Multiple Endocrine Neoplasia syndrome type 2, Hereditary Phaeochromocytoma/Paraganglioma syndromes, hereditary hyperparathyroidism disorders and hereditary thyroid disorders.

Phaeochromocytoma/Paraganglioma syndromes

Studying hereditary mutations in key genes associated with phaeochromocytomas and paragangliomas. Our research has made several discoveries that link mitochondrial dysfunction with a predisposition to these and other cancers. These biomarker discoveries have been translated into routine pathology practice.

Thyroid Cancer

Studying tumour or hereditary DNA mutations that predispose people to thyroid cancers. Our ground breaking work has included discovery of fusion chromosomes in particular subtypes of thyroid cancer. It has also examined the role of the BRAF oncogene in cancer metastasis and the specific role of a thyroid developmental transcription factor FOXE1 with thyroid cancer predisposition, a finding that links disruption in an early developmental gene with cancer development in adult life.

Adrenal Cancer

In this program, we study the microRNA changes associated with the highly malignant cancer of the adrenal cortex.

Pituitary Tumours

Studying the genetic and epigenetic changes of pituitary neoplasms.

Events, News and Seminars

Cancer expertise recognised

Cancer expertise recognised

The Kolling’s Dr Amanda Hudson will lead an exciting pilot study after being awarded an innovation g..... Read more

Category: Funding support, Neuroscience and Pain Research

New funding launches exciting project to detect cancer earlier

New funding launches exciting project to detect cancer earlier

Congratulations to Kolling cancer researcher and Sydney Vital fellow Dr Yaser Hadi Gholami on being ..... Read more

Category: Funding support

Congratulations Professor Rob Baxter

Congratulations Professor Rob Baxter

Former Kolling Institute director Professor Rob Baxter received an Order of Australia medal in the Q..... Read more

Category: Awards