Screening of the I(to) Regulatory Subunit Klf15 in Patients with Early-Onset Lone Atrial Fibrillation

Por Nielsen, Morten Wagner, Olesen, Morten Salling, Refsgaard, Lena, Haunsø, Stig, Svendsen, Jesper Hastrup
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

Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy

Por Refsgaard, Lena, Olesen, Morten Salling, Møller, Daniel Vega, Christiansen, Michael, Haunsø, Stig, Svendsen, Jesper Hastrup, Christensen, Alex Hørby
Publicado no Appl Transl Genom (2012)

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

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)

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)