Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: RENAL INSUFFICIENCY - GENETICS , . Treffer: 6
2022
Gorski, M; Rasheed, H; Teumer, A; Thomas, LF; Graham, SE; Sveinbjornsson, G; Winkler, TW; Günther, F; Stark, KJ; Chai, JF; Tayo, BO; Wuttke, M; Li, Y; Tin, A; Ahluwalia, TS; Ärnlöv, J; Åsvold, BO; Bakker, SJL; Banas, B; Bansal, N; Biggs, ML; Biino, G; Böhnke, M; Boerwinkle, E; Bottinger, EP; Brenner, H; Brumpton, B; Carroll, RJ; Chaker, L; Chalmers, J; Chee, ML; Chee, ML; Cheng, CY; Chu, AY; Ciullo, M; Cocca, M; Cook, JP; Coresh, J; Cusi, D; de, Borst, MH; Degenhardt, F; Eckardt, KU; Endlich, K; Evans, MK; Feitosa, MF; Franke, A; Freitag-Wolf, S; Fuchsberger, C; Gampawar, P; Gansevoort, RT; Ghanbari, M; Ghasemi, S; Giedraitis, V; Gieger, C; Gudbjartsson, DF; Hallan, S; Hamet, P; Hishida, A; Ho, K; Hofer, E; Holleczek, B; Holm, H; Hoppmann, A; Horn, K; Hutri-Kähönen, N; Hveem, K; Hwang, SJ; Ikram, MA; Josyula, NS; Jung, B; Kähönen, M; Karabegović, I; Khor, CC; Koenig, W; Kramer, H; Krämer, BK; Kühnel, B; Kuusisto, J; Laakso, M; Lange, LA; Lehtimäki, T; Li, M; Lieb, W; Lind, L; Lindgren, CM; Loos, RJF; Lukas, MA; Lyytikäinen, LP; Mahajan, A; Matias-Garcia, PR; Meisinger, C; Meitinger, T; Melander, O; Milaneschi, Y; Mishra, PP; Mononen, N; Morris, AP; Mychaleckyj, JC; Nadkarni, GN; Naito, M; Nakatochi, M; Nalls, MA; Nauck, M; Nikus, K; Ning, B; Nolte, IM; Nutile, T; O'Donoghue, ML; O'Connell, J; Olafsson, I; Orho-Melander, M; Parsa, A; Pendergrass, SA; Penninx, BWJH; Pirastu, M; Preuss, MH; Psaty, BM; Raffield, LM; Raitakari, OT; Rheinberger, M; Rice, KM; Rizzi, F; Rosenkranz, AR; Rossing, P; Rotter, JI; Ruggiero, D; Ryan, KA; Sabanayagam, C; Salvi, E; Schmidt, H; Schmidt, R; Scholz, M; Schöttker, B; Schulz, CA; Sedaghat, S; Shaffer, CM; Sieber, KB; Sim, X; Sims, M; Snieder, H; Stanzick, KJ; Thorsteinsdottir, U; Stocker, H; Strauch, K; Stringham, HM; Sulem, P; Szymczak, S; Taylor, KD; Thio, CHL; Tremblay, J; Vaccargiu, S; van, der, Harst, P; van, der, Most, PJ; Verweij, N; Völker, U; Wakai, K; Waldenberger, M; Wallentin, L; Wallner, S; Wang, J; Waterworth, DM; White, HD; Willer, CJ; Wong, TY; Woodward, M; Yang, Q; Yerges-Armstrong, LM; Zimmermann, M; Zonderman, AB; Bergler, T; Stefansson, K; Böger, CA; Pattaro, C; Köttgen, A; Kronenberg, F; Heid, IM, , Lifelines, Cohort, Study
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.
Kidney Int. 2022; 102(3): 624-639.
Doi: 10.1016/j.kint.2022.05.021
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2016
Alesutan, I; Feger, M; Tuffaha, R; Castor, T; Musculus, K; Buehling, SS; Heine, CL; Kuro-O, M; Pieske, B; Schmidt, K; Tomaschitz, A; Maerz, W; Pilz, S; Meinitzer, A; Voelkl, J; Lang, F
Augmentation of phosphate-induced osteo-/chondrogenic transformation of vascular smooth muscle cells by homoarginine.
