Associate Investigators
Prof. Dr. Anna Köttgen
Kontakt
Prof. Dr. Anna Köttgen
Institute of Genetic Epidemiology
(University Medical Center Freiburg, Faculty of Medicine)
(University Medical Center Freiburg, Faculty of Medicine)
T +49 761 270 78050
anna.koettgen(at)uniklinik-freiburg.de
Weitere Informationen
10 selected publications
- Genetic Studies of Urinary Metabolites Illuminate Mechanisms of Detoxification and Excretion in Humans.
Schlosser P, Li Y, Sekula P, Raffler J, Grundner-Culemann F, Pietzner M, Cheng Y, Wuttke M, Steinbrenner I, Schultheiss UT, Kotsis F, Kacprowski T, Forer L, Hausknecht B, Ekici AB, Nauck M, Völker U; GCKD Investigators, Walz G, Oefner PJ, Kronenberg F, Mohney RP, Köttgen M, Suhre K, Eckardt KU, Kastenmüller G, Köttgen A (2020)
Nat Genet, 52(2):167-176 - Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
Tin A, Marten J, Halperin Kuhns VL, Li Y, Wuttke M, Kirsten H, …, Hung AM, Teumer A, Pattaro C, Woodward OM, Vitart V, Köttgen A (2019)
Nat Genet, 51(10):1459-1474 - Genome-wide association meta-analyses and fine-mapping elucidate novel pathways influencing albuminuria.
Teumer A, Li Y, Ghasemi S, Prins BP, Wuttke M, Hermle T, ..., Butterworth AS, Hung AM, Pattaro C, Köttgen A (2019)
Nat Commun, 10(1):4130 - A catalogue of genetic targets for kidney function from analyses of a million individuals.
Wuttke M, Li Y, Li M, Sieber KB, Feitosa MF, Gorski M, ..., Heid IM, Scholz M, Teumer A, Köttgen A*, Pattaro C* (2019)
Nat Genet, 51(6):957-972 - Epigenome-wide association studies identify DNA methylation associated with kidney function.
Chu AY, Tin A, Schlosser P, Ko YA, Qiu C, Yao C, Joehanes R, Grams ME, Liang L, Gluck CA, Liu C, Coresh J, Hwang SJ, Levy D, Boerwinkle E, Pankow JS, Yang Q, Fornage M, Fox CS, Susztak K, Köttgen A (2017)
Nat Commun, 8(1):1286 - Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, …, Caulfield M, Bochud M, Gieger C (2013)
Nat Genet 45(2):145-154 - Human metabolic individuality in biomedical and pharmaceutical research.
Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wagele B, Altmaier E, Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmuller G, Köttgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, Mewes HW, Milburn MV, Prehn C, Raffler J, Ried JS, Romisch-Margl W, Samani NJ, Small KS, Wichmann HE, Zhai G, Illig T, Spector TD, Adamski J, Soranzo N, Gieger C (2011)
Nature, 477(7362):54-60 - New loci associated with kidney function and chronic kidney disease.
Köttgen A, Pattaro C, Boger CA, Fuchsberger C, …, Kao WH, Heid IM, Fox CS (2010)
Nat Genet, 42(5):376-384 - Identification of a novel urate transporter, ABCG2, with a common functional polymorphism causing gout.
Woodward OM*, Köttgen A*, Coresh J, Boerwinkle E, Guggino WB, Köttgen M (2009)
Proc Natl Acad Sci U S A. 106(25):10338-42 - Multiple loci associated with indices of renal function and chronic kidney disease.
Köttgen A, Glazer NL, Dehghan A, Hwang SJ, …, Witteman JC, Coresh J, Shlipak MG, Fox CS (2009).
Nat Genet, 41(6):712-717