Lars Allan Larsen

Lars Allan Larsen

Professor


  1. 2007
  2. Published

    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 journalJournal articleResearchpeer-review

  3. Published

    Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2

    Jakobsen, L. P., Ullmann, R., Christensen, S. B., Jensen, K. E., Molsted, K., Henriksen, K. F., Hansen, C., Knudsen, M. A. F., Larsen, Lars Allan, Tommerup, Niels & Tümer, Asuman Zeynep, 2007, In: Journal of Medical Genetics. 44, 6, p. 381-386 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Single-strand conformation polymorphism analysis using capillary array electrophoresis for large-scale mutation detection

    Larsen, Lars Allan, Jespersgaard, C. & Andersen, P. S., 2007, In: Nature Protocols (Print Edition). 2, 6, p. 1458-1466 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    YKL-40 protein expression in the early developing human musculoskeletal system

    Johansen, J. S., Høyer, P. E., Larsen, Lars Allan, Price, P. A. & Møllgård, Kjeld, 2007, In: Journal of Histochemistry & Cytochemistry. 55, 12, p. 1213-1228 15 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 2006
  7. Published

    Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease

    Baekvad-Hansen, M., Tümer, Asuman Zeynep, Delicado, A., Erdogan, F., Tommerup, Niels & Larsen, Lars Allan, 2006, In: American Journal of Medical Genetics. Part A. 140A, 5, p. 427-433 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Evaluation of two methods for generating cRNA for microarray experiments from nanogram amounts of total RNA.

    Bak, M., Conley, L., Hedegaard, J., Larsen, Lars Allan, Sørensen, P., Bendixen, C. & Tommerup, Niels, 2006, In: Analytical Biochemistry. 358, 1, p. 111-9 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Hedgehog signaling in small-cell lung cancer: Frequent in vivo but a rare event in vitro

    Vestergaard, J., Pedersen, M. W., Pedersen, N., Ensinger, C., Tümer, Asuman Zeynep, Tommerup, Niels, Poulsen, H. S. & Larsen, Lars Allan, 2006, In: Lung Cancer. 52, 3, p. 281-290 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Optimization of capillary array electrophoresis single-strand conformation polymorphism analysis for routine molecular diagnostics

    Jespersgaard, C., Larsen, Lars Allan, Baba, S., Kukita, Y., Tahira, T., Christiansen, M., Vuust, J., Hayashi, K. & Andersen, P. S., 2006, In: Electrophoresis. 27, 19, p. 3816-3822 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Screening for fragilt X-syndrom. Internationale erfaringer

    Vuust, J., Larsen, Lars Allan, Gronskov, K., Norgaard-Pedersen, B. & Brondum-Nielsen, K., 2006, In: Ugeskrift for læger. 168, 43, p. 3704-3709 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Screening of 99 Danish patients with congenital heart disease for GATA4 mutations

    Zhang, L., Tümer, Asuman Zeynep, Jacobsen, J. R., Andersen, P. S., Tommerup, Niels & Larsen, Lars Allan, 2006, In: Genetic Testing. 10, 4, p. 277-80 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. 2005
  14. Published

    Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

    Boonen, S. E., Stahl, D., Kreiborg, S., Rosenberg, T., Kalscheuer, V., Larsen, Lars Allan, Tommerup, Niels & Brøndum-Nielsen, K., 2005, In: American Journal of Medical Genetics. Part A. Vol. 132, p. 324-328

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    High Throughput Single-Strand Conformation Polymorphism Analysis on a Microfabricated Capillary Array Electrophoresis Dervice

    Tian, H., Emrich, C. A., Scherer, J., Mathies, R. A., Andersen, P. S., Larsen, Lars Allan & Christiansen, M., 2005, In: Electrophoresis. Vol. 26, p. 1834-1842

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. Published

    Mutations in the HERG ion channel: A novel link between long QT syndrome and sudden death syndrome

