Lars Hansen

Lars Hansen

senior adviser


  1. 2008
  2. Published

    Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2

    Wissinger, B., Dangel, S., Jagle, H., Hansen, Lars, Baumann, B., Rudolph, G., Wolf, C., Bonin, M., Koeppen, K., Ladewig, T., Kohl, S., Zrenner, E. & Rosenberg, T., 2008, In : Investigative Ophthalmology & Visual Science. 49, 2, p. 751-757 6 p.

    Research output: Contribution to journalJournal article

  3. 2009
  4. Published

    Compound heterozygous ASPM mutations in Pakistani MCPH families

    Farooq, Muhammad, Mahmood Baig, S., Hansen, Lars, Sajid Hussain, M., Anjum Inayat, I., Aslam, M., Anver Qureshi, J., Toilat, M., Kirst, E., Wajid, M., Nürnberg, P., Eiberg, Hans Rudolf Lytchoff, Tommerup, Niels & Kjær, Klaus Wilbrandt, 2009, In : American Journal of Medical Genetics. Part A. 149A, 5, p. 926-30 4 p.

    Research output: Contribution to journalJournal article

  5. Published

    Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract

    Hansen, Lars, Mikkelsen, Annemette Friis, Nürnberg, P., Nürnberg, G., Anjum, I., Eiberg, Hans Rudolf Lytchoff & Rosenberg, T., 2009, In : Investigative Ophthalmology & Visual Science. 50, 7, p. 3291-303 12 p.

    Research output: Contribution to journalJournal article

  6. 2010
  7. Published

    A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family

    Anjum, I., Eiberg, Hans Rudolf Lytchoff, Baig, S. M., Tommerup, Niels & Hansen, Lars, Mar 2010, In : Molecular Vision. 16, p. 549-55 6 p.

    Research output: Contribution to journalJournal article

  8. Published

    Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS

    Farooq, Muhammad, Troelsen, J. T., Boyd, M., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hussain, M. S., Rehman, S. U., Azhar, A., Ali, A., Bakhtiar, S. M., Tommerup, Niels, Baig, S. M. & Kjær, Klaus Wilbrandt, Jun 2010, In : European Journal of Human Genetics. 18, 6, p. 733-6 3 p.

    Research output: Contribution to journalJournal article

  9. 2011
  10. 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 article

  11. 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 article

  12. 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 article

  13. 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 article

  14. 2012
  15. Published

    Genetic studies in congenital anterior midline cervical cleft

    Jakobsen, L. P., Pfeiffer, P., Andersen, M., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Mang, Yuan, Bak, Mads, Møller, R. S., Klitten, L. L. & Tommerup, Niels, Aug 2012, In : American Journal of Medical Genetics. Part A. 158A, 8, p. 2021-6 6 p.

    Research output: Contribution to journalJournal article

ID: 544414