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.


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 of Medical Research, 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

New funding supports innovative approach to diagnose heart failure

New funding supports innovative approach to diagnose heart failure

Kolling researcher and Royal North Shore Hospital cardiologist Dr Rebecca Kozor will lead a world-fi..... Read more

Category: Funding support

Every week counts in the lead up to birth

Every week counts in the lead up to birth

The Kolling’s Women and Babies Research team is calling for a reduction in the number of early birth..... Read more

Category: Research Excellence

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