Laura Andreasen
Laura Andreasen
MD, PhD student, Rigshospitalet, University Hospital of Copenhagen, Denmark
Verified email at regionh.dk
Title
Cited by
Cited by
Year
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants
C Andreasen, JB Nielsen, L Refsgaard, AG Holst, AH Christensen, ...
European Journal of Human Genetics 21 (9), 918-928, 2013
2162013
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
602014
Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation
G Ahlberg, L Refsgaard, PR Lundegaard, L Andreasen, MF Ranthe, ...
Nature communications 9 (1), 1-11, 2018
492018
Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality
J Ghouse, CT Have, MW Skov, L Andreasen, G Ahlberg, JB Nielsen, ...
Genetics in Medicine 19 (5), 521-528, 2017
212017
Genetic aspects of lone atrial fibrillation: what do we know?
L Andreasen, J B Nielsen, M S Olesen
Current pharmaceutical design 21 (5), 667-678, 2015
152015
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
152014
Genetic modifier of the QTc interval associated with early-onset atrial fibrillation
L Andreasen, JB Nielsen, IE Christophersen, AG Holst, A Sajadieh, ...
Canadian Journal of Cardiology 29 (10), 1234-1240, 2013
122013
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes
L Andreasen, G Ahlberg, C Tang, C Andreasen, JP Hartmann, ...
European Journal of Human Genetics 26 (5), 660-668, 2018
82018
Loss-of-function variants in cytoskeletal genes are associated with early-onset atrial fibrillation
OB Vad, C Paludan-Müller, G Ahlberg, SM Kalstø, J Ghouse, L Andreasen, ...
Journal of clinical medicine 9 (2), 372, 2020
72020
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
72017
Genome-wide association study identifies locus at chromosome 2q32. 1 associated with syncope and collapse
K Hadji-Turdeghal, L Andreasen, CM Hagen, G Ahlberg, J Ghouse, ...
Cardiovascular research 116 (1), 138-148, 2020
62020
Atrial fibrillation—a complex polygenetic disease
JH Andersen, L Andreasen, MS Olesen
European Journal of Human Genetics, 1-10, 2020
22020
Verification of threshold for image intensity ratio analyses of late gadolinium enhancement magnetic resonance imaging of left atrial fibrosis in 1.5 T scans
L Bertelsen, F Alarcón, L Andreasen, E Benito, MS Olesen, N Vejlstrup, ...
The international journal of cardiovascular imaging 36 (3), 513-520, 2020
22020
Brugada syndrome-associated genetic loci are associated with J-point elevation and an increased risk of cardiac arrest
L Andreasen, J Ghouse, MW Skov, CT Have, G Ahlberg, PV Rasmussen, ...
Frontiers in physiology 9, 894, 2018
22018
Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors
J Ghouse, G Ahlberg, L Andreasen, K Banasik, S Brunak, M Schwinn, ...
Journal of the American College of Cardiology 78 (7), 696-709, 2021
12021
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function
G Ahlberg, L Andreasen, J Ghouse, L Bertelsen, H Bundgaard, S Haunsø, ...
European Heart Journal, 2021
12021
Cardiac magnetic resonance systematically overestimates mitral regurgitations by the indirect method
L Bertelsen, N Vejlstrup, L Andreasen, MS Olesen, JH Svendsen
Open heart 7 (2), e001323, 2020
12020
Mendelian randomization—a powerful tool to study the causal effects of atrial fibrillation on loss of brain volume
L Andreasen
BMC medicine 19 (1), 1-2, 2021
2021
Rare coding variants in MYH6 are associated with atrial fibrillation: results from 45,596 exomes representing the general population
OB Vad, C Paludan-Muller, G Ahlberg, L Andreasen, L Refsgaard, ...
European Heart Journal 41 (Supplement_2), ehaa946. 0342, 2020
2020
Genome-wide association study of patients with atrioventricular nodal reentry tachycardia
L Andreasen, G Ahlberg, J Hartmann, C Paludan-Mueller, HK Jensen, ...
European Heart Journal 41 (Supplement_2), ehaa946. 3687, 2020
2020
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