Jørgen K. Kanters
Associate Professor
Physiology of circulation, kidney and lung
Blegdamsvej 3
2200 København N.
- Published
Normal electrocardiographic QT interval in race-fit Standardbred horses at rest and its rate dependence during exercise
Pedersen, P. J., Kanters, Jørgen K., Buhl, Rikke & Klærke, Dan Arne, Mar 2013, In: Journal of Veterinary Cardiology. 15, 1, p. 23-31 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
New descriptors of T-wave morphology are independent of heart rate
Andersen, M. P., Xue, J. Q., Graff, C., Kanters, Jørgen K., Toft, E. & Struijk, J. J., 2008, In: Journal of Electrocardiology. 41, 6, p. 557-61 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Neurocardiogenic syncope in long-QT syndrome is not necessarily benign
Kanters, Jørgen K., Thomsen, P. E. B., Christiansen, M. & Toft, E., 2006, In: Clinical Research in Cardiology. 95, 6, p. 349; author reply 350Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients.
Nielsen, N. H., Winkel, B. G., Kanters, Jørgen K., Schmitt, Nicole, Hofman-Bang, J., Jensen, H. S., Bentzen, Bo Hjorth, Sigurd, B., Larsen, Lars Allan, Andersen, P. S., Kjeldsen, K., Grunnet, Morten, Christiansen, M., Olesen, Søren-Peter & Haunsø, Stig, 2007, In: Biochemical and Biophysical Research Communications. 354, 3, p. 776-82 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome
Christiansen, M., Tonder, N., Larsen, L. A., Andersen, P. S., Simonsen, H., Oyen, N., Kanters, Jørgen K., Jacobsen, J. R., Fosdal, I., Wettrell, G. & Kjeldsen, K., 2005, In: American Journal of Cardiology. 95, p. 433-434Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndrome
Barsheshet, A., Goldenberg, I., O-Uchi, J., Moss, A. J., Jons, C., Shimizu, W., Wilde, A. A., McNitt, S., Peterson, D. R., Zareba, W., Robinson, J. L., Ackerman, M. J., Cypress, M., Gray, D. A., Hofman, N., Kanters, J. K., Kaufman, E. S., Platonov, P. G., Qi, M., Towbin, J. A. & 2 others, , 24 Apr 2012, In: Circulation. 125, 16, p. 1988-96 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome
Jons, C., Moss, A. J., Lopes, C. M., McNitt, S., Zareba, W., Goldenberg, I., Qi, M., Wilde, A. A. M., Shimizu, W., Kanters, Jørgen K., Towbin, J. A., Ackerman, M. J. & Robinson, J. L., 2009, In: Cardiovascular Electrophysiology. 20, 8, p. 859-865 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2
Christiansen, M., Hedley, P. L., Theilade, J., Stoevring, B., Leren, T. P., Eschen, O., Sørensen, K. M., Tybjærg-Hansen, Anne, Ousager, L. B., Pedersen, L. N., Frikke-Schmidt, Ruth, Aidt, F. H., Hansen, M. G., Hansen, J., Bloch Thomsen, P. E., Toft, E., Henriksen, F. L., Bundgård, Henning, Jensen, H. K. & Kanters, Jørgen K., 2014, In: BMC Medical Genetics. 15, 11 p., 31.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mutation Detection by Cleavase in Combination With Capillary Electrophoresis Analysis: Application to Mutations Causing Hypertrophic Cardiomyopathy and Long-QT Syndrome
Andersen, P. S., Larsen, L. A., Kanters, Jørgen K., Havndrup, O., Bundgaard, H., Brandt, N. J., Vuust, J. & Christiansen, M., 1998, In: Molecular Diagnosis and Therapy. Vol.3 No.2, p. 105-111Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Sterenborg, R. B. T. M., Steinbrenner, I., Li, Y., Bujnis, M. N., Naito, T., Marouli, E., Galesloot, T. E., Babajide, O., Andreasen, L., Astrup, A., Åsvold, B. O., Bandinelli, S., Beekman, M., Beilby, J. P., Bork-Jensen, J., Boutin, T., Brody, J. A., Brown, S. J., Brumpton, B., Campbell, P. J. & 121 others, , 2024, In: Nature Communications. 15, 1, 18 p., 888.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 9688
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Automatic J-point Location in Subjects with Electrocardiographic Early Repolarization
Research output: Contribution to journal › Journal article › Research › peer-review
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328
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Patients with Long QT Syndrome Due to Impaired hERG-encoded Kv11.1 Potassium Channel Have Exaggerated Endocrine Pancreatic and Incretin Function Associated with Reactive Hypoglycemia
Research output: Contribution to journal › Journal article › Research › peer-review
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264
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Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease
Research output: Contribution to journal › Journal article › Research › peer-review
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