Jørgen K. Kanters
Associate Professor
Physiology of circulation, kidney and lung
Blegdamsvej 3
2200 København N.
- 2001
- Published
Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome
Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Svendsen, I. H., Jacobsen, J. R., Vuust, J., Wetrell, G., Tranebjærg, Lisbeth & Christiansen, M., 2001, In: Clinical Chemistry. 47, 8, p. 1390-1395Research output: Contribution to journal › Journal article › Research › peer-review
- 2000
- Published
Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2
Larsen, L. A., Svendsen, I. H., Jensen, A. M., Kanters, Jørgen K., Andersen, P. S., Møller, M., Sørensen, S. A., Sandøe, E., Jacobsen, J. R., Vuust, J. & Christiansen, M., 2000, In: Clinical Genetics. 57, p. 125-130Research output: Contribution to journal › Journal article › Research › peer-review
- 1999
- Published
A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome
Larsen, L. A., Andersen, P. S., Kanters, Jørgen K., Jabobsen, J. R., Vuust, J. & Christensen, M., 1999, In: Clinica Chimica Acta. 280, p. 113-125Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Approximate entropy and point correlation dimension of heart rate variability in healthy subjects.
Storella, R. J., Wood, H. W., Mills, K. M., Kanters, Jørgen K., Højgaard, M. V. & von Holstein-Rathlou, Niels-Henrik, 1999, In: Integrative Physiological & Behavioral Science. 33, 4, p. 315-20 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Calciumantagonister
Agner, E. & Kanters, Jørgen K., 1999, In: Maanedsskrift for Praktisk Laegegerning. 77, p. 325-335Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Recessive romano-ward syndrome associated with compound heterozygosity for two mutations in the KvLQT1 gene
Larsen, L. A., Forsdal, I., Andersen, P. S., Kanters, Jørgen K., Vuust, J., Wetrell, G. & Christiansen, M., 1999, In: European Journal of Human Genetics. 7, p. 724-728Research output: Contribution to journal › Journal article › Research › peer-review
- 1998
- Published
Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome
Kanters, Jørgen K., Larsen, Lars Allan, Orholm, M., Agner, E., Andersen, P. S., Vuust, J. & Christiansen, M., 1 Jan 1998, In: Journal of Cardiovascular Electrophysiology. 9, 6, p. 620-624 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Dynamics of spectral components of heart rate variability during changes in autonomic balance.
Højgaard, M. V., von Holstein-Rathlou, Niels-Henrik, Agner, E. & Kanters, Jørgen K., 1998, In: American Journal of Physiology (Consolidated). 275, 1 Pt 2, p. H213-9Research 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
Novel donor splice site mutation in the KvLQT1 gene is associated Long QT syndrome
Kanters, Jørgen K., Larsen, L. A., Orholm, M., Agner, E., Andersen, P. S., Vuust, J. & Christiansen, M., 1998, In: Cardiovascular Electrophysiology. 9, p. 620-624Research output: Contribution to journal › Journal article › Research › peer-review
ID: 9688
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983
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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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333
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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
Published -
266
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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
Published