Institute of Human Genetics

Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer (2015) O'Mara TA, Glubb DM, Painter JN, Cheng T, Dennis J, Attia J, Holliday EG, et al. Journal article Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression (2015) Darabi H, Mccue K, Beesley J, Michailidou K, Nord S, Kar S, Humphreys K, et al. Journal article Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1 (2015) Glubb DM, Maranian MJ, Michailidou K, Pooley KA, Meyer KB, Kar S, Carlebur S, et al. Journal article Prediction of breast cancer risk based on profiling with common genetic variants (2015) Mavaddat N, Pharoah PDP, Michailidou K, Tyrer J, Brook MN, Bolla MK, Wang Q, et al. Journal article Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk (2015) Amankwah EK, Lin HY, Tyrer JP, Lawrenson K, Dennis J, Chornokur G, Aben KKH, et al. Journal article Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium (2015) Johnatty SE, Tyrer JP, Kar S, Beesley J, Lu Y, Gao B, Fasching P, et al. Journal article Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer (2015) Couch FJ, Hart SN, Sharma P, Toland AE, Wang X, Miron P, Olson JE, et al. Journal article Endometriosis as a risk factor for ovarian or endometrial cancer - results of a hospital-based case-control study (2015) Burghaus S, Haeberle L, Schrauder MG, Heusinger K, Thiel F, Hein A, Wachter D, et al. Journal article A de novo microdeletion in NRXN1 in a Dutch patient with mild intellectual disability, microcephaly and gonadal dysgenesis (2015) Agha Z, Iqbal Z, Kleefstra T, Zweier C, Pfundt R, Qamar R, Van Bokhoven H, Willemsen MH Journal article Comprehensive screening for mutations associated with colorectal cancer in unselected cases reveals penetrant and nonpenetrant mutations (2015) Kraus C, Rau T, Lux P, Erlenbach-Wuensch K, Loehr S, Krumbiegel M, Thiel C, et al. Journal article