Institute of Human Genetics

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 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 (2015) Cheng THT, Thompson D, Painter J, O'Mara T, Gorman M, Martin L, Palles C, et al. Journal article MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and golgi architecture as a central mechanism in growth regulation (2015) Zahnleiter D, Hauer N, Keßler K, Uebe S, Sugano Y, Neuhauss SCF, Gießl A, et al. Journal article Inhibition of RAS activation due to a homozygous ezrin variant in patients with profound intellectual disability (2015) Riecken LB, Tawamie H, Dornblut C, Buchert R, Ismayel A, Schulz A, Schumacher J, et al. Journal article