Dr. rer. nat. Arif Bülent Ekici

Institute of Human Genetics

Biallelic SEMA3A defects cause a novel type of syndromic short stature (2013) Hofmann K, Zweier M, Sticht H, Zweier C, Wittmann W, Hoyer J, Uebe S, et al. Journal article Comparison of 6q25 breast cancer hits from Asian and European genome wide association studies in the Breast Cancer Association consortium (BCAC) (2012) Hein R, Maranian M, Hopper JL, Kapuscinski MK, Southey MC, Park DJ, Schmidt MK, et al. Journal article 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 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 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 CY, Weisschuh N, et al. Journal article