Olesen, Morten Salling

Top Publications

Top Publications Authored or Co-Authored by "Olesen, Morten Salling"

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

  Nature Genetics, Volume 45, No. 9, Year 2013, Citations 480
• High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation

  Circulation: Cardiovascular Genetics, Volume 5, No. 4, Year 2012, Citations 131
• Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

  Cardiovascular Research, Volume 89, No. 4, Year 2011, Citations 126
• Role of common and rare variants in SCN10A: Results from the Brugada syndrome QRS locus gene discovery collaborative study

  Cardiovascular Research, Volume 106, No. 3, Year 2015, Citations 118
• Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse

  Cardiovascular Research, Volume 116, No. 1, Year 2020, Citations 13