Sequence variants associated with BMI affect disease risk through BMI itself von Einarsson, Gudmundur, Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Zink, Florian, Helgason, Hannes, Olafsdottir, Thorhildur, Rognvaldsson, Solvi, Tragante, Vinicius, Ulfarsson, Magnus O., Sveinbjornsson, Gardar, Snaebjarnarson, Audunn S., Einarsson, Hafsteinn, Aegisdottir, Hildur M., Jonsdottir, Gudrun A., Helgadottir, Anna, Gretarsdottir, Solveig, Styrkarsdottir, Unnur, Arnason, Hannes K., Bjarnason, Ragnar, Sigurdsson, Emil, Arnar, David O., Bjornsson, Einar S., Palsson, Runolfur, Bjornsdottir, Gyda, Stefansson, Hreinn, Thorgeirsson, Thorgeir, Sulem, Patrick, Thorsteinsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel F., Stefansson, Kari

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Genetic insight into sick sinus syndrome von Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Aegisdottir, Hildur M, Benonisdottir, Stefania, Stefansdottir, Lilja, Ivarsdottir, Erna V, Halldorsson, Gisli H, Sigurdsson, Jon K, Torp-Pedersen, Christian, Weeke, Peter E, Brunak, Søren, Westergaard, David, Pedersen, Ole B, Sorensen, Erik, Nielsen, Kaspar R, Burgdorf, Kristoffer S, Banasik, Karina, Brumpton, Ben, Zhou, Wei, Oddsson, Asmundur, Tragante, Vinicius, Hjorleifsson, Kristjan E, Davidsson, Olafur B, Rajamani, Sridharan, Jonsson, Stefan, Torfason, Bjarni, Valgardsson, Atli S, Thorgeirsson, Gudmundur, Frigge, Michael L, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Helgadottir, Anna, Gretarsdottir, Solveig, Sulem, Patrick, Jonsdottir, Ingileif, Willer, Cristen J, Hveem, Kristian, Bundgaard, Henning, Ullum, Henrik, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari

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Genetic Variants Close to TTN , NKX2-5 , and MYH6 Associate With AVNRT von Andreasen, Laura, Ahlberg, Gustav, Ægisdottir, Hildur M., Sveinbjörnsson, Gardar, Lundegaard, Pia R., Hartmann, Jacob P., Paludan-Müller, Christian, Hadji-Turdeghal, Katra, Ghouse, Jonas, Pehrson, Steen, Jensen, Henrik K., Riahi, Sam, Hansen, Jim, Sandgaard, Niels, Sørensen, Erik, Banasik, Karina, Sækmose, Susanne G., Bruun, Mie T., Hjalgrim, Henrik, Erikstrup, Christian, Pedersen, Ole B., Wittig, Michael, Haunsø, Stig, Ostrowski, Sisse R., Franke, Andre, Brunak, Søren, Kanters, Jørgen K., Ellervik, Christina, Bundgaard, Henning, Ullum, Henrik, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Holm, Hilma, Arnar, David O., Stefansson, Kari, Svendsen, Jesper H., Olesen, Morten S.

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Genetic variants associated with syncope implicate neural and autonomic processes von Aegisdottir, Hildur M, Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Stefansson, Olafur A, Gunnarsson, Bjarni, Tragante, Vinicius, Thorleifsson, Gudmar, Stefansdottir, Lilja, Thorgeirsson, Thorgeir E, Ferkingstad, Egil, Sulem, Patrick, Norddahl, Gudmundur, Rutsdottir, Gudrun, Banasik, Karina, Christensen, Alex Hoerby, Mikkelsen, Christina, Pedersen, Ole Birger, Brunak, Søren, Bruun, Mie Topholm, Erikstrup, Christian, Jacobsen, Rikke Louise, Nielsen, Kaspar Rene, Sørensen, Erik, Frigge, Michael L, Hjorleifsson, Kristjan E, Ivarsdottir, Erna V, Helgadottir, Anna, Gretarsdottir, Solveig, Steinthorsdottir, Valgerdur, Oddsson, Asmundur, Eggertsson, Hannes P, Halldorsson, Gisli H, Jones, David A, Anderson, Jeffrey L, Knowlton, Kirk U, Nadauld, Lincoln D, Haraldsson, Magnus, Thorgeirsson, Gudmundur, Bundgaard, Henning, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Ostrowski, Sisse R, Holm, Hilma, Stefansson, Kari

