Lars Allan Larsen

Lars Allan Larsen

Professor

Member of:


    Publication year:
    All
    1 - 10 out of 83Page size: 10
    1. 1997
    2. Published

      High-throughput analysis of Fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis

      Larsen, Lars Allan, Grønskov, K., Nørgaard-Pedersen, B., Brøndum-Nielsen, K., Hasholt, Lis Frydenreich & Vuunst, J., 1997, In: Human Genetics. 100, p. 564-568

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

    3. 1998
    4. Published

      Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome

      Kanters, Jørgen K., Larsen, Lars Allan, Orholm, M., Agner, E., Andersen, P. S., Vuust, J. & Christiansen, M., 1 Jan 1998, In: Journal of Cardiovascular Electrophysiology. 9, 6, p. 620-624 5 p.

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

    5. 2001
    6. 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

    7. Published

      Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome

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

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

    8. 2003
    9. 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

    10. 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

    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. 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

    13. 2004
    14. 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

    15. 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

    Previous 1 2 3 4 5 6 7 8 9 Next

    ID: 2949