Lars Hansen

Lars Hansen

Guest researcher


  1. 2005
  2. Published

    A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions

    Kjær, Klaus Wilbrandt, Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Utkus, A., Skovgaard, Lene Theil, Leicht, P., Opitz, J. M. & Tommerup, Niels, 2005, In : American Journal of Medical Genetics. Part A. 138, 4, p. 328-39 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG

    Kjær, Klaus Wilbrandt, Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Christensen, K. S., Opitz, J. M. & Tommerup, Niels, 2005, In : American Journal of Medical Genetics. Part A. 137, 2, p. 148-52 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified

    Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Barrett, T., Bek, T., Kjærsgaard, P., Tranebjærg, Lisbeth & Rosenberg, T., 2005, In : European Journal of Human Genetics. 13, 12, p. 1275-1284

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1

    Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hansen, C., Mohr, J., Teglbjærg, P. S. & Kjær, Klaus Wilbrandt, 15 Feb 2005, In : American Journal of Medical Genetics. 133 A, 1, p. 44-47 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 2006
  7. Published

    A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2

    Kjær, Klaus Wilbrandt, Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hagen, C. B. V. D., Rosendahl, K., Tommerup, Niels & Mundlos, S., 2006, In : Journal of Medical Genetics. 43, 3, p. 225-231 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

    Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Kjer, B., Hansen, T., Pedersen, O., Bille, M., Rosenberg, T. & Tranebjaerg, L., 2006, In : Journal of Medical Genetics. 43, 5, p. 435-440 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46

    Hansen, Lars, Yao, W., Eiberg, Hans Rudolf Lytchoff, Funding, M., Riise, R., Kjær, Klaus Wilbrandt, Hejtmancik, J. F. & Rosenberg, T., 2006, In : Molecular Vision. 12, 116, p. 1033-1039 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. 2007
  11. Published

    Genetic heterogeneity in microcornea-cataract: Five novel mutations in CRYAA, CRYGD, and GJA

    Hansen, Lars, Yao, W. L., Eiberg, Hans Rudolf Lytchoff, Kjær, Klaus Wilbrandt, Baggesen, K., Hejtmancik, J. F. & Rosenberg, T., 2007, In : Investigative Ophthalmology & Visual Science. 48, 9, p. 3937-3944 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. 2008
  13. Published

    A novel mutation in IRF6 resulting in VWS-PPS spectrum disorder with renal aplasia

    Medeiros, F. D., Hansen, Lars, Mawlad, E., Eiberg, Hans Rudolf Lytchoff, Asklund, C., Tommerup, Niels & Jakobsen, L. P., 2008, In : American Journal of Medical Genetics. Part A. 146A, 12, p. 1605-1608 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.

    Eiberg, Hans Rudolf Lytchoff, Troelsen, J., Boyd, M., Mikkelsen, Annemette Friis, Mengel-From, J., Kjær, Klaus Wilbrandt & Hansen, Lars, 2008, In : Human Genetics. 123, 2, p. 177-87 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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