Zosia Miedzybrodzka

Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.

Diana Eccles, Susan Peock, Rosemarie Davidson, 2013, Journal of the National Cancer Institute.

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Christiana Kartsonaki, Mads Thomassen, Etienne Rouleau, 2011, Human molecular genetics.

Parenting a child with clubfoot: A qualitative study

Edwin van Teijlingen, Simon Barker, Z. Miedzybrodzka, 2011 .

The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services

Diana M Eccles, Sue Thomas, Angela F Brady, 2014, Breast Cancer Research.

Cluster randomized trial of a multifaceted primary care decision-support intervention for inherited breast cancer risk.

Sarah Wordsworth, Adrian Grant, Jill Mollison, 2006, Family practice.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Germline mutations in RAD51D confer susceptibility to ovarian cancer

Deborah Hughes, Nazneen Rahman, Elise Ruark, 2011, Nature Genetics.

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

Peter Donnelly, Mark I. McCarthy, Nazneen Rahman, 2012, Nature.