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Publication date
2019 06
Authors
Wuttke, M Li, Y Li, M Sieber, KB Feitosa, MF Gorski, M Tin, A Wang, LH Chu, AY Hoppmann, A Kirsten, H Giri, A Chai, JF Sveinbjornsson, G Tayo, BO Nutile, T Fuchsberger, C Marten, J Cocca, M Ghasemi, S Xu, YZ Horn, K Noce, D Van der Most, PJ Sedaghat, S Yu, Z Akiyama, M Afaq, S Ahluwalia, TS Almgren, P Amin, N Arnlo, J Bakker, SJL Bansal, N Baptista, D Bergmann, S Biggs, ML Biino, G Boehnke, M Boerwinkle, E Boissel, M Bottinger, EP Boutin, TS Brenner, H Brumat, M Burkhardt, R Butterworth, AS Butterworth, AS Campbell, A Campbell, H Canouil, M Carroll, RJ Catamo, E Chambers, JC Chee, ML Chee, ML Chen, X Cheng, CY Cheng, YR Christensen, K Cifkova, R Ciullo, M Concas, MP Cook, JP Coresh, J Corre, T Sala, CF Cusi, D Danesh, J Daw, EW Borst, MH Grandi, A Mutsert, R Vries, APJ Degenhardt, F Delgado, G Demirkan, A Di Angelantonio, E Dittrich, K Divers, J Dorajoo, R Eckardt, KU Ehret, G Elliott, P Endlich, K Evans, MK Felix, JF Foo, VHX Franco, OH Franke, A Freedman, BI Freitag-Wolf, S Friedlander, Y Froguel, P Gansevoort, RT Gao, H Gasparini, P Gaziano, JM Giedraitis, V Gieger, C Girotto, G Giulianini, F Gogele, M Gordon, SD Gudbjartsson, DF Gudnason, V Haller, T Hamet, P Harris, TB Hartman, CA Hayward, C Hellwege, JN Heng, CK Hicks, AA Hofer, E Huang, W Hutri-Kahonen, N Hwang, SJ Ikram, MA Indridason, OS Ingelsson, E Ising, M Jaddoe, VWV Jakobsdottir, J Jonas, JB Joshi, PK Josyula, NS Jung, B Kahonen, M Kamatani, Y Kammerer, CM Kanai, M Kastarinen, M Kerr, SM Khor, CC Kiess, W Kleber, ME Koenig, W Kooner, JS Korner, A Kovacs, P Kraja, AT Krajcoviechova, A Kramer, H Kramer, BK Kronenberg, F Kubo, M Kuhnel, B Kuokkanen, M Kuusisto, J Bianca, M Laakso, M Lange, LA Langefeld, CD Lee, JJM Lehne, B Lehtimaki, T Lieb, W Lim, SC Lind, L Lindgren, CM Liu, J Liu, JJ Loeffler, M Loos, RJF Lucae, S Lukas, MA Lyytikainen, LP Magi, R Magnusson, PKE Mahajan, A Martin, NG Martins, J Marz, W Mascalzoni, D Matsuda, K Meisinger, C Meitinger, T Melander, O Metspalu, A Mikaelsdottir, EK Milaneschi, Y Miliku, K Mishra, PP Program, VAMV Mohlke, KL Mononen, N Montgomery, GW Mook-Kanamori, DO Mychaleckyj, JC Nadkarni, GN Nalls, MA Nauck, M Nikus, K Ning, B Nolte, IM Noordam, R O'Connell, J O'Donoghue, ML Olafsson, I Oldehinkel, AJ Orho-Melander, M Ouwehand, WH Padmanabhan, S Palmer, ND Palsson, R Penninx, BWJH Perls, T Perola, M Pirastu, M Pirastu, N Pistis, G Podgornaia, AI Polasek, O Ponte, B Porteous, DJ Poulain, T Pramstaller, PP Preuss, MH Prins, BP Province, MA Rabelink, TJ Raffield, LM Raitakari, OT Reilly, DF Rettig, R Rheinberger, M Rice, KM Ridker, PM Rivadeneira, F Rizzi, F Roberts, DJ Robino, A Rossing, P Rudan, I Rueedi, R Ruggiero, D Ryan, KA Saba, Y Sabanayagam, C Salomaa, V Salvi, E Saum, KU Schmidt, H Schmidt, R Schottker, Schulz, CA Schupf, N Shaffer, CM Shi, Y Smith, AV Smith, BH Soranzo, N Spracklen, CN Strauch, K Stringham, HM Stumvoll, M Svensson, PO Szymczak, S Tai, ES Tajuddin, SM Tan, NYQ Taylor, KD Teren, A Tham, YC Thiery, J Thio, CHL Thomsen, H Thorleifsson, G Toniolo, D Tonjes, A Tremblay, J Tzoulaki, I Uitterlinden, AG Vaccargiu, S Van Dam, RM Harst, PD Duijn, CM Edward, DRV Verweij, N Vogelezang, S Volker, U Vollenweider, P Waeber, G Waldenberger, M Wallentin, L Wang, YX Wang, C Waterworth, DM Wei, W White, H Whitfield, JB Wild, SH Wilson, JF Wojczynski, MK Wong, C Wong, TY Xu, L Yang, Q Yasuda, M Yerges-Armstrong, LM Zhang, WH Zonderman, AB Rotter, JI Bochud, M Psaty, BM Vitart, V Wilson, JG Dehghan, A Parsa, A Chasman, DI Ho, K Morris, AP Devuyst, O Akilesh, S Pendergrass, SA Sim, XL Boger, CA Okada, Y Edwards, TL Snieder, H Stefansson, K Hung, AM Heid, IM Scholz, M Teumer, A Kottgen, A Pattaro, C
Group authors
Lifelines COHort Study
Author KI Usernames
Magnusson, PKE|patmag Svensson, PO|psvenss
Pubmed ID
31152163
Journal
Nature genetics
Doctype
Article
KI Connection
Låg
Mesh SV
Fenotyp Genetiska sjukdomsanlag Genetisk associationsundersökning Genkartläggning Genome-Wide Association Study Glomerulär filtrationshastighet Kronisk njurfunktionsförsämring Människa Njurfunktionstester Polymorfism, enkelnukleotid QTL Urbefolkningen i Europa Uromodulin Ärftliga mönster Ärftlig kvantitativ egenskap
Mesh EN
Chromosome Mapping European Continental Ancestry Group Genetic Association Studies Genetic Predisposition to Disease Genome-Wide Association Study Glomerular Filtration Rate Inheritance Patterns Kidney Function Tests Phenotype Polymorphism, Single Nucleotide Quantitative Trait, Heritable Quantitative Trait Loci Renal Insufficiency, Chronic Uromodulin
First date
2019-06-30T03:40:33.581Z