Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: A genome-wide association study of 13,372 participants von Deo, R., MD, MTR, Nalls, M.A., PhD, Avery, C.L., PhD, Smith, J.G., MD, Evans, D.S., PhD, MPH, Keller, M.F., BS, Butler, A.M., MS, Buxbaum, S.G., PhD, Li, G., MS, Miguel Quibrera, P., MS, Smith, E.N., PhD, Tanaka, T., PhD, Akylbekova, E.L., MS, Alonso, A., MD, PhD, Arking, D.E., PhD, Benjamin, E.J., MD, ScM, Berenson, G.S., MD, Bis, J.C., PhD, Chen, L.Y., MD, FHRS, Chen, W., MD, PhD, Cummings, S.R., MD, Ellinor, P.T., MD, PhD, Evans, M.K., MD, Ferrucci, L., MD, PhD, Fox, E.R., MD, MPH, Heckbert, S.R., MD, PhD, Heiss, G., MD, PhD, Hsueh, W.C., MPH, PhD, Kerr, K.F., PhD, Limacher, M.C., MD, Liu, Y., MD, PhD, Lubitz, S.A., MD, MPH, Magnani, J.W., MD, Mehra, R., MD, MS, Marcus, G.M., MD, MAS, FHRS, Murray, S.S., PhD, Newman, A.B., MD, MPH, Njajou, O., PhD, ScD, North, K.E., PhD, Paltoo, D.N., MD, MPH, Psaty, B.M., MD, PhD, Redline, S.S., MD, MPH, Reiner, A.P., MD, MSc, Robinson, J.G., MD, MPH, Rotter, J.I., MD, Samdarshi, T.E., MD, MPH, Schnabel, R.B., MD, MSc, Schork, N.J., PhD, Singleton, A.B., PhD, Siscovick, D., MD, MPH, Soliman, E.Z., MD, MSc, MS, Sotoodehnia, N., MD, MPH, Srinivasan, S.R., PhD, Taylor, H.A., MD, MPH, Trevisan, M., MD, Zhang, Z., MD, MPH, Zonderman, A.B., PhD, Newton-Cheh, C., MD, MPH, Whitsel, E.A., MD, MPH

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Distinctive pharmacology and kinetics of cloned neuronal Ca2+ channels and their possible counterparts in mammalian CNS neurons von ZHANG, J.-F, RANDALL, A. D, ELLINOR, P. T, HORNE, W. A, SATHER, W. A, TANABE, T, SCHWARZ, T. L, TSIEN, R. W

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Genetic burden of TNNI3K in diagnostic testing of patients with dilated cardiomyopathy and supraventricular arrhythmias von Pham, C., Andrzejczyk, K., Jurgens, S.J., Deprez, R.L., Palm, K.C.A., Vermeer, A.M.C., Nijman, J., Christiaans, I., Barge-Schaapveld, D.Q.C.M., Dessel, P.F.H.M. van, Beekman, L., Choi, S.H., Lubitz, S.A., Skoric-Milosavljevic, D., Bersselaar, L. van den, Jansen, P.R., Copier, J.S., Ellinor, P.T., Wilde, A.A.M., Bezzina, C.R., Lodder, E.M.

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Overlap of genetic loci for central serous chorioretinopathy with age-related macular degeneration (vol. 141, pg. 499, 2023) von Rämö, J.T., Abner, E., Dijk, E.H.C. van, Wang, X., Brinks, J., Nikopensius, T., Noukas, M., Marjonen, H., Silander, K., Jukarainen, S., Kiiskinen, T., Choi, S.H., Kajanne, R., Mehtonen, J., Palta, P., Lubitz, S.A., Kaarniranta, K., Sobrin, L., Kurki, M., Yzer, S., Ellinor, P.T., Esko, T., Daly, M.J., Hollander, A.I. den, Palotie, A., Turunen, J.A., Boon, C.J.F., Rossin, E.J.

