| Stability of circulating blood-based microRNAs–pre-analytic methodological considerations C Glinge, S Clauss, K Boddum, R Jabbari, J Jabbari, B Risgaard, ... PloS one 12 (2), e0167969, 2017 | 355 | 2017 |
| Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study ER Behr, E Savio-Galimberti, J Barc, AG Holst, E Petropoulou, BP Prins, ... Cardiovascular research 106 (3), 520-529, 2015 | 132 | 2015 |
| Incidence and risk factors of ventricular fibrillation before primary angioplasty in patients with first ST‐elevation myocardial infarction: a nationwide study in Denmark R Jabbari, T Engstrøm, C Glinge, B Risgaard, J Jabbari, BG Winkel, ... Journal of the American Heart Association 4 (1), e001399, 2015 | 131 | 2015 |
| Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation MS Olesen, BH Bentzen, JB Nielsen, AB Steffensen, JP David, J Jabbari, ... BMC medical genetics 13, 1-9, 2012 | 114 | 2012 |
| New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia J Jabbari, R Jabbari, MW Nielsen, AG Holst, JB Nielsen, S Haunsø, ... Circulation: Cardiovascular Genetics 6 (5), 481-489, 2013 | 89 | 2013 |
| Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation J Jabbari, MS Olesen, L Yuan, JB Nielsen, B Liang, V Macri, ... Circulation: Cardiovascular Genetics 8 (1), 64-73, 2015 | 87 | 2015 |
| Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years MS Olesen, AG Holst, J Jabbari, JB Nielsen, IE Christophersen, ... Canadian Journal of Cardiology 28 (2), 191-195, 2012 | 79 | 2012 |
| Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation MS Olesen, L Andreasen, J Jabbari, L Refsgaard, S Haunsø, SP Olesen, ... Heart Rhythm 11 (2), 246-251, 2014 | 74 | 2014 |
| Rare variants in GJA5 are associated with early-onset lone atrial fibrillation IE Christophersen, HN Holmegard, J Jabbari, S Haunsø, A Tveit, ... Canadian Journal of Cardiology 29 (1), 111-116, 2013 | 61 | 2013 |
| Screening of KCNN3 in patients with early-onset lone atrial fibrillation MS Olesen, J Jabbari, AG Holst, JB Nielsen, DA Steinbrüchel, ... Europace 13 (7), 963-967, 2011 | 55 | 2011 |
| Common Polymorphisms in KNCJ5 Are Associated with Early-Onset Lone Atrial Fibrillation in Caucasians J Jabbari, MS Olesen, AG Holst, JB Nielsen, S Haunso, JH Svendsen Cardiology 118 (2), 116-120, 2011 | 33 | 2011 |
| A common variant in SCN5A and the risk of ventricular fibrillation caused by first ST-segment elevation myocardial infarction R Jabbari, C Glinge, J Jabbari, B Risgaard, BG Winkel, CJ Terkelsen, ... PLoS One 12 (1), e0170193, 2017 | 25 | 2017 |
| New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome RQ Yang, J Jabbari, XS Cheng, R Jabbari, JB Nielsen, B Risgaard, ... BMC genetics 15, 1-8, 2014 | 20 | 2014 |
| Brugada syndrome risk loci seem protective against atrial fibrillation L Andreasen, JB Nielsen, S Darkner, IE Christophersen, J Jabbari, ... European Journal of Human Genetics 22 (12), 1357-1361, 2014 | 16 | 2014 |
| Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants E Gregers, G Ahlberg, T Christensen, J Jabbari, KO Larsen, CB Herfelt, ... Heart Rhythm 14 (10), 1531-1538, 2017 | 13 | 2017 |
| The pathogenicity of genetic variants previously associated with left ventricular non‐compaction Y Abbasi, J Jabbari, R Jabbari, RQ Yang, B Risgaard, L Køber, S Haunsø, ... Molecular Genetics & Genomic Medicine 4 (2), 135-142, 2016 | 9 | 2016 |
| Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction R Jabbari, J Jabbari, C Glinge, B Risgaard, S Sattler, BG Winkel, ... BMC Medical Genetics 18, 1-6, 2017 | 4 | 2017 |
| Exome data clouds the pathogenicity of genetic variants in Pulmonary Arterial Hypertension Y Abbasi, J Jabbari, R Jabbari, C Glinge, SB Izadyar, E Spiekerkoetter, ... Molecular Genetics & Genomic Medicine 6 (5), 835-844, 2018 | 3 | 2018 |
| Patients with valvular heart disease and atrial fibrillation carry a high number of germline mutations E Gregers, GA Ahlberg, KO Larsen, J Jabbari, CB Herfelt, KM Henningsen, ... EUROPEAN HEART JOURNAL 37, 302-302, 2016 | | 2016 |
| Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation (vol 8, pg 64, 2015) J Jabbari, MS Olesen, L Yuan CIRCULATION-CARDIOVASCULAR GENETICS 9 (1), 100-100, 2016 | | 2016 |
Jesper Hastrup SvendsenProfessor, MD, DMSc, FESC, FEHRAVerificeret mail på regionh.dk
