Laura Andreasen
Laura Andreasen
MD, PhD student, Rigshospitalet, University Hospital of Copenhagen, Denmark
Bekræftet mail på regionh.dk
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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
2022013
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
502014
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
262018
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
172017
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
132015
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
132014
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
112013
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
52018
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
42017
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
32020
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
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
12020
Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis
L Andreasen, L Bertelsen, J Ghouse, PR Lundegaard, G Ahlberg, ...
Scientific Reports 10 (1), 1-8, 2020
2020
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
2020
4259 Discovery of the first genome-wide significant risk loci for syncope and collapse
G Ahlberg, K Hadji-Turdeghal, L Andreasen, CM Hagen, J Ghouse, ...
European Heart Journal 40 (Supplement_1), ehz745. 0137, 2019
2019
Titin-truncating variants associates with atrial fibrillation, compromises assembly of the sarcomere
MS Olesen, P Lundegaard, G Ahlberg, L Refsgaard, L Andreasen, ...
EUROPEAN HEART JOURNAL 39, 16-16, 2018
2018
195 Titin-truncating variants associates with atrial fibrillation, compromises assembly of the sarcomere
MS Olesen, P Lundegaard, G Ahlberg, L Refsgaard, L Andreasen, ...
European Heart Journal 39 (suppl_1), ehy564. 195, 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
Spectrum and prevalence of rare mutations involving 13 susceptible genes associated with AF in a cohort of unrelated early-onset lone AF patients
MS Olesen, L Andreasen, JB Nielsen, AG Holst, J Jabbari, SP Olesen, ...
European Heart Journal 34 (suppl_1), 2013
2013
Hereditary Atrial Fibrillation
L Andreasen
2013
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