Dr. rer. nat. Arif Bülent Ekici

Institute of Human Genetics

Patients with unstable angina pectoris show an increased frequency of the Fc gamma RIIa R131 allele (2012) Raaz-Schrauder D, Ekici AB, Munoz LE, Klinghammer L, Voll RE, Leusen JH, Van De Winkel JG, et al. Journal article Genome-wide association study identifies a possible susceptibility locus for endometrial cancer (2012) Long J, Zheng W, Xiang YB, Lose F, Thompson D, Tomlinson I, Yu H, et al. Journal article Percent mammographic density and dense area as risk factors for breast cancer (2012) Rauh C, Hack C, Häberle L, Hein A, Engel A, Schrauder MG, Fasching P, et al. Journal article Genome-wide association analysis identifies three new breast cancer susceptibility loci (2012) Ghoussaini M, Fletcher O, Michailidou K, Turnbull C, Schmidt MK, Dicks E, Dennis J, et al. Journal article Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk (2011) Stevens KN, Garcia-Closas M, Fredericksen Z, Kosel M, Pankratz VS, Hopper JL, Dite GS, et al. Journal article Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: Findings from the Breast Cancer Association Consortium (2011) Broeks A, Schmidt MK, Sherman ME, Couch FJ, Hopper JL, Dite GS, Apicella C, et al. Journal article Breast cancer risk - Genes, environment and clinics Mammakarzinomrisiko - Gene, Umwelt und Klinik (2011) Fasching P, Ekici AB, Adamietz BR, Wachter DL, Hein A, Bayer CM, Häberle L, et al. Journal article Genome-wide association study identifies a common variant associated with risk of endometrial cancer (2011) Spurdle AB, Thompson DJ, Ahmed S, Ferguson K, Healey CS, O'Mara T, Walker LC, et al. Journal article Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: Pooled analysis within the ovarian cancer association consortium (2011) Lurie G, Wilkens LR, Thompson PJ, Shvetsov YB, Matsuno RK, Carney ME, Palmieri RT, et al. Journal article Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome (2011) Krumbiegel M, Pasutto F, Schlötzer-Schrehardt U, Uebe S, Zenkel M, Mardin C, Weisschuh N, et al. Journal article