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Overlap of genetic loci for central serous chorioretinopathy with age-related macular degeneration von Ramo, J., Abner, E., Dijk, E.H.C. van, Wang, X., Brinks, J., Nikopensius, T., Noukas, M., Marjonen, H., Silander, K., Jukarainen, S., Kiiskinen, T., Choi, S.H., Kajanne, R., Mehtonen, J., Palta, P., Lubitz, S.A., Kaarniranta, K., Sobrin, L., Kurki, M., Yzer, S., Ellinor, P.T., Esko, T., Daly, M.J., Hollander, A.I. den, Palotie, A., Turunen, J.A., Boon, C.J.F., Rossin, E.J.

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Identification of functional variant enhancers associated with atrial fibrillation von Ouwerkerk, A.F. van, Bosada, F.M., Liu, J., Zhang, J., Duijvenboden, K. van, Chaffin, M., Tucker, N.R., Pijnappels, D., Ellinor, P.T., Barnett, P., Vries, A.A.F. de, Christoffels, V.M.

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Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways von Lahrouchi, N., Isaacs, A., Duong, T.V., Ahmed, F., Brody, J.A., Salman, R., Benjamins, J.W., Lyytikainen, L.P., Berg, M.E. van den, Weiss, S., Cook, J.P., Evans, D.S., Freudling, R., Isaksen, J.L., Lin, H.H., Mei, H., Moscati, A., Muller-Nurasyid, M., Nursyifa, C., Qian, Y., Roselli, C., Warren, H.R., Raza, D., Aeschbacher, S., Alonso, A., Bis, J.C., Campbell, A., Cocca, M., Cutler, M.J., Darbar, D., Grandi, A. de, Luca, A. de, Ding, J., Ellervik, C., Ellinor, P.T., Felix, S.B., Froguel, P., Fuchsberger, C., Gogele, M., Graff, M., Guo, X.Q., Heckbert, S.R., Huang, P.L., Hutri-Kahonen, N., Kavousi, M., Kors, J.A., Lin, H.J., Lind, L., Linneberg, A., Liu, S.M., Meitinger, T., Mezzavilla, M., Mononen, N., Montasser, M.E., Nauck, M., Nauffal, V., Nikus, K., Patton, K.K., Pramstaller, P.P., Reiner, A.P., Ribeiro, A.L.P., Rice, K.M., Risch, L., Schurmann, C., Sinagra, G., Soliman, E.Z., Tarasov, K., Tinker, A., Trompet, S., Volker, U., Waldenberger, M., Weng, L.C., Wilson, J.G., Conen, D., Gharib, S.A., Girotto, G., Grarup, N., Hayward, C., Jamshidi, Y., Jukema, J.W., Kahonen, M., Lehtimaki, T., Lima-Costa, M.F., Liu, Y.M., Loos, R.J.F., Lubitz, S.A., Mook-Kanamori, D.O., O'Connell, J.R., Olesen, M.S., Orini, M., Padmanabhan, S., Peters, A., Psaty, B.M., Rotter, J.I., Stricker, B., Verweij, N., Arking, D.E., Lambiase, P.D., Sotoodehnia, N., Newton-Cheh, C.

