Lars Hansen

Lars Hansen

senior adviser


  1. Published

    RUNX2 analysis of Danish cleidocranial dysplasia families

    Hansen, Lars, Riis, A. K., Silahtaroglu, Asli, Hove, H., Lauridsen, Erling, Eiberg, Hans Rudolf Lytchoff & Kreiborg, Sven, 2011, In : Clinical Genetics. 79, 3, p. 254-63 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Published

    500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip

    Jakobsen, L. P., Bugge, Merete, Ullmann, R., Schjerling, C. K., Borup, R., Hansen, Lars, Eiberg, Hans Rudolf Lytchoff & Tommerup, Niels, 1 Mar 2011, In : American Journal of Medical Genetics. Part A. 155, 3, p. 652-5 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

    Rehman, S. U., Baig, S. M., Eiberg, Hans Rudolf Lytchoff, Rehman, S. U., Ahmad, I., Malik, N. A., Tommerup, Niels & Hansen, Lars, 2011, In : Neurogenetics. 12, 3, p. 247-51 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

    Rendtorff, N. D., Lodahl, M., Boulahbel, H., Johansen, I. R., Pandya, A., Welch, K. O., Norris, V. W., Arnos, K. S., Bitner-Glindzicz, M., Emery, S. B., Mets, M. B., Fagerheim, T., Eriksson, K., Hansen, Lars, Bruhn, H., Möller, C., Lindholm, S., Ensgaard, S., Lesperance, M. M. & Tranebjærg, Lisbeth, 2011, In : American Journal of Medical Genetics. Part A. 155, 6, p. 1298-313 16 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 544414