Showing 1 - 4 results of 4 for search 'de Bakker, PIW', query time: 0.03s Refine Results
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    Genetic loci associated with heart rate variability and their effects on cardiac disease risk by Nolte, IM, Munoz, ML, Tragante, V, Amare, AT, Jansen, R, Vaez, A, von der Heyde, B, Avery, CL, Bis, JC, Dierckx, B, van Dongen, J, Gogarten, SM, Goyette, P, Hernesniemi, J, Huikari, V, Hwang, SJ, Jaju, D, Kerr, KF, Kluttig, A, Krijthe, BP, Kumar, J, van der Laan, SW, Lyytikäinen, LP, Maihofer, AX, Minassian, A, van der Most, PJ, Müller-Nurasyid, M, Nivard, M, Salvi, E, Stewart, JD, Thayer, JF, Verweij, N, Wong, A, Zabaneh, D, Zafarmand, MH, Abdellaoui, A, Albarwani, S, Albert, C, Alonso, A, Ashar, F, Auvinen, J, Axelsson, T, Baker, DG, de Bakker, PIW, Barcella, M, Bayoumi, R, Bieringa, RJ, Boomsma, D, Boucher, G, Britton, AR, Christophersen, I, Dietrich, A, Ehret, GB, Ellinor, PT, Eskola, M, Felix, JF, Floras, JS, Franco, OH, Friberg, P, Gademan, MGJ, Geyer, MA, Giedraitis, V, Hartman, CA, Hemerich, D, Hofman, A, Hottenga, JJ, Huikuri, H, Hutri-Kähönen, N, Jouven, X, Junttila, J, Juonala, M, Kiviniemi, AM, Kors, JA, Kumari, M, Kuznetsova, T, Laurie, CC, Lefrandt, JD, Li, Y, Li, Y, Liao, D, Limacher, MC, Lin, HJ, Lindgren, CM, Lubitz, SA, Mahajan, A, McKnight, B, Schwabedissen, HM, Milaneschi, Y, Mononen, N, Morris, AP, Nalls, MA, Navis, G, Neijts, M, Nikus, K, North, KE, O'Connor, DT, Ormel, J, Perz, S, Peters, A, Psaty, BM, Raitakari, OT, Risbrough, VB, Sinner, MF, Siscovick, D, Smit, JH, Smith, NL, Soliman, EZ, Sotoodehnia, N, Staessen, JA, Stein, PK, Stilp, AM, Stolarz-Skrzypek, K, Strauch, K, Sundström, J, Swenne, CA, Syvänen, AC, Tardif, JC, Taylor, KD, Teumer, A, Thornton, TA, Tinker, LE, Uitterlinden, AG, van Setten, J, Voss, A, Waldenberger, M, Wilhelmsen, KC, Willemsen, G, Wong, Q, Zhang, ZM, Zonderman, AB, Cusi, D, Evans, MK, Greiser, HK, van der Harst, P, Hassan, M, Ingelsson, E, Järvelin, MR, Kääb, S, Kähönen, M, Kivimaki, M, Kooperberg, C, Kuh, D, Lehtimäki, T, Lind, L, Nievergelt, CM, O'Donnell, CJ, Oldehinkel, AJ, Penninx, B, Reiner, AP, Riese, H, van Roon, AM, Rioux, JD, Rotter, JI, Sofer, T, Stricker, BH, Tiemeier, H, Vrijkotte, TGM, Asselbergs, FW, Brundel, BJJM, Heckbert, SR, Whitsel, EA, Hoed, M, Snieder, H, de Geus, EJC

    Published 2017
    Journal article
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    Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis by Lin, K, Pulit, SL, Van Rheenen, W, Shatunov, A, Dekker, AM, McLaughlin, RL, Diekstra, FP, Van Der Spek, RAA, Võsa, U, De Jong, S, Robinson, MR, Yang, J, Fogh, I, Van Doormaal, PT, Tazelaar, GHP, Koppers, M, Blokhuis, AM, Sproviero, W, Jones, AR, Kenna, KP, Van Eijk, KR, Harschnitz, O, Schellevis, RD, Brands, WJ, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, LD, Millecamps, S, Salachas, F, Meininger, V, De Carvalho, M, Pinto, S, Mora, JS, Rojas-García, R, Polak, M, Chandran, S, Colville, S, Swingler, R, Morrison, KE, Shaw, PJ, Hardy, J, Orrell, RW, Pittman, A, Sidle, K, Fratta, P, Malaspina, A, Topp, S, Petri, S, Abdulla, S, Drepper, C, Sendtner, M, Meyer, T, Ophoff, RA, Staats, KA, Wiedau-Pazos, M, Lomen-Hoerth, C, Van Deerlin, VM, Trojanowski, JQ, Elman, L, McCluskey, L, Basak, AN, Tunca, C, Hamzeiy, H, Parman, Y, Meitinger, T, Lichtner, P, Radivojkov-Blagojevic, M, Andres, CR, Maurel, C, Bensimon, G, Landwehrmeyer, B, Brice, A, Payan, CAM, Saker-Delye, S, Dürr, A, Wood, NW, Tittmann, L, Lieb, W, Franke, A, Rietschel, M, Cichon, S, Nöthen, MM, Amouyel, P, Tzourio, C, Dartigues, J-F, Uitterlinden, AG, Rivadeneira, F, Estrada, K, Hofman, A, Curtis, C, Blauw, HM, Van Der Kooi, AJ, De Visser, M, Goris, A, Weber, M, Shaw, CE, Smith, BN, Pansarasa, O, Cereda, C, Del Bo, R, Comi, GP, D'Alfonso, S, Bertolin, C, Sorarù, G, Mazzini, L, Pensato, V, Gellera, C, Tiloca, C, Ratti, A, Calvo, A, Moglia, C, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Lunetta, C, Penco, S, Riva, N, Padovani, A, Filosto, M, Muller, B, Stuit, RJ, Registry, P, Slalom Group, Registry, S, Fals Sequencing Consortium, Slagen Consortium, Nnipps Study Group, Blair, I, Zhang, K, McCann, EP, Fifita, JA, Nicholson, GA, Rowe, DB, Pamphlett, R, Kiernan, MC, Grosskreutz, J, Witte, OW, Ringer, T, Prell, T, Stubendorff, B, Kurth, I, Hübner, CA, Leigh, PN, Casale, F, Chio, A, Beghi, E, Pupillo, E, Tortelli, R, Logroscino, G, Powell, J, Ludolph, AC, Weishaupt, JH, Robberecht, W, Van Damme, P, Franke, L, Pers, TH, Brown, RH, Glass, JD, Landers, JE, Hardiman, O, Andersen, PM, Corcia, P, Vourc'H, P, Silani, V, Wray, NR, Visscher, PM, De Bakker, PIW, Van Es, MA, Pasterkamp, RJ, Lewis, CM, Breen, G, Al-Chalabi, A, Van Den Berg, LH, Veldink, JH

    Published 2016
    Journal article