Atrial fibrillation: the role of common and rare genetic variants

Por Olesen, Morten S, Nielsen, Morten W, Haunsø, Stig, Svendsen, Jesper H
Publicado em 2014

Making post-mortem implantable cardioverter defibrillator explantation safe

Por Räder, Sune B.E.W., Zeijlemaker, Volkert, Pehrson, Steen, Svendsen, Jesper H.
Publicado em 2009

A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation

Por Henningsen, Kristoffer M A, Olesen, Morten S, Sajadieh, Golnaz, Haunsoe, Stig, Svendsen, Jesper H
Publicado em 2013

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis

Por Winkel, Bo G, Hollegaard, Mads V, Olesen, Morten S, Svendsen, Jesper H, Haunsø, Stig, Hougaard, David M, Tfelt-Hansen, Jacob
Publicado em 2011

Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy

Por Nouhravesh, Nina, Ahlberg, Gustav, Ghouse, Jonas, Andreasen, Charlotte, Svendsen, Jesper H., Haunsø, Stig, Bundgaard, Henning, Weeke, Peter E., Olesen, Morten S.
Publicado no Mol Genet Genomic Med (2016)

The effect of constructing versus solving virtual patient cases on transfer of learning: a randomized trial

Por Tolsgaard, Martin G., Jepsen, Rikke M. H. G., Rasmussen, Maria B., Kayser, Lars, Fors, Uno, Laursen, Lars C., Svendsen, Jesper H., Ringsted, Charlotte
Publicado no Perspect Med Educ (2016)

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

Por Andreasen, Charlotte, Nielsen, Jonas B, Refsgaard, Lena, Holst, Anders G, Christensen, Alex H, Andreasen, Laura, Sajadieh, Ahmad, Haunsø, Stig, Svendsen, Jesper H, Olesen, Morten S
Publicado em 2013

Management of patients with Arrhythmogenic Right Ventricular Cardiomyopathy in the Nordic countries

Por Haugaa, Kristina H., Bundgaard, Henning, Edvardsen, Thor, Eschen, Ole, Gilljam, Thomas, Hansen, Jim, Jensen, Henrik Kjærulf, Platonov, Pyotr G., Svensson, Anneli, Svendsen, Jesper H.
Publicado no Scand Cardiovasc J (2015)

COPE-ICD: A randomised clinical trial studying the effects and meaning of a comprehensive rehabilitation programme for ICD recipients -design, intervention and population

Por Berg, Selina K, Svendsen, Jesper H, Zwisler, Ann-Dorthe, Pedersen, Birthe D, Preisler, Pernille, Siersbæk-Hansen, Lone, Hansen, Mette B, Nielsen, Rune H, Pedersen, Preben U
Publicado em 2011

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

Por Olesen, Morten S, Bentzen, Bo H, Nielsen, Jonas B, Steffensen, Annette B, David, Jens-Peter, Jabbari, Javad, Jensen, Henrik K, Haunsø, Stig, Svendsen, Jesper H, Schmitt, Nicole
Publicado em 2012

Risk prediction of cardiovascular death based on the QTc interval: evaluating age and gender differences in a large primary care population

Por Nielsen, Jonas B., Graff, Claus, Rasmussen, Peter V., Pietersen, Adrian, Lind, Bent, Olesen, Morten S., Struijk, Johannes J., Haunsø, Stig, Svendsen, Jesper H., Køber, Lars, Gerds, Thomas A., Holst, Anders G.
Publicado em 2014

Brugada syndrome risk loci seem protective against atrial fibrillation

Por Andreasen, Laura, Nielsen, Jonas B, Darkner, Stine, Christophersen, Ingrid E, Jabbari, Javad, Refsgaard, Lena, Thiis, Jens J, Sajadieh, Ahmad, Tveit, Arnljot, Haunsø, Stig, Svendsen, Jesper H, Schmitt, Nicole, Olesen, Morten S
Publicado no Eur J Hum Genet (2014)

Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes

Por Andreasen, Laura, Ahlberg, Gustav, Tang, Chuyi, Andreasen, Charlotte, Hartmann, Jacob P., Tfelt-Hansen, Jacob, Behr, Elijah R., Pehrson, Steen, Haunsø, Stig, LuCamp, Weeke, Peter E., Jespersen, Thomas, Olesen, Morten S., Svendsen, Jesper H.
Publicado no Eur J Hum Genet (2018)

Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest

Por Andreasen, Laura, Ghouse, Jonas, Skov, Morten W., Have, Christian T., Ahlberg, Gustav, Rasmussen, Peter V., Linneberg, Allan, Pedersen, Oluf, Platonov, Pyotr G., Haunsø, Stig, Svendsen, Jesper H., Hansen, Torben, Kanters, Jørgen K., Olesen, Morten S.
Publicado no Front Physiol (2018)

