Personal profile
Expertises
Cardiology; Genetics; Inherited cardioarrhythmia; Long QT syndrome; Electrocardiogram
Main research areas
Genetics within cardiac arrhythmia.
Current research
Currently, I am working on a genome wide association study, where we link the morphology of the T-wave on the electrocardiogram, with common variants in a study sample drawn from the general population. In total, we have enrolled roughly 6000 participants. Also, by employing epidemiological data provided by the Copenhagen ECG study, we are able to link the T-wave morphology with all-cause mortality and cardiovascular mortality.
Potential conflicts of interest
None
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Collaborations and top research areas from the last five years
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Association between IL-6 and hs-CRP and Cardiovascular Risk in Clinically Relevant Subgroups
Bundgaard, J. S., Ahlberg, G., Rand, S. A., Lundegaard, P. R., Stender, S., Vilhjálmsson, B. J., Kaspersen, K. A., Larsen, O. H., Schmidt, R. F., Bundgaard, H., Erikstrup, C. & Ghouse, J., 5 Mar 2026, (E-pub ahead of print) In: European Journal of Preventive Cardiology.Research output: Contribution to journal › Journal article › Research › peer-review
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Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Small, A. M., Yang, T.-Y., Itoh, S., Thériault, S., Dufresne, L., Kurosawa, R., Komuro, I., Matsuda, K., Vy, H. M. T., Farber-Eger, E. H., Shaffer, L. L., Boulier, K. M., Corey, K. M., Ramaker, M. E., Laporte, F., Schott, J.-J., Le Scouarnec, S., Singh, S. A., Sonawane, A. R. & Smith, H. A. & 34 others, , Jan 2026, In: Nature Genetics. 58, 1, p. 57-66 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
1 Citation (Scopus) -
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy
Nicastro, M., Vermeer, A. M. C., Postema, P. G., Tadros, R., Bowling, F. Z., Aegisdottir, H. M., Tragante, V., Mach, L., Postma, A. V., Lodder, E. M., van Duijvenboden, K., Zwart, R., Beekman, L., Wu, L., Jurgens, S. J., van der Zwaag, P. A., Alders, M., Allouba, M., Aguib, Y. & Santome, J. L. & 51 others, , 3 Jul 2025, In: American Journal of Human Genetics. 112, 7, p. 1681-1698 18 p.Research output: Contribution to journal › Journal article › Research › peer-review
1 Citation (Scopus) -
Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndrome
Christensen, A. H., Pan, G., Marvig, R. L., Rodriguez Gonzalez, F. G., Vissing, C. R., Silajdzija, E., Frosted, R., Girma, E. G., Gabrielaite, M., Jensen, H. K., Rossing, K., Henriksen, F. L., Sandgaard, N. C. F., Ahlberg, G., Ghouse, J., Lundegaard, P. R., Weischenfeldt, J., Wadelius, C. & Bundgaard, H., 15 Sept 2025, In: European Heart Journal. 46, 35, p. 3486-3497 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
6 Citations (Scopus) -
Genome-wide association study and polygenic risk prediction of hypothyroidism
Rand, S. A., Ahlberg, G., Tragante, V., Monfort, L. M., Zheng, C., Feldt-Rasmussen, U., Klose, M. C., Teder-Laving, M., Metspalu, A., Poulsen, H. E., Ellervik, C., Nygaard, B., Erikstrup, C., Bruun, M. T., A Jensen, B., Ullum, H., Brunak, S., Schwinn, M., Ostrowski, S. R. & Pedersen, O. B. & 11 others, , Dec 2025, In: Nature Genetics. 57, 12, p. 3007-3015 9 p.Research output: Contribution to journal › Journal article › Research › peer-review