Cardiovasc Res. 2016; 110(3):408-418
Doi: 10.1093/cvr/cvw062
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2015
Gorski, M; Tin, A; Garnaas, M; McMahon, GM; Chu, AY; Tayo, BO; Pattaro, C; Teumer, A; Chasman, DI; Chalmers, J; Hamet, P; Tremblay, J; Woodward, M; Aspelund, T; Eiriksdottir, G; Gudnason, V; Harris, TB; Launer, LJ; Smith, AV; Mitchell, BD; O'Connell, JR; Shuldiner, AR; Coresh, J; Li, M; Freudenberger, P; Hofer, E; Schmidt, H; Schmidt, R; Holliday, EG; Mitchell, P; Wang, JJ; de Boer, IH; Li, G; Siscovick, DS; Kutalik, Z; Corre, T; Vollenweider, P; Waeber, G; Gupta, J; Kanetsky, PA; Hwang, SJ; Olden, M; Yang, Q; de Andrade, M; Atkinson, EJ; Kardia, SL; Turner, ST; Stafford, JM; Ding, J; Liu, Y; Barlassina, C; Cusi, D; Salvi, E; Staessen, JA; Ridker, PM; Grallert, H; Meisinger, C; Müller-Nurasyid, M; Krämer, BK; Kramer, H; Rosas, SE; Nolte, IM; Penninx, BW; Snieder, H; Fabiola Del Greco, M; Franke, A; Nöthlings, U; Lieb, W; Bakker, SJ; Gansevoort, RT; van der Harst, P; Dehghan, A; Franco, OH; Hofman, A; Rivadeneira, F; Sedaghat, S; Uitterlinden, AG; Coassin, S; Haun, M; Kollerits, B; Kronenberg, F; Paulweber, B; Aumann, N; Endlich, K; Pietzner, M; Völker, U; Rettig, R; Chouraki, V; Helmer, C; Lambert, JC; Metzger, M; Stengel, B; Lehtimäki, T; Lyytikäinen, LP; Raitakari, O; Johnson, A; Parsa, A; Bochud, M; Heid, IM; Goessling, W; Köttgen, A; Kao, WH; Fox, CS; Böger, CA
Genome-wide association study of kidney function decline in individuals of European descent.
Kidney Int. 2015; 87(5):1017-1029
Doi: 10.1038/ki.2014.361
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2012
Krone, N; Reisch, N; Idkowiak, J; Dhir, V; Ivison, HE; Hughes, BA; Rose, IT; O'Neil, DM; Vijzelaar, R; Smith, MJ; MacDonald, F; Cole, TR; Adolphs, N; Barton, JS; Blair, EM; Braddock, SR; Collins, F; Cragun, DL; Dattani, MT; Day, R; Dougan, S; Feist, M; Gottschalk, ME; Gregory, JW; Haim, M; Harrison, R; Olney, AH; Hauffa, BP; Hindmarsh, PC; Hopkin, RJ; Jira, PE; Kempers, M; Kerstens, MN; Khalifa, MM; Köhler, B; Maiter, D; Nielsen, S; O'Riordan, SM; Roth, CL; Shane, KP; Silink, M; Stikkelbroeck, NM; Sweeney, E; Szarras-Czapnik, M; Waterson, JR; Williamson, L; Hartmann, MF; Taylor, NF; Wudy, SA; Malunowicz, EM; Shackleton, CH; Arlt, W
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.
J Clin Endocrinol Metab. 2012; 97(2):E257-E267
Doi: 10.1210/jc.2011-0640
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2011
Suhre, K; Shin, SY; Petersen, AK; Mohney, RP; Meredith, D; Wägele, B; Altmaier, E; CARDIoGRAM; Deloukas, P; Erdmann, J; Grundberg, E; Hammond, CJ; de Angelis, MH; Kastenmüller, G; Köttgen, A; Kronenberg, F; Mangino, M; Meisinger, C; Meitinger, T; Mewes, HW; Milburn, MV; Prehn, C; Raffler, J; Ried, JS; Römisch-Margl, W; Samani, NJ; Small, KS; Wichmann, HE; Zhai, G; Illig, T; Spector, TD; Adamski, J; Soranzo, N; Gieger, C; Assimes, TL; Deloukas, P; Erdmann, J; Holm, H; Kathiresan, S; König, IR; McPherson, R; Reilly, MP; Roberts, R; Samani, NJ; Schunkert, H; Stewart, AF
Human metabolic individuality in biomedical and pharmaceutical research.
Nature. 2011; 477(7362):54-60
Doi: 10.1038/nature10354
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2009
Kleinert, J; Kotanko, P; Spada, M; Pagliardini, S; Paschke, E; Paul, K; Voigtländer, T; Wallner, M; Kramar, R; Stummvoll, HK; Schwarz, C; Horn, S; Holzer, H; Födinger, M; Sunder-Plassmann, G
Anderson-Fabry disease: a case-finding study among male kidney transplant recipients in Austria.
Transpl Int. 2009; 22(3):287-292
Doi: 10.1111/j.1432-2277.2008.00791.x
(- Case Report)
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