Genome-wide association study based on cardiac magnetic resonance imaging in 23,634 individuals identifies five new loci associated with left atrial enlargement von Ahlberg, G, Andreasen, L, Ghouse, J, Haunsoe, S, Svendsen, J.H, Olesen, M.S

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Rare coding variants in MYH6 are associated with atrial fibrillation: results from 45,596 exomes representing the general population von Vad, O.B, Paludan-Muller, C, Ahlberg, G, Andreasen, L, Refsgaard, L, Lundegaard, P.R, Haunso, S, Svendsen, J.H, Olesen, M.S

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Rare variants in HCN4 identified in the general population are associated with complete atrioventricular (AV) block, 1. degree AV block and bundle branch block, results from 50.000... von Jensen, J, Vad, O.B, Paludan-Muller, C, Lundegaard, P.R, Svendsen, J.H, Haunsoe, S, Bundgaard, H, Olesen, M.S

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Body composition estimated from the electrocardiogram by deep learning von Thorndal, E.M., Dons, F.E., Chevalier, M.K., Christensen, L.B., Vad, O.B., Olesen, M.S., Graff, C., Linz, D., Nørregaard, M., Isaksen, J.L., Riegler, M., Kanters, J.K.

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Left atrial late gadolinium enhancement is associated with atrial fibrillation as detected by continuous monitoring von Bertelsen, L, Diederichsen, S.Z, Haugan, K.J, Brandes, A, Graff, C, Krieger, D, Kronborg, C, Kober, L, Peters, D.C, Olesen, M.S, Hojberg, S, Vejlstrup, N, Svendsen, J.H

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Distinguishing pathogenic mutations from background genetic noise in cardiology: The use of large genome databases for genetic interpretation von Ghouse, J., Skov, M.W., Bigseth, R.S., Ahlberg, G., Kanters, J.K., Olesen, M.S.

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Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia‐associated variants von Paludan‐Müller, C., Ahlberg, G., Ghouse, J., Herfelt, C., Svendsen, J.H., Haunsø, S., Kanters, J.K., Olesen, M.S.

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Association between maternal diabetes and cardiac left ventricular structure and function in the neonate: a study from the Copenhagen Baby Heart Study von Ghouse, J, Voegg, O, Sillesen, A.S, Pihl, C, Axelsson, A.R, Vejlstrup, N, Oyen, N, Jensen, M.T, Wohlfart, J, Damm, P, Olesen, M.S, Mathiesen, E.R, Iversen, K, Bundgaard, H, Boyd, H

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Genome-wide association study of patients with atrioventricular nodal reentry tachycardia von Andreasen, L, Ahlberg, G, Hartmann, J, Paludan-Mueller, C, Jensen, H.K, Riahi, S, Hansen, J, Sandgaard, N, Haunsoe, S, Kanters, J.K, Ellervik, C, Bundgaard, H, Svendsen, J.H, Olesen, M.S

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P705Next-generation sequencing of 38 families with familial dilated cardiomyopathy von Nouhravesh, N., Ahlberg, G., Chistensen, A., Thune, J.J., Koeber, L., Hastrup Svendsen, J., Moeller, D.V., Olesen, M.S.

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Genome-wide association study of T-wave morphology von Kanters, J.K., Grarup, N., Graff, C., Nielsen, J., Linneberg, A., Hansen, T., Olesen, M.S.

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Genetical component of the QT interval is associated with increased mortality in the general population von Kanters, J.K., Ghouse, J., Skov, M.W., Isaksen, J.L., Christiansen, M., Graff, C., Grarup, N., Have, C. Theil, Linneberg, A., Hansen, T., Olesen, M.S.

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Genome-wide association study of T-wave morphology von Graff, C., Grarup, N., Hansen, T., Kanters, J.K., Linneberg, A., Nielsen, J., Olesen, M.S.

