The genetic component of Brugada syndrome

Por Nielsen, Morten W., Holst, Anders G., Olesen, Søren-Peter, Olesen, Morten S.
Publicado em 2013

High prevalence of genetic variants previously associated with LQT syndrome in new exome data

Por Refsgaard, Lena, Holst, Anders G, Sadjadieh, Golnaz, Haunsø, Stig, Nielsen, Jonas B, Olesen, Morten S
Publicado em 2012

Effect of Semaglutide on the Pharmacokinetics of Metformin, Warfarin, Atorvastatin and Digoxin in Healthy Subjects

Por Hausner, Helene, Derving Karsbøl, Julie, Holst, Anders G., Jacobsen, Jacob B., Wagner, Frank-Dietrich, Golor, Georg, Anderson, Thomas W.
Publicado no Clin Pharmacokinet (2017)

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

A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease

Por Holst, Anders G., Calloe, Kirstine, Jespersen, Thomas, Cedergreen, Pernille, Winkel, Bo G., Jensen, Henrik Kjaerulf, Leren, Trond P., Haunso, Stig, Svendsen, Jesper Hastrup, Tfelt-Hansen, Jacob
Publicado em 2009

Vigorous physical activity impairs myocardial function in patients with arrhythmogenic right ventricular cardiomyopathy and in mutation positive family members

Por Saberniak, Jørg, Hasselberg, Nina E, Borgquist, Rasmus, Platonov, Pyotr G, Sarvari, Sebastian I, Smith, Hans-Jørgen, Ribe, Margareth, Holst, Anders G, Edvardsen, Thor, Haugaa, Kristina H
Publicado no Eur J Heart Fail (2014)

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

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)

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

Por Behr, Elijah R., Savio-Galimberti, Eleonora, Barc, Julien, Holst, Anders G., Petropoulou, Evmorfia, Prins, Bram P., Jabbari, Javad, Torchio, Margherita, Berthet, Myriam, Mizusawa, Yuka, Yang, Tao, Nannenberg, Eline A., Dagradi, Federica, Weeke, Peter, Bastiaenan, Rachel, Ackerman, Michael J., Haunso, Stig, Leenhardt, Antoine, Kääb, Stefan, Probst, Vincent, Redon, Richard, Sharma, Sanjay, Wilde, Arthur, Tfelt-Hansen, Jacob, Schwartz, Peter, Roden, Dan M., Bezzina, Connie R., Olesen, Morten, Darbar, Dawood, Guicheney, Pascale, Crotti, Lia, Jamshidi, Yalda
Publicado no Cardiovasc Res (2015)

Association of Traditional Cardiovascular Risk Factors with Venous Thromboembolism: An Individual Participant Data Meta-analysis of Prospective Studies

Por Mahmoodi, Bakhtawar K., Cushman, Mary, Næss, Inger Anne, Allison, Matthew A., Bos, Willem Jan, Brækkan, Sigrid K., Cannegieter, Suzanne C., Gansevoort, Ron T., Gona, Philimon N., Hammerstrøm, Jens, Hansen, John-Bjarne, Heckbert, Susan, Holst, Anders G., Lakoski, Susan G., Lutsey, Pamela L., Manson, JoAnn E., Martin, Lisa W., Matsushita, Kunihiro, Meijer, Karina, Overvad, Kim, Prescott, Eva, Puurunen, Marja, Rossouw, Jacques E., Sang, Yingying, Severinsen, Marianne T., Berg, Jur ten, Folsom, Aaron R., Zakai, Neil A.
Publicado no Circulation (2016)

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