Lars Hansen

Lars Hansen

senior adviser


  1. Published

    An Atlas of Human Glycosylation Pathways Enables Display of the Human Glycome by Gene Engineered Cells

    Narimatsu, Yoshiki, Joshi, Hiren Jitendra, pxs190, pxs190, Van Coillie, Julie, Karlsson, R., Sun, L., Ye, Zilu, Chen, Y., Schjoldager, Katrine Ter-Borch Gram, Steentoft, Catharina, Furukawa, S., Bensing, B. A., Sullam, P. M., Thompson, A. J., Paulson, J. C., Büll, Christian, Adema, G. J., Mandel, Ulla, Hansen, Lars, Bennett, Eric Paul, Varki, A., Vakhrushev, Sergey, Yang, Zhang & Clausen, Henrik, 2019, In : Molecular Cell. 75, 2, p. 394-407, e1-e5

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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 articleResearchpeer-review

  7. 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 articleResearchpeer-review

  8. 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 articleResearchpeer-review

  9. Published
  10. Published

    Fast and sensitive detection of indels induced by precise gene targeting

    Yang, Zhang, Steentoft, Catharina, Hauge, C., Hansen, Lars, Thomsen, A. L., Niola, Francesco, Vester-Christensen, M. B., Frödin, Morten, Clausen, Henrik, Wandall, Hans H. & Bennett, Eric Paul, 19 May 2015, In : Nucleic Acids Research. 43, 9, p. 1-8 8 p., e59.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 544414