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Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications von Steinbrenner, I., Li, Y., Bujnis, M.N., Marouli, E., Galesloot, T.E., Babajide, O., Andreasen, L., Beekman, M., Bork-Jensen, J., Boutin, T., Brody, J.A., Brown, S.J., Campbell, P.J., Cappola, A.R., Ceresini, G., Concas, M.P., Cross, S.M., Cucca, F., Deary, I.J., Kjaergaard, A.D., Tcheugui, J.B.E., Ellervik, C., Ferrucci, L., Freudenberg, J., Fuchsberger, C., Giulianini, F., Gögele, M., Graham, S.E., Grarup, N., Gunjaca, I., Harding, B.N., Harris, S.E., Haunso, S., Hayward, C., Hui, J., Ittermann, T., Jukema, J.W., Kanters, J.K., Kiemeney, L.A.L.M., Kloppenburg, M., Kühnel, B., Langenberg, C., Lapauw, B., Leese, G., Liewald, D.C.M., Linneberg, A., Matana, A., Meitinger, T., Meulenbelt, I., Mitchell, B.D., Mora, S., Naitza, S., Nauck, M., Noordam, R., Nursyifa, C., Okada, Y., Onano, S., Papadopoulou, A., Palmer, C.N.A., Pedersen, O., Peters, A., Pietzner, M., Polasek, O., Pramstaller, P.P., Ray, D., Redmond, P., Richards, J.B., Ryan, K.A., Schultheiss, U.T., Selvin, E., Siddiqui, M.K., Sidore, C., Slagboom, P.E., Sorensen, T.I.A., Spector, T.D., Spedicati, B., Starr, J.M., Stott, D.J., Torlak, V., Tuhkanen, J., Uitterlinden, A.G., Akker, E.B. van den, Klauw, M.M. van der, Heemst, D. van, Verroken, C., Visser, W.E., Vojinovic, D., Waldenberger, M., Walsh, J.P., Wareham, N.J., Willer, C.J., Wilson, S.G., Wolffenbuttel, B.H.R., Wright, M.J., Zemunik, T., Zhou, W., Zhu, G., Peeters, R.P., Köttgen, A., Teumer, A.

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Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease von Young, W.J., Haessler, J., Benjamins, J.W., Repetto, L., Yao, J., Isaacs, A., Harper, A.R., Ramirez, J., Garnier, S., Duijvenboden, S. van, Baldassari, A.R., Concas, M.P., Duong, T., Foco, L., Isaksen, J.L., Mei, H., Noordam, R., Nursyifa, C., Richmond, A., Santolalla, M.L., Sitlani, C.M., Soroush, N., Thériault, S., Trompet, S., Aeschbacher, S., Ahmadizar, F., Alonso, A., Brody, J.A., Campbell, A., Correa, A., Darbar, D., Luca, A. de, Deleuze, J.F., Ellervik, C., Fuchsberger, C., Goel, A., Grace, C., Guo, X.Q., Hansen, T., Heckbert, S.R., Jackson, R.D., Kors, J.A., Lima-Costa, M.F., Linneberg, A., Macfarlane, P.W., Morrison, A.C., Navarro, P., Porteous, D.J., Pramstaller, P.P., Reiner, A.P., Risch, L., Schotten, U., Shen, X., Sinagra, G., Soliman, E.Z., Stoll, M., Tarazona-Santos, E., Tinker, A., Trajanoska, K., Villard, E., Warren, H.R., Whitsel, E.A., Wiggins, K.L., Arking, D.E., Avery, C.L., Conen, D., Girotto, G., Grarup, N., Hayward, C., Jukema, J.W., Mook-Kanamori, D.O., Olesen, M.S., Padmanabhan, S., Psaty, B.M., Pattaro, C., Ribeiro, A.L.P., Rotter, J.I., Stricker, B.H., Harst, P. van der, Duijn, C.M. van, Verweij, N., Wilson, J.G., Orini, M., Charron, P., Watkins, H., Kooperberg, C., Lin, H.J., Wilson, J.F., Kanters, J.K., Sotoodehnia, N., Mifsud, B., Lambiase, P.D., Tereshchenko, L.G., Munroe, P.B.

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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., Noordam, 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., 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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Supplementary Material for: Left Atrial Remodeling and Cerebrovascular Disease Assessed by Magnetic Resonance Imaging in Continuously Monitored Patients von L., Bertelsen, S.Z., Diederichsen, K.S., Frederiksen, K.J., Haugan, A., Brandes, C., Graff, D., Krieger, S., Højberg, M.S., Olesen, T., Biering-Sørensen, L., Køber, N., Vejlstrup, S.G., Hasselbalch, J.H., Svendsen

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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., Noordam, R., 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., 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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Impact of climate change effects on contamination of cereal grains with deoxynivalenol von Van der Fels-Klerx, H J, van Asselt, Esther D, Madsen, Marianne S, Olesen, Jørgen E

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Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors von Pfeifer, Susanne P, Hansen, Ruth M S, Olesen, Inge A, Meyts, Ewa Rajpert-De, Wilkie, Andrew O M, Goriely, Anne, McGowan, Simon J, Taylor, Indira B, McVean, Gilean A T, Jacobsen, Grete Krag

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