Dr. rer. nat. Arif Bülent Ekici

Institute of Human Genetics

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy (2015) Lei J, Rudolph A, Moysich KB, Rafiq S, Behrens S, Goode EL, Pharoah PP, et al. Journal article Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk (2015) Kar SP, Tyrer JP, Li Q, Lawrenson K, Aben KKH, Anton-Culver H, Antonenkova N, et al. Journal article Identification of six new susceptibility loci for invasive epithelial ovarian cancer (2015) Kuchenbaecker KB, Ramus SJ, Tyrer J, Lee A, Shen HC, Beesley J, Lawrenson K, et al. Journal article Common germline polymorphisms associated with breast cancer-specific survival (2015) Pirie A, Guo Q, Kraft P, Canisius S, Eccles DM, Rahman N, Nevanlinna H, et al. Journal article Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases (2015) Moosmann J, Uebe S, Dittrich S, Rueffer A, Ekici AB, Toka O Journal article Do telomeres have a higher plasticity than thought? Results from the German Chronic Kidney Disease (GCKD) study as a high-risk population (2015) Raschenberger J, Kollerits B, Titze S, Koettgen A, Bärthlein B, Ekici AB, Forer L, et al. Journal article Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma (2015) Pasutto F, Mauri L, Popp B, Sticht H, Ekici AB, Piozzi E, Bonfante A, et al. Journal article Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk (2015) Lin WY, Camp NJ, Ghoussaini M, Beesley J, Michailidou K, Hopper JL, Apicella C, et al. Journal article Large-scale evaluation of common variation in regulatory T cell-related genes and ovarian cancer outcome (2014) Charbonneau B, Moysich KB, Kalli KR, Oberg AL, Vierkant RA, Fogarty ZC, Block MS, et al. Journal article A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency (2014) Buchert R, Tawamie H, Smith C, Uebe S, Innes AM, Al Hallak B, Ekici AB, et al. Journal article