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Oliver Bundgaard Vad
Oliver Bundgaard Vad
M.D., PhD fellow; Department of Cardiology, Rigshospitalet, Copenhagen University Hospital
Verified email at sund.ku.dk
Title
Cited by
Cited by
Year
Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation
AG Clausen, OB Vad, JH Andersen, MS Olesen
Frontiers in cardiovascular medicine 8, 650667, 2021
192021
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
192020
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts
C Paludan-Müller, J Ghouse, OB Vad, CB Herfelt, P Lundegaard, ...
European Journal of Human Genetics 27 (9), 1427-1435, 2019
112019
A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation
TH Hansen, Y Yan, G Ahlberg, OB Vad, L Refsgaard, JL Dos Santos, ...
Scientific Reports 10 (1), 1453, 2020
92020
Evident decline in mortality from ischaemic heart disease in Denmark from 1970 to 2015
S Haunsø, OB Vad, O Amtorp
Ugeskrift for laeger 182 (37), V02200113, 2020
62020
Loss of cardiac splicing regulator RBM20 is associated with early-onset atrial fibrillation
OB Vad, E Angeli, M Liss, G Ahlberg, L Andreasen, IE Christophersen, ...
JACC: Basic to Translational Science 9 (2), 163-180, 2024
32024
Dramatisk fald i hjertedødelighed i Danmark fra 1970 til 2015
S Haunsø, OB Vad, O Amtorp
Ugeskr Læger 182, V02200113, 2020
32020
CineECG analysis provides new insights into Familial ST-segment Depression Syndrome
R Frosted, C Paludan-Müller, OB Vad, MS Olesen, H Bundgaard, ...
Europace 25 (5), euad116, 2023
22023
Loss-of-function variants in founder population highlight atrial myopathy as susceptibility to atrial fibrillation
C Paludan-Muller, OB Vad, K Kahnert, G Ahlberg, LM Monfort, SA Rand, ...
European Heart Journal 43 (Supplement_2), ehac544. 2875, 2022
12022
Whole-exome sequencing implicates neuronal calcium channel with familial atrial fibrillation
OB Vad, Y Yan, F Denti, G Ahlberg, L Refsgaard, SH Bomholtz, JL Santos, ...
Frontiers in Genetics, 5, 2022
12022
Atrial fibrillation: age at diagnosis, incident cardiovascular events, and mortality
C Paludan-Müller, OB Vad, NK Stampe, SZ Diederichsen, L Andreasen, ...
European Heart Journal, ehae216, 2024
2024
Accessory Pathway Treated With Catheter Ablation Is Associated With Cardiomyopathy, Heart Failure, and Mortality
C Paludan-Müller, NK Stampe, OB Vad, L Andreasen, C Torp-Pedersen, ...
Clinical Electrophysiology, 2024
2024
Tackling a growing healthcare challenge: atrial fibrillation epidemiology, prevention, and underlying causes
OB Vad, C Paludan-Müller, SZ Diederichsen, MS Olesen
The Lancet Regional Health–Europe 37, 2024
2024
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death
C Paludan‐Müller, NK Stampe, LM Monfort, L Andreasen, OB Vad, ...
Journal of the American Heart Association, e034439, 2024
2024
Unlocking the genetic code: Novel insights into familial atrial fibrillation and gene-variant interactions
OB Vad, MS Olesen
The Canadian journal of cardiology, S0828-282X (23) 01963-3, 2023
2023
Genetically predicted adipose tissue distribution influences the risk of atherosclerosis
OB Vad, C Paludan-Müller, LM Monfort, G Ahlberg, JH Svendsen, ...
European Journal of Preventive Cardiology 30 (7), e41-e45, 2023
2023
Genome-wide association study of atrial fibrillation in 114,539 Finnish individuals reveals novel locus associated with cardiac remodelling
C Paludan-Muller, OB Vad, JH Svendsen, MS Olesen
European Heart Journal 42 (Supplement_1), ehab724. 3322, 2021
2021
Integration of Scandinavian genetic data with UK biobank data implicates the RBM20 gene with atrial fibrillation pathogenesis
OB Vad, E Angeli, M Liss, G Ahlberg, L Andreasen, IE Christophersen, ...
European Heart Journal 42 (Supplement_1), ehab724. 3319, 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
Rare variants in HCN4 identified in the general population are associated with complete atrioventricular (AV) block, 1. degree AV block and bundle branch block, results from 50 …
J Jensen, OB Vad, C Paludan-Muller, PR Lundegaard, JH Svendsen, ...
European Heart Journal 41 (Supplement_2), ehaa946. 3588, 2020
2020
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