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The genomics of heart failure: design and rationale of the HERMES consortium von Shah, S., Lin, H.H., Henry, A., Swerdlow, D.I., Andersson, C., Verweij, N., Holmes, M.V., Arnlov, J., Svensson, P., Sallah, N., Almgren, P., Aragam, K.G., Backman, J.D., Bloom, H.L., Boersma, E., Brandimarto, J., Brown, M.R., Brunner-La Rocca, H.P., Chasman, D.I., Chazara, O., Chen, X., Cleland, J.G.F., Cook, J.P., Denus, S. de, Dehghan, A., Delgado, G.E., Denaxas, S., Dorr, M., Dudley, S.C., Engstrom, G., Esko, T., Fatemifar, G., Felix, S.B., Finan, C., Ford, I., Fougerousse, F., Fouodjio, R., Ghanbari, M., Ghasemi, S., Giulianini, F., Gross, S., Gudbjartsson, D.F., Gutmann, R., Haggerty, C.M., Harst, P. van der, Hillege, H., Hyde, C.L., Jacob, J., Jukema, J.W., Kamanu, F., Kavousi, M., Kober, L., Kuchenbaecker, K., Langenberg, C., Lind, L., London, B., Mahajan, A., Marston, N.A., Marz, W., Melloni, G., Morley, M.P., Morris, A.D., Morris, A.P., Nagle, M.W., Nelson, C.P., Newton-Cheh, C., Niiranen, T., Owens, A.T., Pare, G., Perola, M., Perreault, L.P.L., Portilla-Fernandez, E., Rice, K.M., Ruff, C.T., Setten, J. van, Shalaby, A.A., Smelser, D.T., Thorgeirsson, G., Trompet, S., Uitterlinden, A.G., Vaura, F., Veluchamy, A., Visscher, P.M., Weiss, R., White, H.D., Wiggins, K.L., Yang, J., Yang, Y.F., Yerges-Armstrong, L.M., Yu, B., Zhao, F.Y., Holm, H., Sattar, N., Lanfear, D.E., Asselbergs, F.W., Hingorani, A.D., Dube, M.P., Samani, N.J., Lang, C.C., Smith, J.G.

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, C, Postema, P.G, Amin, Ahmad S, Nannenberg, E.A, Ware, J.S, Whiffin, N, Mazzarotto, F, Korić-Milosavljević, D, Krijger, C, Arbelo, Elena, Babuty, D, Barajas-Martinez, H, Beckmann, B.M, Bézieau, S, Bos, J.M, Breckpot, J, Campuzano Larrea, Oscar, Castelletti, S, Celen, C, Clauss, S, Corveleyn, A, Crotti, Lia, Dagradi, F, de Asmundis, C, Denjoy, Isabelle, Dittmann, S, Ellinor, P.T, Ortuño, C.G, Giustetto, Carla, Gourraud, Jean Baptiste, Hazeki, D, Horie, M, Ishikawa, T, Itoh, H

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Genetic deeterminants of electrocardiographic P-wave duration and relation to atrial fibrillation von Weng, L.C., Hall, A.W., Choi, S.H., Jurgens, S.J., Haessler, J., Bihlmeyer, N.A., Grarup, N., Lin, H.H., Teumer, A., Li-Gao, R.F., Yao, J., Guo, X.Q., Brody, J.A., Muller-Nurasyid, M., Schramm, K., Verweij, N., Berg, M.E. van den, Setten, J. van, Isaacs, A., Ramirez, J., Warren, H.R., Padmanabhan, S., Kors, J.A., Boer, R.A. de, Meer, P. van der, Sinner, M.F., Waldenberger, M., Psaty, B.M., Taylor, K.D., Volker, U., Kanters, J.K., Li, M., Alonso, A., Perez, M.V., Vaartjes, I., Bots, M.L., Huang, P.L., Heckbert, S.R., Lin, H.J., Kornej, J., Munroe, P.B., Duijn, C.M. van, Asselbergs, F.W., Stricker, B.H., Harst, P. van der, Kaab, S., Peters, A., Sotoodehnia, N., Rotter, J.I., Mook-Kanamori, D.O., Dorr, M., Felix, S.B., Linneberg, A., Hansen, T., Arking, D.E., Kooperberg, C., Benjamin, E.J., Lunetta, K.L., Ellinor, P.T., Lubitz, S.A.

