Nicole Schmitt

Nicole Schmitt

Professor with special responsibilities


  1. 2022
  2. Published

    A benzodiazepine activator locks Kv7.1 channels open by electro-mechanical uncoupling

    Schreiber, J. A., Möller, M., Zaydman, M., Zhao, L., Beller, Z., Becker, S., Ritter, N., Hou, P., Shi, J., Silva, J., Wrobel, E., Strutz-Seebohm, N., Decher, N., Schmitt, Nicole, Meuth, S. G., Düfer, M., Wünsch, B., Cui, J. & Seebohm, G., 2022, In: Communications Biology . 5, 1, p. 1-13 301.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation

    Vad, Oliver Tim Bundgaard, Yan, Yannan, Denti, F., Ahlberg, Gustav, Refsgaard, L., Bomholtz, Sofia Hammami, Louro Larupa dos Santos, Joana, Rasmussen, Simon, Haunsø, Stig, Svendsen, Jesper Hastrup, Christophersen, I. E., Schmitt, Nicole, Olesen, Morten Steen Salling & Bentzen, Bo Hjorth, 2022, In: Frontiers in Genetics. 13, 8 p., 806429.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. 2021
  5. Published

    The Tunicate Metabolite 2-(3,5-Diiodo-4-methoxyphenyl)ethan-1-amine Targets Ion Channels of Vertebrate Sensory Neurons

    Paguigan, N. D., Yan, Yannan, Karthikeyan, M., Chase, K., Carter, J., Leavitt, L. S., Lim, A. L., Lin, Z., Memon, T., Christensen, S., Bentzen, Bo Hjorth, Schmitt, Nicole, Reilly, C. A., Teichert, R. W., Raghuraman, S., Olivera, B. M. & Schmidt, E. W., 2021, In: ACS chemical biology. 16, 9, p. 1654-1662

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 2020
  7. Published

    A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation

    Hansen, T. H., Yan, Yannan, Ahlberg, G., Vad, O. B., Refsgaard, L., Louro Larupa dos Santos, Joana, Mutsaers, N., Svendsen, Jesper Hastrup, Olesen, Morten Steen Salling, Bentzen, Bo Hjorth & Schmitt, Nicole, 29 Jan 2020, In: Scientific Reports. 10, 1, 10 p., 1453.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Functional phenotype variations of two novel Kv 7.1 mutations identified in patients with Long QT syndrome

    Bomholtz, Sofia Hammami, Refaat, M., Steffensen, Annette Buur, David, J., Espinosa, K., Nussbaum, R., Wojciak, J., Bentzen, Bo Hjorth, Scheinman, M. & Schmitt, Nicole, 2020, In: Pacing and Clinical Electrophysiology. 43, 2, p. 210-216 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published
  10. Published

    Treatments for paroxysmal supraventricular tachycardia: A review of current practice

    Rajan, D. & Schmitt, Nicole, 2020, In: World Heart Journal. 12, 3, p. 257-268

    Research output: Contribution to journalReviewResearchpeer-review

  11. 2019
  12. Published

    Deletion in mice of X-linked, Brugada syndrome- and atrial fibrillation-associated Kcne5 augments ventricular KV currents and predisposes to ventricular arrhythmia

    David, J., Lisewski, U., Crump, S. M., Jepps, Thomas Andrew Qvistgaard, Bocksteins, E., Wilck, N., Lossie, J., Roepke, T. K., Schmitt, Nicole & Abbott, G. W., Feb 2019, In: FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 33, 2, p. 2537-2552 16 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts

    Paludan-Müller, Christian, Ghouse, Jonas, Vad, O. B., Herfelt, C. B., Lundegaard, Pia Rengtved, Ahlberg, G., Schmitt, Nicole, Svendsen, Jesper Hastrup, Haunsø, Stig, Bundgård, Henning, Hansen, Torben, Kanters, Jørgen K. & Olesen, Morten Steen Salling, 2019, In: European Journal of Human Genetics. 27, 9, p. 1427-1435

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. 2018
  15. Published

    Homozygosity for SCN4A Arg1142Gln causes congenital myopathy with variable disease expression

    Sloth, C. K., Denti, F., Schmitt, Nicole, Bentzen, Bo Hjorth, Fagerberg, C., Vissing, John & Gaist, D., Oct 2018, In: Neurology: Genetics. 4, 5, p. e267 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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