Nicole Schmitt

Nicole Schmitt

Professor with special responsibilities


  1. 2018
  2. Published

    Multiple genetic variations in sodium channel subunits in a case of sudden infant death syndrome

    Denti, F., Bentzen, Bo Hjorth, Wojciak, J., Thomsen, N. M., Scheinman, M. & Schmitt, Nicole, 2018, In : Pacing and Clinical Electrophysiology. 41, 6, p. 620-626

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    PKD Phosphorylation as Novel Pathway of KV11.1 Regulation

    Steffensen, Annette Buur, Bomholtz, S. H., Andersen, M. N., Olsen, Jesper Velgaard, Mutsaers, N., Lundegaard, Pia Rengtved, Lundby, Alicia & Schmitt, Nicole, 2018, In : Cellular Physiology and Biochemistry. 47, 4, p. 1742-1750 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Spinal dorsal horn astrocytes release GABA in response to synaptic activation

    Christensen, R. K., Delgado-Lezama, R., Russo, R. E., Lind, Barbara Lykke, Alcocer, E. L., Rath, Martin Fredensborg, Fabbiani, G., Schmitt, Nicole, Lauritzen, Martin, Petersen, A. V., Carlsen, Eva Maria Meier & Perrier, Jean-Francois Marie, 2018, In : The Journal of Physiology. 596, 20, p. 4983-4994 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation

    Denti, F., Paludan-Müller, C., Olesen, Søren-Peter, Haunsø, Stig, Svendsen, Jesper Hastrup, Olesen, Morten Steen Salling, Bentzen, Bo Hjorth & Schmitt, Nicole, Mar 2018, In : Personalized Medicine. 15, 2, p. 93-102 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    SUMO co-expression modifies KV 11.1 channel activity

    Steffensen, Annette Buur, Andersen, M. N., Mutsaers, N., Mujezinovic, A. & Schmitt, Nicole, Mar 2018, In : Acta Physiologica (Print). 222, 3, 11 p., e12974.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. 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

ID: 5624