Lars Allan Larsen

Lars Allan Larsen

Professor

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    Publication year:
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    71 - 80 out of 83Page size: 10
    1. 2004
    2. 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

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

    4. 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 proceeding › Report chapter › Research

    5. 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

    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

      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

    11. 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

    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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