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction von Ntalla, I., Cartwright, J.H., Tucker, N.R., Choi, S.H., Chaffin, M.D., Roselli, C., Barnes, M.R., Hayward, C., Marten, J., Gasparini, P., Araujo, N.M., Ribeiro, A.L.P., Souza, R.P., Tarazona-Santos, E., Giedraitis, V., Mahajan, A., Morris, A.P., Foco, L., Gogele, M., Lind, L., Lindgren, C.M., Sundstrom, J., Nelson, C.P., Kahonen, M., Mononen, N., Nikus, K., Caulfield, M.J., Padmanabhan, S., Montasser, M.E., Aeschbacher, S., Conen, D., Theriault, S., Lehtimaki, T., Barnes, C.L.K., Campbell, H., Joshi, P.K., Wilson, J.F., Kors, J.A., Duijn, C.M. van, Huang, P.L., Harris, T.B., Smith, A.V., Bottinger, E.P., Loos, R.J.F., Nadkarni, G.N., Preuss, M.H., Wilson, J., Meitinger, T., Muller-Nurasyid, M., Spector, T.D., Rienstra, M., Vegte, Y.J. van de, Verweij, N., Schramm, K., Olesen, M., Shoemaker, M.B., Brody, J.A., Psaty, B.M., Rice, K., Grandi, A. de, Fuchsberger, C., Pattaro, C., Ford, I., Jukema, J.W., Macfarlane, P.W., Trompet, S., Volker, U., Jula, A., Saaksjarvi, K., Salomaa, V., Guo, X.Q., Rotter, J.I., Taylor, K.D., Yao, J., Mutsert, R. de, Mook-Kanamori, D.O., Lakatta, E.G., Qian, Y., Lunetta, K.L., Smith, B.H., Berg, M.E. van den, Haessler, J., Kooperberg, C., Peters, U., Reiner, A.P., Alonso, A., Arking, D.E., Gogarten, S.M., Kerr, K.F., Laurie, C.C., Seyerle, A.A., Duijvenboden, S. van, Arnar, D.O., Gudbjartsson, D.F., Holm, H., Thorleifsson, G., Tinker, A., Ellinor, P.T., Jamshidi, Y., Lubitz, S.A.

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure von Lin, H.H., Hedman, A.K., Morley, M.P., Helgadottir, A., Dehghan, A., Almgren, P., Andersson, C., Brandimarto, J., Brown, M.R., Buckbinder, L., Chasman, D.I., Chung, J., Denaxas, S., Dunn, M.E., Engstrom, G., Felix, S.B., Finan, C., Ford, I., Ghasemi, S., Gottdiener, J.S., Gudbjartsson, D.F., Gutmann, R., Harst, P. van der, Ingelsson, E., Jukema, J.W., Lind, L., Lindgren, C.M., London, B., Lotta, L.A., Magnusson, P., Mahajan, A., Marz, W., Mordi, I.R., Morris, A.D., Morris, A.P., Morrison, A.C., Nagle, M.W., Niiranen, T., Owens, A.T., Perola, M., Portilla-Fernandez, E., Rice, K.M., Ridker, P.M., Rotter, J.I., Salomaa, V., Shalaby, A.A., Smith, N.L., Stender, S., Stott, D.J., Tammesoo, M.L., Thorgeirsson, G., Thorsteinsdottir, U., Uitterlinden, A.G., Volker, U., Voors, A.A., Wang, X.S., Waterworth, D., Weeke, P.E., Weiss, R., Wiggins, K.L., Yerges-Armstrong, L.M., Yu, B., Zhao, J.H., Hemingway, H., Samani, N.J., Newton-Cheh, C., Malarstig, A., Lubitz, S.A., Sattar, N., Cappola, T.P., Kuchenbaecker, K., Ellinor, P.T., Smith, J.G., Swerdlow, D.I., Lumbers, R.T., Abecasis, G., Bai, X.D., Balasubramanian, S., Banerjee, N., Barnard, L., Damask, A., Dewey, F., Fuller, E.D., Gurski, L., Hahn, Y., Hawes, A., Khalid, S., Li, A., Lin, N., Lopez, A., Manoochehri, K., Mitnaul, L.J., Overton, J.D., Paulding, C., Reid, J.G., Shuldiner, A., Ulloa, R.H., Widom, L., Yadav, A., Ye, B.

