Lars Hansen

Lars Hansen

Guest researcher


  1. 2014
  2. Published

    The myosin chaperone UNC45B is involved in lens development and autosomal dominant juvenile cataract

    Hansen, Lars, Comyn, S., Mang, Yuan, Lind-Thomsen, A., Myhre, L., Jean, F., Eiberg, Hans Rudolf Lytchoff, Tommerup, Niels, Rosenberg, T. & Pilgrim, D., Nov 2014, In : European Journal of Human Genetics. 22, 11, p. 1290-1297 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Immature truncated O-glycophenotype of cancer directly induces oncogenic features

    Radhakrishnan, P., Dabelsteen, Sally, Madsen, F. B., Francavilla, C., Kopp, K. L., Steentoft, Catharina, Vakhrushev, Sergey, Olsen, Jesper Velgaard, Hansen, Lars, Bennett, Eric Paul, Woetmann, A., Yin, G., Chen, L., Song, H., Bak, Mads, Hlady, R. A., Peters, S. L., Opavsky, R., Thode, C., Qvortrup, Klaus, Schjoldager, Katrine Ter-Borch Gram, Clausen, Henrik, Hollingsworth, M. A. & Wandall, Hans H., 12 Aug 2014, In : Proceedings of the National Academy of Sciences of the United States of America. 111, 39, p. e4066-e4077 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    UDP-gal: BetaGlcNAc Beta 1,3-galactosyltransferase, polypeptide 1,2 (B3GALT1,2)

    Vester-Christensen, M. B., Hansen, Lars & Clausen, Henrik, 1 Jan 2014, Handbook of Glycosyltransferases and Related Genes, Second Edition. Springer Japan, Vol. 1. p. 73-80 8 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

  5. Published

    UDP-gal: BetaGal beta 1,3-galactosyltransferase polypeptide 6 (B3GALT6)

    Vester-Christensen, M. B., Hansen, Lars & Clausen, Henrik, 1 Jan 2014, Handbook of Glycosyltransferases and Related Genes, Second Edition. Springer Japan, Vol. 1. p. 101-108 8 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

  6. 2013
  7. 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

  8. 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

  9. 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

  10. 2012
  11. 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, L., Olsen, O. & Nielsen, Jørgen Erik, Nov 2012, In : Clinical Genetics. 82, 3, p. 256-63 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. 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

  13. Published

    Genetic studies in congenital anterior midline cervical cleft

    Jakobsen, Linda Plovmand, 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

ID: 544414