Lars Allan Larsen

Lars Allan Larsen

Professor

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    71 - 80 out of 83Page size: 10
    1. 2004
    2. 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 journal › Journal article › Research › peer-review

    3. 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 journal › Journal article › Research › peer-review

    4. 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 journal › Journal article › Research › peer-review

    5. 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 journal › Journal article › Research › peer-review

    6. 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 journal › Journal article › Research › peer-review

    7. 2003
    8. Published

      Capillary electrophoresis-based single stand dna conformation analysis in high-throughput mutation screening

      Andersen, P. S., Jespersgaard, C., Vuust, J., Christiansen, M. & Larsen, Lars Allan, 2003, In: Human Mutation. Vol. 21, p. 455-65

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

    9. Published

      High-througput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method

      Andersen, P. S., Jespersgaard, C., Vuust, J., Christiansen, M. & Larsen, Lars Allan, 2003, In: Human Mutation. Vol. 21, p. 116-122

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

    10. Published

      The Hedgehog signaling pathway - implications for drug targets in cancer and neurodegenerative disorders

      Bak, M., Hansen, C., Tommerup, Niels & Larsen, Lars Allan, 2003, In: Pharmacogenomics. Vol. 4, p. 411-429

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

    11. Published

      Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations

      Havndrup, O., Bundgaard, H., Andersen, P. S., Larsen, Lars Allan, Vuust, J., Kjeldsen, K. & Christiansen, M., 2003, In: Cardiovascular Research. Vol. 57, p. 298-301

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

    12. 2001
    13. Published

      Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome

      Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Svendsen, I. H., Jacobsen, J. R., Vuust, J., Wettrell, G., Tranebjærg, Lisbeth, Bathen, J. & Christiansen, M., 6 Aug 2001, In: Clinical Chemistry. 47, 8, p. 1390-1395 6 p.

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

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