Lars Hansen
Lars Hansen

senior adviser


  1. 2013
  2. Published

    Genetic heterogeneity in Pakistani microcephaly families

    Sajid Hussain, M., Bakhtiar, S. M., Farooq, Muhammad, Anjum, I., Janzen, E., Reza Toliat, M., Eiberg, Hans Rudolf Lytchoff, Kjær, Klaus Wilbrandt, Tommerup, Niels, Noegel, A. A., Nürnberg, P., Baig, S. M. & Hansen, Lars, May 2013, In : Clinical Genetics. 83, 5, p. 446-51 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability

    Hansen, Lars, Tawamie, H., Murakami, Y., Mang, Yuan, ur Rehman, S., Buchert, R., Schaffer, S., Muhammad, S., Bak, Mads, Nöthen, M. M., Bennett, Eric Paul, Maeda, Y., Aigner, M., Reis, A., Kinoshita, T., Tommerup, Niels, Baig, S. M. & Abou Jamra, R., 4 Apr 2013, In : American Journal of Human Genetics. 92, 4, p. 575-83 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinism

    Grønskov, K., Dooley, C. M., Østergaard, Elsebet, Kelsh, R. N., Hansen, Lars, Levesque, M. P., Vilhelmsen, K., Møllgård, Kjeld, Stemple, D. L. & Rosenberg, T., 7 Mar 2013, In : American Journal of Human Genetics. 92, 3, p. 415-21 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2012
  6. Published

    Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)

    Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Korbo, L., Nielsen, Inge-Merete, Svenstrup, K., Bech, S., Pinborg, L., Friberg, L., Hjermind, Lena Elisabeth, Olsen, O. & Nielsen, Jørgen Erik, Nov 2012, In : Clinical Genetics. 82, 3, p. 256-63 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Author response: Nonspecific PCR amplification of CRYBB2-pseudogene leads to misconception of natural variation as mutation

    Hansen, Lars & Rosenberg, T., 1 Sep 2012, In : Investigative Ophthalmology and Visual Science. 53, 10, 1 p.

    Research output: Contribution to journalLetterResearchpeer-review

  8. 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 articleResearchpeer-review

  9. 2011
  10. 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

  11. 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

  12. 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

  13. 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

ID: 544414