Javad Jabbari
Javad Jabbari
Radiometer Medical, Denmark
Verified email at radiometer.dk
TitleCited byYear
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), 24, 2012
782012
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
762015
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
692017
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
682013
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
572015
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
512012
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
492013
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
482015
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
442014
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
432011
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
272011
Glioma spheroids obtained via ultrasonic aspiration are viable and express stem cell markers: a new tissue resource for glioma research
SS Jensen, C Aaberg-Jessen, C Andersen, HD Schrøder, BW Kristensen
Neurosurgery 73 (5), 868-886, 2013
242013
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), 74, 2014
132014
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
112017
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, 2014
112014
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
62016
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), 138, 2017
32017
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
32017
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
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
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