Morten S. Olesen

Genetic Misdiagnoses and the Potential for Health Disparities

Arjun K. Manrai, Birgit Funke, Heidi L. Rehm et al. · New England Journal of Medicine · 2016 · 804 citations · Full text

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Connie R. Bezzina, Julien Barc, Yuka Mizusawa et al. · Nature Genetics · 2013 · 540 citations · Full text

Cardiomyopathy, Genetic Disorder, Genetics +9

P-wave duration and the risk of atrial fibrillation: Results from the Copenhagen ECG Study

Jonas B. Nielsen, Jørgen Tobias Kühl, Adrian Pietersen et al. · Heart Rhythm · 2015 · 223 citations

Electrophysiological Evaluation, Cardiovascular Disease, Medicine +7

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

Charlotte Andreasen, Jonas B. Nielsen, Lena Refsgaard et al. · European Journal of Human Genetics · 2013 · 213 citations · Full text

Cardiomyopathy, Genetics, Pathology +5

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

Ingrid E. Christophersen, Morten S. Olesen, Bo Liang et al. · European Heart Journal · 2012 · 154 citations · Full text