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Items where Author is "Meitinger, T."

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Number of items: 4.

2020

Fawcett, K. A. and Obeidat, M. and Melbourne, C. and Shrine, N. and Guyatt, A. L. and John, C. and Luan, J. and Richmond, A. and Moksnes, M. R. and Granell, R. and Weiss, S. and Imboden, M. and May-Wilson, S. and Hysi, P. and Boutin, T. S. and Portas, L. and Flexeder, C. and Harris, S. E. and Wang, C. A. and Lyytikainen, L. P. and Palviainen, T. and Foong, R. E. and Keidel, D. and Minelli, C. and Langenberg, C. and Bosse, Y. and Van den Berge, M. and Sin, D. D. and Hao, K. and Campbell, A. and Porteous, D. and Padmanabhan, S. and Smith, B. H. and Evans, D. M. and Ring, S. and Langhammer, A. and Hveem, K. and Willer, C. and Ewert, R. and Stubbe, B. and Pirastu, N. and Klaric, L. and Joshi, P. K. and Patasova, K. and Massimo, M. and Polasek, O. and Starr, J. M. and Karrasch, S. and Strauch, K. and Meitinger, T. and Rudan, I. and Rantanen, T. and Pietilainen, K. and Kahonen, M. and Raitakari, O. T. and Hall, G. L. and Sly, P. D. and Pennell, C. E. and Kaprio, J. and Lehtimaki, T. and Vitart, V. and Deary, I. J. and Jarvis, D. and Wilson, J. F. and Spector, T. and Probst-Hensch, N. and Wareham, N. J. and Volzke, H. and Henderson, J. and Strachan, D. P. and Brumpton, B. M. and Hayward, C. and Hall, I. P. and Tobin, M. D. and Wain, L. V.. (2020) Variants associated with; HHIP; expression have sex-differential effects on lung function. Wellcome Open Res, 5. p. 111.

2016

van Rheenen, W. and Shatunov, A. and Dekker, A. M. and McLaughlin, R. L. and Diekstra, F. P. and Pulit, S. L. and van der Spek, R. A. and Vosa, U. and de Jong, S. and Robinson, M. R. and Yang, J. and Fogh, I. and van Doormaal, P. T. and Tazelaar, G. H. and Koppers, M. and Blokhuis, A. M. and Sproviero, W. and Jones, A. R. and Kenna, K. P. and van Eijk, K. R. and Harschnitz, O. and Schellevis, R. D. and Brands, W. J. and Medic, J. and Menelaou, A. and Vajda, A. and Ticozzi, N. and Lin, K. and Rogelj, B. and Vrabec, K. and Ravnik-Glavac, M. and Koritnik, B. and Zidar, J. and Leonardis, L. and Groselj, L. D. and Millecamps, S. and Salachas, F. and Meininger, V. and de Carvalho, M. and Pinto, S. and Mora, J. S. and Rojas-Garcia, R. and Polak, M. and Chandran, S. and Colville, S. and Swingler, R. and Morrison, K. E. and Shaw, P. J. and Hardy, J. and Orrell, R. W. and Pittman, A. and Sidle, K. and Fratta, P. and Malaspina, A. and Topp, S. and Petri, S. and Abdulla, S. and Drepper, C. and Sendtner, M. and Meyer, T. and Ophoff, R. A. and Staats, K. A. and Wiedau-Pazos, M. and Lomen-Hoerth, C. and Van Deerlin, V. M. and Trojanowski, J. Q. and Elman, L. and McCluskey, L. and Basak, A. N. and Tunca, C. and Hamzeiy, H. and Parman, Y. and Meitinger, T. and Lichtner, P. and Radivojkov-Blagojevic, M. and Andres, C. R. and Maurel, C. and Bensimon, G. and Landwehrmeyer, B. and Brice, A. and Payan, C. A. and Saker-Delye, S. and Durr, A. and Wood, N. W. and Tittmann, L. and Lieb, W. and Franke, A. and Rietschel, M. and Cichon, S. and Nothen, M. M. and Amouyel, P. and Tzourio, C. and Dartigues, J. F. and Uitterlinden, A. G. and Rivadeneira, F. and Estrada, K. and Hofman, A. and Curtis, C. and Blauw, H. M. and van der Kooi, A. J. and de Visser, M. and Goris, A. and Weber, M. and Shaw, C. E. and Smith, B. N. and Pansarasa, O. and Cereda, C. and Del Bo, R. and Comi, G. P. and D'Alfonso, S. and Bertolin, C. and Soraru, G. and Mazzini, L. and Pensato, V. and Gellera, C. and Tiloca, C. and Ratti, A. and Calvo, A. and Moglia, C. and Brunetti, M. and Arcuti, S. and Capozzo, R. and Zecca, C. and Lunetta, C. and Penco, S. and Riva, N. and Padovani, A. and Filosto, M. and Muller, B. and Stuit, R. J. and Parals Registry, and Slalom Group, and Slap Registry, and Fals Sequencing Consortium, and Slagen Consortium, and Nnipps Study Group, and Blair, I. and Zhang, K. and McCann, E. P. and Fifita, J. A. and Nicholson, G. A. and Rowe, D. B. and Pamphlett, R. and Kiernan, M. C. and Grosskreutz, J. and Witte, O. W. and Ringer, T. and Prell, T. and Stubendorff, B. and Kurth, I. and Hubner, C. A. and Leigh, P. N. and Casale, F. and Chio, A. and Beghi, E. and Pupillo, E. and Tortelli, R. and Logroscino, G. and Powell, J. and Ludolph, A. C. and Weishaupt, J. H. and Robberecht, W. and Van Damme, P. and Franke, L. and Pers, T. H. and Brown, R. H. and Glass, J. D. and Landers, J. E. and Hardiman, O. and Andersen, P. M. and Corcia, P. and Vourc'h, P. and Silani, V. and Wray, N. R. and Visscher, P. M. and de Bakker, P. I. and van Es, M. A. and Pasterkamp, R. J. and Lewis, C. M. and Breen, G. and Al-Chalabi, A. and van den Berg, L. H. and Veldink, J. H.. (2016) Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nature Genetics, 48 (9). pp. 1043-1048.