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Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland von Sveinbjornsson, Gardar, Benediktsdottir, Bara D, Sigfusson, Gunnlaugur, Norland, Kristjan, Davidsson, Olafur B, Thorolfsdottir, Rosa B, Tragante, Vinicius, Arnadottir, Gudny A, Jensson, Brynjar O, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Gudmundsdottir, Hallbera, Aegisdottir, Hildur M, Fridriksson, Brynjar, Thorgeirsson, Gudmundur, Magnusson, Vidar, Oddsson, Asmundur, Sulem, Patrick, Gudbjartsson, Daniel F, Holm, Hilma, Arnar, David O, Stefansson, Kari

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Genetic insight into sick sinus syndrome von Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Aegisdottir, Hildur M, Benonisdottir, Stefania, Stefansdottir, Lilja, Ivarsdottir, Erna V, Halldorsson, Gisli H, Sigurdsson, Jon K, Torp-Pedersen, Christian, Weeke, Peter E, Brunak, Søren, Westergaard, David, Pedersen, Ole B, Sorensen, Erik, Nielsen, Kaspar R, Burgdorf, Kristoffer S, Banasik, Karina, Brumpton, Ben, Zhou, Wei, Oddsson, Asmundur, Tragante, Vinicius, Hjorleifsson, Kristjan E, Davidsson, Olafur B, Rajamani, Sridharan, Jonsson, Stefan, Torfason, Bjarni, Valgardsson, Atli S, Thorgeirsson, Gudmundur, Frigge, Michael L, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Helgadottir, Anna, Gretarsdottir, Solveig, Sulem, Patrick, Jonsdottir, Ingileif, Willer, Cristen J, Hveem, Kristian, Bundgaard, Henning, Ullum, Henrik, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari

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Incidence of osmotic demyelination syndrome in Sweden: A nationwide study von Aegisdottir, Hildur, Cooray, Charith, Wirdefeldt, Karin, Piehl, Fredrik, Sveinsson, Olafur

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Abstract 13222: Genetic Variants Close to NKX2-5 and MYH6 Are Associated With AV Nodal Reentry Tachycardia in First Genome-Wide Association Study von Andreasen, Laura, Ahlberg, Gustav, Lundegaard, Pia Rengtved, Ægisdottir, Hildur, Hartmann, Jacob Peter, Paludan-Mueller, Christian, Hadji-Turdeghal, Katra, Ghouse, Jonas, Pehrson, Steen, Jensen, Henrik, Riahi, Sam, Hansen, Jim, Sandgaard, Niels, Haunso, stig, Kanters, Jorgen, Ellervik, Christina, Bundgaard, Henning, Ullum, Henrik, Holm, Hilma, Arnar, David, Svendsen, Jesper Hastrup, Olesen, Morten

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Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT von Andreasen, Laura, Ahlberg, Gustav, Ægisdóttir, Hildur M., Sveinbjörnsson, Gardar, Lundegaard, Pia R., Hartmann, Jacob P., Paludan-Müller, Christian, Hadji-Turdeghal, Katra, Ghouse, Jonas, Pehrson, Steen, Jensen, Henrik K., Riahi, Sam, Hansen, Jim, Sandgaard, Niels, Sørensen, Erik, Banasik, Karina, Sækmose, Susanne G., Bruun, Mie T., Hjalgrim, Henrik, Erikstrup, Christian, Pedersen, Ole B., Wittig, Michael, Haunsø, Stig, Ostrowski, Sisse R., Genomic Consortium, DBDS, Franke, Andre, Brunak, Søren, Kanters, Jørgen K., Ellervik, Christina, Bundgaard, Henning, Ullum, Henrik, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Holm, Hilma, Arnar, David O., Stefansson, Kari, Svendsen, Jesper H., Olesen, Morten S.

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Genetic insight into sick sinus syndrome von Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Aegisdottir, Hildur M, Benonisdottir, Stefania, Stefánsdóttir, Lilja, Ivarsdottir, Erna V, Halldorsson, Gisli H, Sigurdsson, Jon K, Torp-Pedersen, Christian, Weeke, Peter E, Brunak, Søren, Westergaard, David, Pedersen, Ole B, Sorensen, Erik, Nielsen, Kaspar R, Burgdorf, Kristoffer S, Banasik, Karina, Brumpton, Ben Michael, Zhou, Wei, Oddsson, Asmundur, Tragante, Vinicius, Hjorleifsson, Kristjan E, Davidsson, Olafur B, Rajamani, Sridharan, Jonsson, Stefan, Torfason, Bjarni, Valgardsson, Atli S, Thorgeirsson, Gudmundur, Frigge, Michael L, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Helgadottir, Anna, Gretarsdotti, Solveig, Sulem, Patrick, Jonsdottir, Ingileif, Willer, Cristen J, Hveem, Kristian, Bundgaard, Henning, Ullum, Henrik, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari

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