Research output per year
Research output per year
- 17 results
Search results
-
2024
Atrial fibrillation: age at diagnosis, incident cardiovascular events, and mortality
Paludan-Müller, C., Vad, O. B., Stampe, N. K., Diederichsen, S. Z., Andreasen, L., Monfort, L. M., Fosbøl, E. L., Køber, L., Torp-Pedersen, C., Svendsen, J. H. & Olesen, M. S., 2024, In: European Heart Journal. 45, 24, p. 2119-2129 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile11 Citations (Scopus)9 Downloads (Pure) -
Genetic Determinants of Left Atrial Function Are Associated With Stroke
Vad, O. B., Paludan-Müller, C., Diederichsen, S. Z., McKaige, E. A., Monfort, L. M., Lundegaard, P. R., Bertelsen, L., Andreasen, L., Svendsen, J. H. & Olesen, M. S., 2024, In: Journal of the American Heart Association. 13, 23, 13 p., e037490.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile -
Genetic Susceptibility to Hidradenitis Suppurativa and Predisposition to Cardiometabolic Disease
Nielsen, V. W., Vad, O. B., Holgersen, N., Paludan-Müller, C., Monfort, L. M., Beyer, A. F., Jemec, G. B. E., Kjærsgaard Andersen, R., Egeberg, A., Thyssen, J. P., Svendsen, J. H., Rosenø, N. A. L., Hansen, P. R., Thomsen, S. F. & Salling Olesen, M., 9 Oct 2024, (E-pub ahead of print) In: JAMA Dermatology. 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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 others, , 4 Sep 2024, (E-pub ahead of print) In: JAMA Cardiology.Research output: Contribution to journal › Journal article › Research › peer-review
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Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death
Paludan-Müller, C., Stampe, N. K., Monfort, L. M., Andreasen, L., Vad, O. B., Ahlberg, G., Johansen, J. B., Winkel, B. G., Torp-Pedersen, C., Køber, L., Fosbøl, E. L., Svendsen, J. H. & Olesen, M. S., 2024, In: Journal of the American Heart Association. 13, 9, 4 p., e034439.Research output: Contribution to journal › Letter › Research › peer-review
Open AccessFile13 Downloads (Pure) -
Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk
Vad, O. B., Monfort, L. M., Paludan-Müller, C., Kahnert, K., Diederichsen, S. Z., Andreasen, L., Lotta, L. A., Nielsen, J. B., Lundby, A., Svendsen, J. H., Olesen, M. S. & Geisinger MyCode Community Health Initiative and the Regeneron Genetics Center (RGC) Research Team, 2024, In: JAMA Cardiology. 9, 8, p. 732-740 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile3 Citations (Scopus)6 Downloads (Pure) -
Tackling a growing healthcare challenge: atrial fibrillation epidemiology, prevention, and underlying causes
Vad, O. B., Paludan-Müller, C., Diederichsen, S. Z. & Olesen, M. S., 2024, In: The Lancet Regional Health - Europe. 37, 2 p., 100827.Research output: Contribution to journal › Comment/debate › Research › peer-review
Open AccessFile1 Citation (Scopus)10 Downloads (Pure) -
2023
CineECG analysis provides new insights into Familial ST-segment Depression Syndrome
Frosted, R., Paludan-Mueller, C., Vad, O. B., Olesen, M. S., Bundgaard, H., van Dam, P. & Christensen, A. H., 2023, In: Europace. 25, 5, 11 p., euad116.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile2 Citations (Scopus)22 Downloads (Pure) -
Genetically predicted adipose tissue distribution influences the risk of atherosclerosis
Vad, O. B., Paludan-Müller, C., Monfort, L. M., Ahlberg, G., Svendsen, J. H. & Olesen, M. S., 2023, In: European Journal of Preventive Cardiology. 30, 7, p. e41–e45Research output: Contribution to journal › Letter › Research › peer-review
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2022
Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population.
Paludan-Müller, C., Larsen, S., Ahlberg, G., Monfort, L. M., Andreasen, L., Svendsen, J. H., Jespersen, T., Bundgaard, H., Kanters, J. K. & Olesen, M. S., 2022, In: Circulation. Genomic and precision medicine. 15, 1, p. 83-85 3 p., e003574.Research output: Contribution to journal › Letter › Research › peer-review
Open AccessFile8 Downloads (Pure) -
Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT
Andreasen, L., Ahlberg, G., Ægisdóttir, H. M., Sveinbjörnsson, G., Lundegaard, P. R., Hartmann, J. P., Paludan-Müller, C., Hadji-Turdeghal, K., Ghouse, J., Pehrson, S., Jensen, H. K., Riahi, S., Hansen, J., Sandgaard, N., Sørensen, E., Banasik, K., Sækmose, S. G., Bruun, M. T., Hjalgrim, H., Erikstrup, C. & 18 others, , 2022, In: Circulation Research. 131, 10, p. 862-865Research output: Contribution to journal › Letter › Research › peer-review
4 Citations (Scopus) -
2020
Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation
Vad, O. B., Paludan-Mueller, C., Ahlberg, G., Kalsto, S. M., Ghouse, J., Andreasen, L., Haunso, S., Tveit, A., Sajadieh, A., Christophersen, I. E., Svendsen, J. H. & Olesen, M. S., 2020, In: Journal of Clinical Medicine. 9, 2, 12 p., 372.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile14 Citations (Scopus)90 Downloads (Pure) -
2019
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts
Paludan-Mueller, C., Ghouse, J., Vad, O. B., Herfelt, C. B., Lundegaard, P., Ahlberg, G., Schmitt, N., Svendsen, J. H., Haunso, S., Bundgaard, H., Hansen, T., Kanters, J. K. & Olesen, M. S., 2019, In: European Journal of Human Genetics. 27, 9, p. 1427-1435Research output: Contribution to journal › Journal article › Research › peer-review
Open Access7 Citations (Scopus) -
2018
Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation
Denti, F., Paludan-Müller, C., Olesen, S-P., Haunsø, S., Svendsen, J. H., Olesen, M. S., Bentzen, B. H. & Schmitt, N., Mar 2018, In: Personalized Medicine. 15, 2, p. 93-102 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
4 Citations (Scopus) -
2017
Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease
Paludan-Müller, C., Ahlberg, G., Ghouse, J., Svendsen, J. H., Haunsø, S. & Olesen, M. S., 2017, In: Circulation. Cardiovascular genetics. 10, 6, 10 p., e001878.Research output: Contribution to journal › Journal article › Research › peer-review
7 Citations (Scopus) -
Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants
Paludan-Müller, C., Ahlberg, G., Ghouse, J., Herfelt, C., Svendsen, J. H., Haunsø, S., Kanters, J. K. & Olesen, M. S., Jan 2017, In: Clinical Genetics. 91, 1, p. 63–72Research output: Contribution to journal › Journal article › Research › peer-review
32 Citations (Scopus) -
2016
The role of common genetic variants in atrial fibrillation
Paludan-Müller, C., Svendsen, J. H. & Olesen, M. S., 2016, In: Journal of Electrocardiology. 49, 6, p. 864-870Research output: Contribution to journal › Journal article › Research › peer-review
20 Citations (Scopus)