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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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Target genes, variants, tissues and transcriptional pathways influencing human serum urate levelsA. Tin, J. Marten, V. Halperin Kuhns, Y. Li, M. Wuttke, H. Kirsten, K. Sieber, C. Qiu, M. Gorski, Z. Yu and 218 other author(s). Nat. Genet., 51 (10): 1459--1474 (October 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)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)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)Common variants in the CLDN2-MORC4 and PRSS1-PRSS2 loci confer susceptibility to acute pancreatitisF. Weiss, N. Hesselbarth, A. Párniczky, D. Mosztbacher, F. Lämmerhirt, C. Ruffert, P. Kovacs, S. Beer, K. Seltsam, H. Griesmann and 22 other author(s). Pancreatology, 18 (5): 477--481 (July 2018)

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Disambiguation of "Kovacs, Peter"

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

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Disambiguation of "Kovacs, Peter"

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