    Christiansen, M., Tønder, N., Larsen, Lars Allan, Andersen, P. S., Simonsen, H. B., Øyen, N., Kanters, J. K., Jacobsen, J. R., Fosdal, I., Wettrell, G. & Kjeldsen, K., 2005, In: American Journal of Cardiology. Vol. 95, p. 433-434

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

    Mutations in the genes KCND2 and KCND3 encoding the ion-channels Kv 4.2. and Kv 4.3, conducting the cardiac fast transient outward current ( ITo,f), are not a frequent cause of Long QT syndrome

    Frank-Hansen, R., Larsen, Lars Allan, Andersen, P. S., Jespersgård, C. & Christiansen, M., 2005, In: Clinica Chimica Acta. Vol. 351, p. 95-100

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region

    Hougs, L., Havndrup, O., Bundgård, Henning, Køber, Lars Valeur, Vuust, J., Larsen, Lars Allan, Christiansen, M. & Andersen, P. S., 2005, In: European Journal of Human Genetics. 13, 2, p. 161-5 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    One-third of Danish hyperytrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region

    Hougs, L., Havndrup, O., Bundgaard, H., Køber, L., Vuust, J., Larsen, Lars Allan, Christiansen, M. & Andersen, P. S., 2005, In: European Journal of Human Genetics. Vol. 13, p. 161-165

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. Published

    Potassium Must Be Considered in Congenital Long QT Syndrome

    Christiansen, M., Kjeldsen, K., Wettrell, G., Larsen, Lars Allan, Lundkvist, L., Andersen, P. S., Tran, C. T., Kanters, J. K. & Vuust, J., 2005, In: Cardiology. Vol. 5, p. 54-58

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. Published

    The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome

    Tümer, Asuman Zeynep, Henriksen, A. M., Bache, Iben, Larsen, Lars Allan, Brixen, K., Illum, N., Rasmussen, K. & Tommerup, Niels, 2005, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 135A, p. 339-341

    Research output: Contribution to journalJournal articleResearchpeer-review

  22. 2004
  23. Published

    Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

    Boonen, S. E., Stahl, D., Kreiborg, Sven, Rosenberg, T., Kalscheuer, V., Larsen, Lars Allan, Tommerup, Niels, Brøndum-Nielsen, K. & Tümer, Asuman Zeynep, 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 132A, p. 324-328

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    Does KCNE5 play a role in long QT syndrome?

    Hofman-Bang, J., Jespersen, Thomas, Grunnet, Morten, Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Kjeldsen, K. & Christiansen, M., 2004, In: Clinica Chimica Acta. 345, 1-2, p. 49-53 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairment

    Grønskov, K., Larsen, Lars Allan, Rendtorff, N. D., Parving, A., Nørgaard-Pedersen, B. & Brøndum-Nielsen, K., 2004, In: Genet Test. Vol. 8, p. 181-184

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. Published

    Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

    Andersen, P. S., Havndrup, O., Bundgaard, H., Larsen, Lars Allan, Vuust, J., Pedersen, A. K., Kjeldsen, K. & Christiansen, M., 2004, In: European Journal of Human Genetics. Vol. 12, p. 673-677

    Research output: Contribution to journalJournal articleResearchpeer-review

  27. Published

    High Throughput Mutation Screening

    Andersen, P. S. & Larsen, Lars Allan, 2004, Molecular Analysis and Genome Discovery. New York: IEEE Computer Society Press, p. chap. 5

    Research output: Chapter in Book/Report/Conference proceedingReport chapterResearch

  28. Published

    Identification of a novel EYA1 splice-site mutation in a Danish branchio-oto-renal syndrome family

    Henriksen, A. M., Tümer, Asuman Zeynep, Tommerup, Niels, Tranebjærg, Lisbeth & Larsen, Lars Allan, 2004, In: Genetic Testing. 8, 4, p. 404-6 2 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  29. Published

    T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome

    Kanters, J. K., Fanoe, S., Larsen, Lars Allan, Bloch-Thomsen, P. E., Toft, E. & Christansen, M., 2004, In: Heart Rhythm. Vol. 1, p. 285-292

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 2949