2014

Arking, D. E. and Pulit, S. L. and Crotti, L. and van der Harst, P. and Munroe, P. B. and Koopmann, T. T. and Sotoodehnia, N. and Rossin, E. J. and Morley, M. and Wang, X. and Johnson, A. D. and Lundby, A. and Gudbjartsson, D. F. and Noseworthy, P. A. and Eijgelsheim, M. and Bradford, Y. and Tarasov, K. V. and Dörr, M. and Müller-Nurasyid, M. and Lahtinen, A. M. and Nolte, I. M. and Smith, A. V. and Bis, J. C. and Isaacs, A. and Newhouse, S. J. and Evans, D. S. and Post, W. S. and Waggott, D. and Lyytikäinen, L. P. and Hicks, A. A. and Eisele, L. and Ellinghaus, D. and Hayward, C. and Navarro, P. and Ulivi, S. and Tanaka, T. and Tester, D. J. and Chatel, S. and Gustafsson, S. and Kumari, M. and Morris, R. W. and Naluai, ÅT and Padmanabhan, S. and Kluttig, A. and Strohmer, B. and Panayiotou, A. G. and Torres, M. and Knoflach, M. and Hubacek, J. A. and Slowikowski, K. and Raychaudhuri, S. and Kumar, R. D. and Harris, T. B. and Launer, L. J. and Shuldiner, A. R. and Alonso, A. and Bader, J. S. and Ehret, G. and Huang, H. and Kao, W. H. and Strait, J. B. and Macfarlane, P. W. and Brown, M. and Caulfield, M. J. and Samani, N. J. and Kronenberg, F. and Willeit, J. and CARe Consortium, and Cogent Consortium, and Smith, J. G. and Greiser, K. H. and Meyer zu Schwabedissen, H. and Werdan, K. and Carella, M. and Zelante, L. and Heckbert, S. R. and Psaty, B. M. and Rotter, J. I. and Kolcic, I. and Polašek, O. and Wright, A. F. and Griffin, M. and Daly, M. J. and Dcct/Edic, and Arnar, D. O. and Hólm, H. and Thorsteinsdottir, U. and eMerge Consortium, and Denny, J. C. and Roden, D. M. and Zuvich, R. L. and Emilsson, V. and Plump, A. S. and Larson, M. G. and O'Donnell, C. J. and Yin, X. and Bobbo, M. and D'Adamo, A. P. and Iorio, A. and Sinagra, G. and Carracedo, A. and Cummings, S. R. and Nalls, M. A. and Jula, A. and Kontula, K. K. and Marjamaa, A. and Oikarinen, L. and Perola, M. and Porthan, K. and Erbel, R. and Hoffmann, P. and Jöckel, K. H. and Kälsch, H. and Nöthen, M. M. and Hrgen Consortium, and den Hoed, M. and Loos, R. J. and Thelle, D. S. and Gieger, C. and Meitinger, T. and Perz, S. and Peters, A. and Prucha, H. and Sinner, M. F. and Waldenberger, M. and de Boer, R. A. and Franke, L. and van der Vleuten, P. A. and Beckmann, B. M. and Martens, E. and Bardai, A. and Hofman, N. and Wilde, A. A. and Behr, E. R. and Dalageorgou, C. and Giudicessi, J. R. and Medeiros-Domingo, A. and Barc, J. and Kyndt, F. and Probst, V. and Ghidoni, A. and Insolia, R. and Hamilton, R. M. and