S. O’Connell

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Jane E. Carpenter, Jaana M. Hartikainen, W. Chung, 2019, Nature Genetics.

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Jane E. Carpenter, Jack A. Taylor, W. Chung, 2019, Nature Genetics.

Homologous recombination DNA repair defects in PALB2-associated breast cancers

I. Hickie, L. Lipton, A. Shelling, 2019, npj Breast Cancer.

A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome

Aung Ko Win, M. Clendenning, M. Wilding, 2023, Journal of Translational Medicine.

The impact of coding germline variants on contralateral breast cancer risk and survival

W. He, A. Børresen-Dale, N. Camp, 2023, American journal of human genetics.

TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members

Dale W. Garsed, Kenneth D. Doig, L. Andrews, 2022, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Jane E. Carpenter, W. Chung, M. Beckmann, 2019, npj Breast Cancer.

Homologous recombination DNA repair defects in PALB2-associated breast cancers

I. Hickie, L. Lipton, A. Shelling, 2019, npj Breast Cancer.

CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

Jane E. Carpenter, Jack A. Taylor, S. Cross, 2021, British Journal of Cancer.