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Multi-ethnic genome-wide association study for atrial fibrillation von Chaffin, M.D., Weng, L.C., Ahlberg, G., Almgren, P., Alonso, A., Benjamin, E.J., Bis, J.C., Bloom, H.L., Boerwinkle, E., Bottinger, E.B., Calkins, H., Campbell, A., Cappola, T.P., Carlquist, J., Chasman, D.I., Chen, L.Y., Chen, Y.D.I., Choi, E.K., Choi, S.H., Christophersen, I.E., Crijns, H.J., Daniels, B.R., Denny, J.C., Dichgans, M., Esa, N., Felix, S.B., Ford, I., Franco, O.H., Grewal, R.P., Gudnason, V., Gustafsson, S., Hamsten, A., Heckbert, S.R., Hernesniemi, J., Huang, J., Ipek, E.G., Jimenez-Conde, J., Johnson, R., Kahonen, M., Kamatani, Y., Kastrati, A., Katschnig-Winter, P., Kavousi, M., Kessler, T., Kirchhof, P., Kleber, M.E., Knight, S., Kubo, M., Lemaitre, R.N., Li, M., Lin, H.H., Lind, L., Lindgren, C.M., Lokki, M.L., Lyytikainen, L.P., Mahajan, A., Marcus, G.M., Margolin, L., Marz, W., Melander, O., Mohanty, S., Montgomery, J.A., Muller-Nurasyid, M., Niemeijer, M.N., Nilsson, P., Oellers, H., Padmanabhan, S., Pare, G., Pedersen, N.L., Pera, J., Refsgaard, L., Risch, L., Rost, N., Sandhu, R.K., Schnabel, R.B., Seppala, I., Shalaby, A.A., Shim, J., Shoemaker, M.B., Siland, J.E., Smith, B.H., Smith, J.G., Smith, J.D., Sun, H., Svendsen, J.H., Tanaka, T., Trompet, S., Tveit, A., Harst, P. van der, Gelder, I.C. van, Verweij, N., Vlachopoulou, E., Wang, B.Q., Weiss, R., Wiggins, K.L., Woo, D., Yoneda, Z.T., Zeng, L.Y., Lubitz, S.A., Lunetta, K.L.

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PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity von Brody, J.A., Butler, A.M., Campbell, H., Greco, F.M. del, Evans, D.S., Gibson, Q., Gudbjartsson, D.F., Lyytikainen, L.P., Muller, C., Muller-Nurasyid, M., Nolte, I.M., Padmanabhan, S., Ritchie, M.D., Smith, A.V., Steri, M., Teumer, A., Trompet, S., Ulivi, S., Yin, X.Y., Asselbergs, F.W., Bader, J.S., Barnard, J., Bis, J., Blankenberg, S., Boerwinkle, E., Bradford, Y., Buckley, B.M., Chung, M.K., Hoed, M. den, Denny, J.C., Dominiczak, A.F., Ehret, G.B., Eijgelsheim, M., Ellinor, P.T., Franco, O.H., Franke, L., Harris, T.B., Ilaria, G., Iorio, A., Kolcic, I., Kors, J.A., Lakatta, E.G., Launer, L.J., Lin, H.H., Lin, H.J., Loos, R.J.F., Lubitz, S.A., Macfarlane, P.W., Magnani, J.W., Leach, I.M., Meitinger, T., Mitchell, B.D., Munzel, T., Papanicolaou, G.J., Peters, A., Pfeufer, A., Raitakari, O.T., Rotter, J.I., Rudan, I., Samani, N.J., Schlessinger, D., Sinner, M.F., Snieder, H., Soliman, E.Z., Spector, T.D., Stott, D.J., Strauch, K., Tarasov, K.V., Uitterlinden, A.G., Wagoner, D.R. van, Volker, U., Volzke, H., Waldenberger, M., Alonso, A., Avery, C.L., Bandinelli, S., Benjamin, E.J., Cucca, F., Dorr, M., Ferrucci, L., Gasparini, P., Gudnason, V., Hayward, C., Heckbert, S.R., Hicks, A.A., Liu, Y.M., Polasek, O., Psaty, B.M., Roden, D.M., Schnabel, R.B., Sinagra, G., Stefansson, K., Stricker, B.H., Harst, P. van der, Wilson, J.F., Gharib, S.A., Bakker, P.I.W. de, Isaacs, A., Arking, D.E., Sotoodehnia, N.

