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Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

A. Tin, J. Marten, V. Halperin Kuhns, Y. Li, M. Wuttke, H. Kirsten, K. Sieber, C. Qiu, M. Gorski, Z. Yu, A. Giri, G. Sveinbjornsson, M. Li, A. Chu, A. Hoppmann, L. O'Connor, B. Prins, T. Nutile, D. Noce, M. Akiyama, M. Cocca, S. Ghasemi, P. van der Most, K. Horn, Y. Xu, C. Fuchsberger, S. Sedaghat, S. Afaq, N. Amin, J. Ärnlöv, S. Bakker, N. Bansal, D. Baptista, S. Bergmann, M. Biggs, G. Biino, E. Boerwinkle, E. Bottinger, T. Boutin, M. Brumat, R. Burkhardt, E. Campana, A. Campbell, H. Campbell, R. Carroll, E. Catamo, J. Chambers, M. Ciullo, M. Concas, J. Coresh, T. Corre, D. Cusi, S. Felicita, M. de Borst, A. De Grandi, R. de Mutsert, A. de Vries, G. Delgado, A. Demirkan, O. Devuyst, K. Dittrich, K. Eckardt, G. Ehret, K. Endlich, M. Evans, R. Gansevoort, P. Gasparini, V. Giedraitis, C. Gieger, G. Girotto, M. Gögele, S. Gordon, D. Gudbjartsson, V. Gudnason, German Chronic Kidney Disease Study, T. Haller, P. Hamet, T. Harris, C. Hayward, A. Hicks, E. Hofer, H. Holm, W. Huang, N. Hutri-Kähönen, S. Hwang, M. Ikram, R. Lewis, E. Ingelsson, J. Jakobsdottir, I. Jonsdottir, H. Jonsson, P. Joshi, N. Josyula, B. Jung, M. Kähönen, Y. Kamatani, M. Kanai, S. Kerr, W. Kiess, M. Kleber, W. Koenig, J. Kooner, A. Körner, P. Kovacs, B. Krämer, F. Kronenberg, M. Kubo, B. Kühnel, M. La Bianca, L. Lange, B. Lehne, T. Lehtimäki, Lifelines Cohort Study, J. Liu, M. Loeffler, R. Loos, L. Lyytikäinen, R. Magi, A. Mahajan, N. Martin, W. März, D. Mascalzoni, K. Matsuda, C. Meisinger, T. Meitinger, A. Metspalu, Y. Milaneschi, V. A. Million Veteran Program, C. O'Donnell, O. Wilson, J. Gaziano, P. Mishra, K. Mohlke, N. Mononen, G. Montgomery, D. Mook-Kanamori, M. Müller-Nurasyid, G. Nadkarni, M. Nalls, M. Nauck, K. Nikus, B. Ning, I. Nolte, R. Noordam, J. O'Connell, I. Olafsson, S. Padmanabhan, B. Penninx, T. Perls, A. Peters, M. Pirastu, N. Pirastu, G. Pistis, O. Polasek, B. Ponte, D. Porteous, T. Poulain, M. Preuss, T. Rabelink, L. Raffield, O. Raitakari, R. Rettig, M. Rheinberger, K. Rice, F. Rizzi, A. Robino, I. Rudan, A. Krajcoviechova, R. Cifkova, R. Rueedi, D. Ruggiero, K. Ryan, Y. Saba, E. Salvi, H. Schmidt, R. Schmidt, C. Shaffer, A. Smith, B. Smith, C. Spracklen, K. Strauch, M. Stumvoll, P. Sulem, S. Tajuddin, A. Teren, J. Thiery, C. Thio, U. Thorsteinsdottir, D. Toniolo, A. Tönjes, J. Tremblay, A. Uitterlinden, S. Vaccargiu, P. van der Harst, C. van Duijn, N. Verweij, U. Völker, P. Vollenweider, G. Waeber, M. Waldenberger, J. Whitfield, S. Wild, J. Wilson, Q. Yang, W. Zhang, A. Zonderman, M. Bochud, J. Wilson, S. Pendergrass, K. Ho, A. Parsa, P. Pramstaller, B. Psaty, C. Böger, H. Snieder, A. Butterworth, Y. Okada, T. Edwards, K. Stefansson, K. Susztak, M. Scholz, I. Heid, A. Hung, A. Teumer, C. Pattaro, O. Woodward, V. Vitart, and A. Köttgen. Nat. Genet., 51 (10): 1459--1474 (October 2019)

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Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery diseaseJ. Pott, Y. Bae, K. Horn, A. Teren, A. Kühnapfel, H. Kirsten, U. Ceglarek, M. Loeffler, J. Thiery, J. Kratzsch and 1 other author(s). J. Clin. Endocrinol. Metab., 104 (11): 5008--5023 (November 2019)Meta-analysis uncovers genome-wide significant variants for rapid kidney function declineM. Gorski, B. Jung, Y. Li, P. Matias-Garcia, M. Wuttke, S. Coassin, C. Thio, M. Kleber, T. Winkler, V. Wanner and 123 other author(s). Kidney Int., 99 (4): 926--939 (April 2021)Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced diseaseT. Winkler, F. Grassmann, C. Brandl, C. Kiel, F. Günther, T. Strunz, L. Weidner, M. Zimmermann, C. Korb, A. Poplawski and 15 other author(s). BMC Med. Genomics, 13 (1): 120 (August 2020)A catalog of genetic loci associated with kidney function from analyses of a million individualsM. Wuttke, Y. Li, M. Li, K. Sieber, M. Feitosa, M. Gorski, A. Tin, L. Wang, A. Chu, A. Hoppmann and 319 other author(s). Nat. Genet., 51 (6): 957--972 (June 2019)HLA class II allele analyses implicate common genetic components in type 1 and non-insulin-treated type 2 diabetesT. Jacobi, L. Massier, N. Klöting, K. Horn, A. Schuch, P. Ahnert, C. Engel, M. Löffler, R. Burkhardt, J. Thiery and 6 other author(s). J. Clin. Endocrinol. Metab., 105 (3): e245--e254 (March 2020)Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaA. Teumer, Y. Li, S. Ghasemi, B. Prins, M. Wuttke, T. Hermle, A. Giri, K. Sieber, C. Qiu, H. Kirsten and 176 other author(s). Nat. Commun., 10 (1): 4130 (September 2019)Meta-analysis uncovers genome-wide significant variants for rapid kidney function declineM. Gorski, B. Jung, Y. Li, P. Matias-Garcia, M. Wuttke, S. Coassin, C. Thio, M. Kleber, T. Winkler, V. Wanner and 169 other author(s). Kidney International, 99 (4): 926--939 (2021)Circulating oxytocin is genetically determined and associated with obesity and impaired glucose toleranceM. Weingarten, M. Scholz, T. Wohland, K. Horn, M. Stumvoll, P. Kovacs, and A. Tönjes. J. Clin. Endocrinol. Metab., 104 (11): 5621--5632 (November 2019)Genome-wide analysis of carotid plaque burden suggests a role of IL5 in menJ. Pott, F. Beutner, K. Horn, H. Kirsten, K. Olischer, K. Wirkner, M. Loeffler, and M. Scholz. PLoS One, 15 (5): e0233728 (May 2020)Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressureM. Rode, A. Teren, K. Wirkner, K. Horn, H. Kirsten, M. Loeffler, M. Scholz, and J. Pott. PLoS One, 15 (8): e0237237 (August 2020)

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Disambiguation of "Horn, Katrin"

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Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

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Disambiguation of "Horn, Katrin"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

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Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels