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Oliver Bundgaard Vad
Oliver Bundgaard Vad
M.D., PhD fellow; Department of Cardiology, Rigshospitalet, Copenhagen University Hospital
在 sund.ku.dk 的电子邮件经过验证
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引用次数
引用次数
年份
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
202020
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
182021
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
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
52024
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
Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk
OB Vad, LM Monfort, C Paludan-Müller, K Kahnert, SZ Diederichsen, ...
JAMA cardiology, 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 13 (9), e034439, 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 10 (5), 973-975, 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
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
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