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Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 von Mead, T.J., Brody, J.A., Sveinbjornsson, G., Bihlmeyer, N.A., Berg, M. van den, Bork-Jensen, J., Duijvenboden, S. van, Klena, N.T., Liu, X.Q., Gulec, C., Grarup, N., Haessler, J., Hall, L.M., Isaacs, A., Li-Gao, R.F., Lin, H.H., Liu, C.T., Lyytikainen, L.P., Marten, J., Mei, H., Muller-Nurasyid, M., Orini, M., Padmanabhan, S., Radmanesh, F., Ramirez, J., Robino, A., Schwartz, M., Smith, A.V., Verweij, N., Warren, H.R., Weiss, S., Alonso, A., Arnar, D.O., Bots, M.L., Boer, R.A. de, Dominiczak, A.F., Eijgelsheim, M., Ellinor, P.T., Guo, X.Q., Felix, S.B., Harris, T.B., Hayward, C., Heckbert, S.R., Huang, P.L., Jukema, J.W., Kahonen, M., Lambiase, P.D., Launer, L.J., Linneberg, A., Nelson, C.P., Pedersen, O., Perez, M., Peters, A., Polasek, O., Raitakari, O.T., Rice, K.M., Rotter, J.I., Sinner, M.F., Soliman, E.Z., Spector, T.D., Strauch, K., Tinker, A., Trompet, S., Uitterlinden, A., Vaartjes, I., Meer, P. van der, Volker, U., Volzke, H., Waldenberger, M., Wilson, J.G., Xie, Z.J., Asselbergs, F.W., Dorr, M., Duijn, C.M. van, Gasparini, P., Gudbjartsson, D.F., Gudnason, V., Hansen, T., Kaab, S., Kanters, J.K., Kooperberg, C., Lehtimaki, T., Lin, H.J., Lubitz, S.A., Mook-Kanamori, D.O., Conti, F.J., Newton-Cheh, C.H., Rosand, J., Sinagra, G., Smith, B.H., Holm, H., Stricker, B.H., Ulivi, S., Sotoodehnia, N., Apte, S.S., Harst, P. van der, Stefansson, K., Arking, D.E., , C.W. lo, Jamshidi, Y.

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Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval von Lin, H.H., Setten, J. van, Smith, A.V., Bihlmeyer, N.A., Warren, H.R., Brody, J.A., Radmanesh, F., Hall, L., Grarup, N., Muller-Nurasyid, M., Boutin, T., Verweij, N., Lin, H.J., Li-Gao, R.F., Berg, M.E. van den, Marten, J., Weiss, S., Prins, B.P., Haessler, J., Lyytikainen, L.P., Mei, H., Harris, T.B., Launer, L.J., Li, M., Alonso, A., Soliman, E.Z., Connell, J.M., Huang, P.L., Weng, L.C., Jameson, H.S., Hucker, W., Hanley, A., Tucker, N.R., Chen, Y.D.I., Bis, J.C., Rice, K.M., Sitlani, C.M., Kors, J.A., Xie, Z.J., Wen, C.P., Magnani, J.W., Nelson, C.P., Kanters, J.K., Sinner, M.F., Strauch, K., Peters, A., Waldenberger, M., Meitinger, T., Bork-Jensen, J., Pedersen, O., Linneberg, A., Rudan, I., Boer, R.A. de, Meer, P. van der, Yao, J., Guo, X.Q., Taylor, K.D., Sotoodehnia, N., Rotter, J.I., Mook-Kanamori, D.O., Trompet, S., Rivadeneira, F., Uitterlinden, A., Eijgelsheim, M., Padmanabhan, S., Smith, B.H., Volzke, H., Mangino, M., Spector, T.D., Bots, M.L., Perez, M., Kahonen, M., Raitakari, O.T., Gudnason, V., Arking, D.E., Munroe, P.B., Psaty, B.M., Duijn, C.M. van, Benjamin, E.J., Rosand, J., Samani, N.J., Hansen, T., Kaab, S., Polasek, O., Harst, P. van der, Heckbert, S.R., Jukema, J.W., Stricker, B.H., Hayward, C., Dorr, M., Jamshidi, Y., Asselbergs, F.W., Kooperberg, C., Lehtimaki, T., Wilson, J.G., Ellinor, P.T., Lubitz, S.A., Isaacs, A.

