Christian Paludan-Müller

Christian Paludan-Müller

Guest researcher


Publication year:
All
1 - 10 out of 10Page size: 10
  1. 2023
  2. Published

    CineECG analysis provides new insights into Familial ST-segment Depression Syndrome

    Frosted, R., Paludan-Müller, Christian, Vad, Oliver Tim Bundgaard, Olesen, Morten Steen Salling, Bundgård, Henning, van Dam, P. & Christensen, Alex Hørby, 2023, In: Europace. 25, 5, 11 p., euad116.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    Genetically predicted adipose tissue distribution influences the risk of atherosclerosis

    Vad, Oliver Tim Bundgaard, Paludan-Müller, Christian, Monfort, L. M., Ahlberg, Gustav, Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2023, In: European Journal of Preventive Cardiology. 30, 7, p. e41–e45

    Research output: Contribution to journal › Letter › Research › peer-review

  4. 2022
  5. Published

    Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population.

    Paludan-Müller, Christian, Larsen, S., Ahlberg, G., Monfort, L. M., Andreasen, L., Svendsen, Jesper Hastrup, Jespersen, Thomas, Bundgård, Henning, Kanters, Jørgen K. & Olesen, Morten Steen Salling, 2022, In: Circulation. Genomic and precision medicine. 15, 1, p. 83-85 3 p., e003574.

    Research output: Contribution to journal › Letter › Research › peer-review

  6. Published

    Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT

    Andreasen, L., Ahlberg, G., Ægisdóttir, H. M., Sveinbjörnsson, G., Lundegaard, Pia Rengtved, Hartmann, J. P., Paludan-Müller, Christian, Hadji-Turdeghal, Katra, Ghouse, Jonas, Pehrson, S., Jensen, H. K., Riahi, S., Hansen, J., Sandgaard, N., Sørensen, E., Banasik, Karina, Sækmose, S. G., Bruun, M. T., Hjalgrim, Henrik, Erikstrup, C., Pedersen, Ole Birger Vesterager, Wittig, M., Haunsø, Stig, Ostrowski, Sisse Rye, Genomic Consortium, D., Franke, A., Brunak, Søren, Kanters, Jørgen K., Ellervik, Christina, Bundgård, Henning, Ullum, H., Gudbjartsson, D. F., Thorsteinsdottir, U., Holm, H., Arnar, D. O., Stefansson, K., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2022, In: Circulation Research. 131, 10, p. 862-865

    Research output: Contribution to journal › Letter › Research › peer-review

  7. 2020
  8. Published

    Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation

    Vad, O. B., Paludan-Müller, Christian, Ahlberg, G., Kalsto, S. M., Ghouse, Jonas, Andreasen, Laura Korsholm, Haunsø, Stig, Tveit, A., Sajadieh, Ahmad, Christophersen, I. E., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2020, In: Journal of Clinical Medicine. 9, 2, 12 p., 372.

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. 2019
  10. 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 journal › Journal article › Research › peer-review

  11. 2018
  12. Published

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

    Denti, F., Paludan-Müller, Christian, 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 journal › Journal article › Research › peer-review

  13. 2017
  14. Published

    Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants

    Paludan-Müller, Christian, Ahlberg, Gustav, Ghouse, Jonas, Herfelt, C., Svendsen, Jesper Hastrup, Haunsø, Stig, Kanters, Jørgen K. & Olesen, Morten Steen Salling, Jan 2017, In: Clinical Genetics. 91, 1, p. 63–72

    Research output: Contribution to journal › Journal article › Research › peer-review

  15. Published

    Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease

    Paludan-Müller, Christian, Ahlberg, G., Ghouse, Jonas, Svendsen, Jesper Hastrup, Haunsø, Stig & Olesen, Morten Steen Salling, 2017, In: Circulation. Cardiovascular genetics. 10, 6, 10 p., e001878.

    Research output: Contribution to journal › Journal article › Research › peer-review

  16. 2016
  17. Published

    The role of common genetic variants in atrial fibrillation

    Paludan-Müller, Christian, Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2016, In: Journal of Electrocardiology. 49, 6, p. 864-870

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 256925332