Scherer, S. W. and Brandimarto, J. and Margulies, K. and Moravec, C. E. and del Greco, M. F. and Fuchsberger, C. and O'Connell, J. R. and Lee, W. K. and Watt, G. C. and Campbell, H. and Wild, S. H. and El Mokhtari, N. E. and Frey, N. and Asselbergs, F. W. and Mateo Leach, I. and Navis, G. and van den Berg, M. P. and van Veldhuisen, D. J. and Kellis, M. and Krijthe, B. P. and Franco, O. H. and Hofman, A. and Kors, J. A. and Uitterlinden, A. G. and Witteman, J. C. and Kedenko, L. and Lamina, C. and Oostra, B. A. and Abecasis, G. R. and Lakatta, E. G. and Mulas, A. and Orrú, M. and Schlessinger, D. and Uda, M. and Markus, M. R. and Völker, U. and Snieder, H. and Spector, T. D. and Ärnlöv, J. and Lind, L. and Sundström, J. and Syvänen, A. C. and Kivimaki, M. and Kähönen, M. and Mononen, N. and Raitakari, O. T. and Viikari, J. S. and Adamkova, V. and Kiechl, S. and Brion, M. and Nicolaides, A. N. and Paulweber, B. and Haerting, J. and Dominiczak, A. F. and Nyberg, F. and Whincup, P. H. and Hingorani, A. D. and Schott, J. J. and Bezzina, C. R. and Ingelsson, E. and Ferrucci, L. and Gasparini, P. and Wilson, J. F. and Rudan, I. and Franke, A. and Mühleisen, T. W. and Pramstaller, P. P. and Lehtimäki, T. J. and Paterson, A. D. and Parsa, A. and Liu, Y. and van Duijn, C. M. and Siscovick, D. S. and Gudnason, V. and Jamshidi, Y. and Salomaa, V. and Felix, S. B. and Sanna, S. and Ritchie, M. D. and Stricker, B. H. and Stefansson, K. and Boyer, L. A. and Cappola, T. P. and Olsen, J. V. and Lage, K. and Schwartz, P. J. and Kääb, S. and Chakravarti, A. and Ackerman, M. J. and Pfeufer, A. and de Bakker, P. I. and Newton, C.. (2014) Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature genetics, Vol. 46, H. 8. pp. 826-836.

2004

Binder, E. B. and Salyakina, D. and Lichtner, P. and Wochnik, G. M. and Ising, M. and Pütz, B. and Papiol, S. and Seaman, S. and Lucae, S. and Kohli, M. A. and Nickel, T. and Künzel, H. E. and Fuchs, B. and Majer, M. and Pfennig, A. and Kern, N. and Brunner, J. and Modell, S. and Baghai, T. and Deiml, T. and Zill, P. and Bondy, B. and Rupprecht, R. and Messer, T. and Köhnlein, O. and Dabitz, H. and Brückl, T. and Müller, N. and Pfister, H. and Lieb, R. and Mueller, J. C. and Lohmussar, E. and Strom, T. and Bettecken, T. and Meitinger, T. and Uhr, M. and Rein, T. and Holsboer, F. and Müller-Myhsok, B.. (2004) Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nature genetics, Vol. 36, H. 12. pp. 1319-1325.

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