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes von Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Rutten-Jacobs, L., Laan, S.W. van der, Anderson, C.D., Chong, M., Adams, H.H.H., Ago, T., Amouyel, P., Ay, H., Boncoraglio, G.B., Brown, R.D., Carrera, C., Carty, C.L., Chasman, D.I., Chen, W.M., Cole, J.W., Danesh, J., Duan, Q., Engelter, S.T., Gudnason, V., Gustafsson, S., Haessler, J., Havulinna, A.S., Howard, G., Hyacinth, H.I., Ikram, M.A., Jian, X.Q., Johnson, J.A., Jukema, J.W., Kanai, M., Keene, K.L., Kissela, B.M., Kleindorfer, D.O., Kooperberg, C., Kubo, M., Lange, L.A., Launer, L.J., Leys, D., Lindgren, A.G., Lorentzen, E., Maguire, J., Meschia, J.F., Mosley, T.H., Nalls, M.A., Ninomiya, T., O'Donnell, M.J., Pulit, S.L., Rannikmae, K., Rexrode, K.M., Ridker, P.M., Rost, N.S., Rundek, T., Sacco, R.L., Sakaue, S., Sale, M.M., Schmidt, R., Schminke, U., Slowik, A., Sudlow, C.L.M., Tanislav, C., Thorsteinsdottir, U., Tzourio, C., Duijn, C.M. van, Walters, M., Wareham, N.J., Wiggins, K.L., Yang, Q., Yusuf, S., Ruusalepp, A., Schadt, E.E., Koplev, S., Smith, N.L., Lubitz, S.A., Ellinor, P.T., Tai, E.S., He, J., Harst, P. van der, Elliott, P., Chambers, J.C., Takeuchi, F., Sanghera, D.K., Jern, C., Strbian, D., Longstreth, W.T., Hata, J., Woo, D., Rosand, J., Pare, G., Hopewell, J.C., Saleheen, D., Stefansson, K., Kittner, S.J., Fornage, M., Markus, H.S., Howson, J.M.M., Kamatani, Y., Dichgans, M.

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Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium von Weng, L.C., Lunetta, K.L., Muller-Nurasyid, M., Smith, A.V., Theriault, S., Weeke, P.E., Barnard, J., Bis, J.C., Lyytikainen, L.P., Kleber, M.E., Martinsson, A., Lin, H.J., Rienstra, M., Trompet, S., Krijthe, B.P., Dorr, M., Klarin, D., Chasman, D.I., Sinner, M.F., Waldenberger, M., Launer, L.J., Harris, T.B., Soliman, E.Z., Alonso, A., Pare, G., Teixeira, P.L., Denny, J.C., Shoemaker, M.B., Wagoner, D.R. van, Smith, J.D., Psaty, B.M., Sotoodehnia, N., Taylor, K.D., Kahonen, M., Nikus, K., Delgado, G.E., Melander, O., Engstrom, G., Yao, J., Guo, X.Q., Christophersen, I.E., Ellinor, P.T., Geelhoed, B., Verweij, N., Macfarlane, P., Ford, I., Heeringa, J., Franco, O.H., Uitterlinden, A.G., Volker, U., Teumer, A., Rose, L.M., Kaab, S., Gudnason, V., Arking, D.E., Conen, D., Roden, D.M., Chung, M.K., Heckbert, S.R., Benjamin, E.J., Lehtimaki, T., Marz, W., Smith, J.G., Rotter, J.I., Harst, P. van der, Jukema, J.W., Stricker, B.H., Felix, S.B., Albert, C.M., Lubitz, S.A.

