Lars Hansen

Lars Hansen

Guest researcher


  1. 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

  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

    A validated collection of mouse monoclonal antibodies to human glycosyltransferases functioning in mucin-type O-glycosylation.

    Steentoft, Catharina, Yang, Z., Wang, S., Ju, T., Vester-Christensen, M. B., Festari, M. F., King-Smith, S. L., Moremen, K., Larsen, Ida Signe Bohse, Goth, Christoffer Knak, Schjoldager, Katrine Ter-Borch Gram, Hansen, Lars, Bennett, Eric Paul, Mandel, Ulla & Narimatsu, Y., 2019, In: Glycobiology. 29, 9, p. 645–656 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells

    Tian, W., Ye, Zilu, Wang, S., Schulz, M. A., Van Coillie, Julie, Sun, L., Chen, Y., Narimatsu, Y., Hansen, Lars, Kristensen, C., Mandel, Ulla, Bennett, Eric Paul, Jabbarzadeh-Tabrizi, S., Schiffmann, R., Shen, J., Vakhrushev, Sergey, Clausen, Henrik & Yang, Z., 2019, In: Nature Communications. 10, 13 p., 1785.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

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

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

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

  6. Published

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

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

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

  7. Published

    Site-specific O-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactions

    Wang, S., Mao, Y., Narimatsu, Y., Ye, Zilu, Tian, W., