E. Niedermayr

Improving mutation notification when new genetic information is identified in research: a trial of two strategies in familial breast cancer

J. Kirk, C. Wakefield, K. Tucker, 2012, Genetics in Medicine.

Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource

John L Hopper, Edward Edkins, Phyllis N Butow, 2006, Breast Cancer Research.

Monogenic and polygenic determinants of sarcoma risk: an international genetic study.

David M. Thomas, R. Sarin, J. Blay, 2016, The Lancet. Oncology.

The Dawn of a Revolution in Personalized Lung Cancer Prevention

S. Fox, J. Hopper, F. Khuri, 2011, Cancer Prevention Research.

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

Jaana M. Hartikainen, Kristen S Purrington, Ali Amin Al Olama, 2014, Human molecular genetics.

Heritable defects in telomere and mitotic function selectively predispose to sarcomas

Melissa J. Green, Emma M. Rath, R. Redon, 2023, Science.

A comparison of Australian and French families affected by sarcoma: perceptions of genetics and incidental findings.

David M. Thomas, J. Blay, I. Ray-Coquard, 2018, Personalized medicine.

Decreased Prostate Cancer-Specific Survival of Men with BRCA2 Mutations from Multiple Breast Cancer Families

H. Thorne, E. Niedermayr, D. Clouston, 2011, Cancer Prevention Research.