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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity von Schurmann, C., Esko, T., Graff, M., Guo, X.Q., Locke, A.E., Sivapalaratnam, S., Alfred, T., Abecasis, G., Alam, D.S., Alharthi, S.E., Asselbergs, F.W., Auer, P.L., Benn, M., Bergmann, S., Bielak, L.F., Boehnke, M., Bottinger, E.P., Brumat, M., Campbell, P.T., Cappellani, S., Carey, D.J., Chowdhury, R., Christensen, C., Cook, J.P., Cox, A.J., D'Eustacchio, A., Danesh, J., Groot, M.C.H., Mutsert, R., Dedoussis, G., Hollander, A.I., Denny, J.C., Easton, D.F., Ellinghaus, D., Farmaki, A.E., Faul, J.D., Fauser, S., Ford, I., Franco, O.H., Franke, A., Franks, P.W., Galesloot, T.E., Gandin, I., Giedraitis, V., Gordon-Larsen, P., Griffiths, H.L., Gudnason, V., Hammerschlag, A.R., Have, C.T., Hayward, C., Heid, I.M., Hernesniemi, J., Howson, J.M.M., Jansson, J.H., Jarvik, G.P., Jia, Y., Jorgensen, T., Jukema, J.W., Kahn, R.S., Kamstrup, P.R., Karaleftheri, M., Karpe, F., Kee, F., Kooner, J.S., Kuulasmaa, K., Kuusisto, J., Laakso, M., Lange, E.M., Lange, L.A., Larson, E.B., Lehtimaki, T., Lewis, C.E., Lin, K.H., Lind, L., Liu, C.T., Liu, Y.M., Loukola, A., Luan, J., Lyytikainen, L.P., Mannisto, S., Marenne, G., McKean-Cowdin, R., Moilanen, L., Montgomery, G.W., Morris, A.P., Nyholt, D.R., Owen, K.R., Padmanabhan, S., Palmer, C.N.A., Palmer, N.D., Patel, A.P., Pedersen, O., Pennell, C.E., Pers, T.H., Petersen, E.R.B., Peyser, P.A., Pirie, A., Polasek, O., Polderman, T.J., Puolijoki, H.

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ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals von Bihlmeyer, N.A., Brody, J.A., Smith, A.V., Warren, H.R., Lin, H.H., Isaacs, A., Liu, C.T., Marten, J., Radmanesh, F., Hall, L.M., Grarup, N., Mei, H., Muller-Nurasyid, M., Huffman, J.E., Verweij, N., Guo, X.Q., Yao, J., Li-Gao, R.F., Berg, M. van den, Weiss, S., Prins, B.P., Setten, J. van, Haessler, J., Lyytikainen, L.P., Li, M., Alonso, A., Soliman, E.Z., Bis, J.C., Austin, T., Chen, Y.D.I., Psaty, B.M., Harrris, T.B., Launer, L.J., Padmanabhan, S., Dominiczak, A., Huang, P.L., Xie, Z.J., Ellinor, P.T., Kors, J.A., Campbell, A., Murray, A.D., Nelson, C.P., Tobin, M.D., Bork-Jensen, J., Hansen, T., Pedersen, O., Linneberg, A., Sinner, M.F., Peters, A., Waldenberger, M., Meitinger, T., Perz, S., Kolcic, I., Rudan, I., Boer, R.A. de, Meer, P. van der, Lin, H.J., Taylor, K.D., Mutsert, R. de, Trompet, S., Jukema, J.W., Maan, A.C., Stricker, B.H.C., Rivadeneira, F., Uitterlinden, A., Volker, U., Homuth, G., Volzke, H., Felix, S.B., Mangino, M., Spector, T.D., Bots, M.L., Perez, M., Raitakari, O.T., Kahonen, M., Mononen, N., Gudnason, V., Munroe, P.B., Lubitz, S.A., Duijn, C.M. van, Newton-Cheh, C.H., Hayward, C., Rosand, J., Samani, N.J., Kanters, J.K., Wilson, J.G., Kaab, S., Polasek, O., Harst, P. van der, Heckbert, S.R., Rotter, J.I., Mook-Kanamori, D.O., Eij-Gelsheim, M., Dorr, M., Jamshidi, Y., Asselbergs, F.W., Kooperberg, C., Lehtimaki, T., Arking, D.E., Sotoodehnia, N.

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