Gain of function in I(Ks) secondary to a mutation in KCNE5 associated with atrial fibrillation

Por Ravn, Lasse S., Aizawa, Yoshiyasu, Pollevick, Guido D., Hofman-Bang, Jacob, Cordeiro, Jonathan M., Dixen, Ulrik, Jensen, Gorm, Wu, Yuesheng, Burashnikov, Elena, Haunso, Stig, Guerchicoff, Alejandra, Hu, Dan, Svendsen, Jesper H., Christiansen, Michael, Antzelevitch, Charles
Publicado em 2008

Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation

Por Jabbari, Javad, Olesen, Morten S., Yuan, Lei, Nielsen, Jonas B., Liang, Bo, Macri, Vincenzo, Christophersen, Ingrid E., Nielsen, Nikolaj, Sajadieh, Ahmad, Ellinor, Patrick T., Grunnet, Morten, Haunsø, Stig, Holst, Anders G., Svendsen, Jesper H., Jespersen, Thomas
Publicado no Circ Cardiovasc Genet (2015)

Risk Prediction of Atrial Fibrillation Based on Electrocardiographic Interatrial Block

Por Skov, Morten W., Ghouse, Jonas, Kühl, Jørgen T., Platonov, Pyotr G., Graff, Claus, Fuchs, Andreas, Rasmussen, Peter V., Pietersen, Adrian, Nordestgaard, Børge G., Torp‐Pedersen, Christian, Hansen, Steen M., Olesen, Morten S., Haunsø, Stig, Køber, Lars, Gerds, Thomas A., Kofoed, Klaus F., Svendsen, Jesper H., Holst, Anders G., Nielsen, Jonas B.
Publicado no J Am Heart Assoc (2018)

Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development

Por Nielsen, Jonas B., Fritsche, Lars G., Zhou, Wei, Teslovich, Tanya M., Holmen, Oddgeir L., Gustafsson, Stefan, Gabrielsen, Maiken E., Schmidt, Ellen M., Beaumont, Robin, Wolford, Brooke N., Lin, Maoxuan, Brummett, Chad M., Preuss, Michael H., Refsgaard, Lena, Bottinger, Erwin P., Graham, Sarah E., Surakka, Ida, Chu, Yunhan, Skogholt, Anne Heidi, Dalen, Håvard, Boyle, Alan P., Oral, Hakan, Herron, Todd J., Kitzman, Jacob, Jalife, José, Svendsen, Jesper H., Olesen, Morten S., Njølstad, Inger, Løchen, Maja-Lisa, Baras, Aris, Gottesman, Omri, Marcketta, Anthony, O’Dushlaine, Colm, Ritchie, Marylyn D., Wilsgaard, Tom, Loos, Ruth J.F., Frayling, Timothy M., Boehnke, Michael, Ingelsson, Erik, Carey, David J., Dewey, Frederick E., Kang, Hyun M., Abecasis, Gonçalo R., Hveem, Kristian, Willer, Cristen J.
Publicado no Am J Hum Genet (2018)

Integrating Genetic, Transcriptional, and Functional Analyses to Identify Five Novel Genes for Atrial Fibrillation

Por Sinner, Moritz F., Tucker, Nathan R., Lunetta, Kathryn L., Ozaki, Kouichi, Smith, J. Gustav, Trompet, Stella, Bis, Joshua C., Lin, Honghuang, Chung, Mina K., Nielsen, Jonas B., Lubitz, Steven A., Krijthe, Bouwe P., Magnani, Jared W., Ye, Jiangchuan, Gollob, Michael H., Tsunoda, Tatsuhiko, Müller-Nurasyid, Martina, Lichtner, Peter, Peters, Annette, Dolmatova, Elena, Kubo, Michiaki, Smith, Jonathan D., Psaty, Bruce M., Smith, Nicholas L., Jukema, J. Wouter, Chasman, Daniel I., Albert, Christine M., Ebana, Yusuke, Furukawa, Tetsushi, MacFarlane, Peter, Harris, Tamara B., Darbar, Dawood, Dörr, Marcus, Holst, Anders G., Svendsen, Jesper H., Hofman, Albert, Uitterlinden, Andre G., Gudnason, Vilmundur, Isobe, Mitsuaki, Malik, Rainer, Dichgans, Martin, Rosand, Jonathan, Van Wagoner, David R., Benjamin, Emelia J., Milan, David J., Melander, Olle, Heckbert, Susan R., Ford, Ian, Liu, Yongmei, Barnard, John, Olesen, Morten S., Stricker, Bruno H.C., Tanaka, Toshihiro, Kääb, Stefan, Ellinor, Patrick T.
Publicado em 2014