Jonas Ghouse

Publikationer pr. år

Expertise

Cardiology; Genetics; Inherited cardioarrhythmia; Long QT syndrome; Electrocardiogram

Primære forskningsområder

Genetics within cardiac arrhythmia.

Aktuel forskning

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.

Mulige interessekonflikter

None

Fingeraftryk

Dyk ned i forskningsemnerne, hvor Jonas Ghouse er aktive. Disse emneetiketter kommer fra denne persons arbejder. Sammen danner de et unikt fingerprint.

6 Lignende profiler

43 Tidsskriftartikel
2 Letter
1 Ph.d.-afhandling
1 Preprint

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Henry, A., Mo, X., Finan, C., Chaffin, M. D., Speed, D., Issa, H., Denaxas, S., Ware, J. S., Zheng, S. L., Malarstig, A., Gratton, J., Bond, I., Roselli, C., Miller, D., Chopade, S., Schmidt, A. F., Abner, E., Adams, L., Andersson, C. & Aragam, K. G. & 31 flere, Ärnlöv, J., Asselin, G., Raja, A. A., Backman, J. D., Bartz, T. M., Biddinger, K. J., Biggs, M. L., Bloom, H. L., Boersma, E., Brandimarto, J., Brown, M. R., Brunak, S., Bruun, M. T., Buckbinder, L., Bundgaard, H., Carey, D. J., Chasman, D. I., Chen, X., Dowsett, J., Ghouse, J., Køber, L., Ostrowski, S. R., Pedersen, O. B., Sørensen, E., Torp-Pedersen, C., Ullum, H., Vissing, C. R., Weeke, P. E., Zannad, F., Zheng, C. & Genes & Health Research Team, 4 mar. 2025, (E-pub ahead of print) I: Nature Genetics.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
Genome-Wide Association Study of Plasma Sodium Concentrations with and without Exposure to Thiazide Diuretics
Andersson, N. W., Wu, X., Geller, F., Wohlfahrt, J., Melbye, M., Hviid, A., Schwinn, M., Mikkelsen, C., Dowsett, J., Bruun, M. T., Aagaard, B., Ullum, H., Erikstrup, C., Gudbjartsson, D. F., Stefánsson, K., Ghouse, J., Pedersen, O. B., Sørensen, E., Ostrowski, S. R. & Bundgaard, H. & 3 flere, Lund, M., Feenstra, B. & DBDS Genomic Consortium, 31 jan. 2025, (E-pub ahead of print) I: Journal of the American Society of Nephrology : JASN. 10.1681/ASN.0000000622.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable 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., van der Zwaag, P. A., Alders, M., Allouba, M., Aguib, Y., Santomel, J. L. & de Una, D. & 50 flere, Monserrat, L., Miranda, A. M. A., Kanemaru, K., Cranley, J., van Zeggeren, I. E., Aronica, E. M. A., Ripolone, M., Zanotti, S., Sveinbjornsson, G., Ivarsdottir, E. V., Hólm, H., Guðbjartsson, D. F., Skúladóttir, Á. T., Stefánsson, K., Nadauld, L., Knowlton, K. U., Ostrowski, S. R., Sørensen, E., Vesterager Pedersen, O. B., Ghouse, J., Rand, S., Bundgaard, H., Ullum, H., Erikstrup, C., Aagaard, B., Bruun, M. T., Christiansen, M., Jensen, H. K., Carere, D. A., Cummings, C. T., Fishler, K., Tøring, P. M., Brusgaard, K., Juul, T. M., Saaby, L., Winkel, B. G., Mogensen, J., Fortunato, F., Comi, G. P., Ronchi, D., van Tintelen, J. P., Noseda, M., Airola, M. V., Christiaans, I., Wilde, A. A. M., Wilders, R., Clur, S.-A., Verkerk, A. O., Bezzina, C. R. & Lahrouchi, N., 5 jul. 2024, (medRxiv : the preprint server for health sciences).
Publikation: Working paper › Preprint
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Zheng, S. L., Henry, A., Cannie, D., Lee, M., Miller, D., McGurk, K. A., Bond, I., Xu, X., Issa, H., Francis, C., De Marvao, A., Theotokis, P. I., Buchan, R. J., Speed, D., Abner, E., Adams, L., Aragam, K. G., Ärnlöv, J., Raja, A. A. & Backman, J. D. & 31 flere, Baksi, J., Barton, P. J. R., Biddinger, K. J., Boersma, E., Brandimarto, J., Brunak, S., Bundgaard, H., Carey, D. J., Charron, P., Cook, J. P., Cook, S. A., Denaxas, S., Deleuze, J.-F., Doney, A. S., Elliott, P., Erikstrup, C., Esko, T., Farber-Eger, E. H., Finan, C., Garnier, S., Ghouse, J., Giedraitis, V., Guðbjartsson, D. F., Haggerty, C. M., Halliday, B. P., Helgadottir, A., Hemingway, H., Ostrowski, S. R., Pedersen, O. B. V., Ullum, H. & COVIDsortium, dec. 2024, I: Nature Genetics. 56, 12, s. 2646-2658 13 s., 2254.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
2 Citationer (Scopus)
Genome-Wide Association Study of Accessory Atrioventricular Pathways
Aegisdottir, H. M., Andreasen, L., Thorolfsdottir, R. B., Sveinbjornsson, G., Jonsdottir, A. B., Stefansdottir, L., Thorleifsson, G., Sigurdsson, A., Halldorsson, G. H., Barc, J., Simonet, F., Tragante, V., Oddsson, A., Ferkingstad, E., Svendsen, J. H., Ghouse, J., Ahlberg, G., Paludan-Müller, C., Hadji-Turdeghal, K. & Bustamante, M. & 24 flere, Ulfarsson, M. O., Helgadottir, A., Gretarsdottir, S., Saevarsdottir, S., Jonsdottir, I., Erikstrup, C., Ullum, H., Sørensen, E., Brunak, S., Jøns, C., Zheng, C., Bezzina, C. R., Knowlton, K. U., Nadauld, L. D., Sulem, P., Ostrowski, S. R., Pedersen, O. B., Arnar, D. O., Gudbjartsson, D. F., Olesen, M. S., Bundgaard, H., Holm, H., Stefansson, K. & DBDS Consortium, 1 nov. 2024, I: JAMA Cardiology. 9, 11, s. 1053-1058 6 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Jonas Ghouse

Personlig profil

Expertise

Primære forskningsområder

Aktuel forskning

Mulige interessekonflikter

Fingeraftryk

Samarbejde og topforskningsområder i de sidste fem år

Dyk ned i detaljerne

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes

Genome-Wide Association Study of Plasma Sodium Concentrations with and without Exposure to Thiazide Diuretics

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy

Genome-Wide Association Study of Accessory Atrioventricular Pathways