Lisbeth Tranebjærg

Lisbeth Tranebjærg

Professor emeritus.

Member of:

  • Clinical Genetics


Publication year:
All
1 - 10 out of 113Page size: 10
  1. 1997
  2. Published

    Quantification, by solid-phase minisequencing, of the telomeric and centromeric copies of the survival motor neuron gene in families with spinal muscular atrophy

    Schwarz, M., Sørensen, N., Hansen, F. J., Hertz, J. M., Nørby, S., Tranebjærg, Lisbeth & Skovby, F., 1997, In: Human Molecular Genetics. 6, 1, p. 99-104

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

  3. 1998
  4. Published

    A neocentromere on human chromosome 3 without detectable alpha-satellite DNA forms morphologically normal kinetochores

    Wandall, A., Tranebjærg, Lisbeth & Tommerup, Niels, 1998, In: Chromosoma. 107, 6-7, p. 359-65 6 p.

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

  5. Published

    Apolipoprotein E alleles in mothers of trisomy 18 conceptuses

    Kreiner, Claus Thustrup, Bugge, Merete, Brandt, C. A., Hertz, J. M., Tranebjærg, Lisbeth, Mikkelsen, M. & Petersen, M. B., 1998, In: Clinical Genetics. 53, 4, p. 321-322

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

  6. Published

    Machado-Joseph disease in three Scandinavian families

    Løkkegaard, T., Nielsen, J. E., Hasholt, Lis Frydenreich, Fenger, K., Werdelin, L., Tranebjærg, Lisbeth, Lauritzen, Martin, Colding-Jørgensen, E., Grønbech-Jensen, M., Henriksen, O. A. & Sørensen, S. A., 1998, In: Journal of Neurological Sciences. 156, 2, p. 152-157

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

  7. Published

    Non-disjunction of chromosome 18

    Bugge, Merete, Collins, A., Petersen, M. B., Fisher, J., Brandt, C. A., Hertz, J. M., Tranebjærg, Lisbeth, de Lozier-Blanchet, C., Nicolaides, P., Brøndum-Nielsen, K., Morton, N. & Mikkelsen, M., 1998, In: Human Molecular Genetics. 7, 4, p. 661-669

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

  8. 2000
  9. Published

    Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia

    Lund, A., Udd, B., Juvonen, V., Andersen, P. M., Cederquist, K., Ronnevi, L., Sistonen, P., Sørensen, S. A., Tranebjærg, Lisbeth, Wallgren-Pettersson, C. & Savontaus, M., 2000, In: European Journal of Human Genetics. 8, 8, p. 631-636

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

  10. 2001
  11. Published

    Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world

    Lund, A., Udd, B., Juvonen, V., Andersen, P. M., Cederquist, K., Davis, M., Cellera, C., Kölmel, C., Ronnevi, L., Sperfeld, A., Sørensen, S. A., Tranebjærg, Lisbeth, Van Maldergem, L., Watanabe, M., Weber, M. J., Yeung, L. & Savontaus, M., 2001, In: European Journal of Human Genetics. 9, 6, p. 431-436

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

  12. 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

  13. Published

    Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study

    Gaspar, C., Lopes-Cendes, I., Hayes, S., Goto, J., Arvidsson, K., Dias, A., Silveira, I., Maciel, P., Coutinho, P., Lima, M., Zhou, Y. X., Soong, B. W., Watanabe, M., Giunti, P., Stevanin, G., Riess, O., Sasaki, H., Hsieh, M., Nicholson, G. A., Brunt, E. & 10 others, Higgins, J. J., Lauritzen, Martin, Tranebjærg, Lisbeth, Volpini, V., Wood, N., Ranum, L., Tsuji, S., Brice, A., Sequeiros, J. & Rouleau, G. A., 1 Jan 2001, In: American Journal of Human Genetics. 68, 2, p. 523-528 6 p.

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

  14. 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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ID: 1571395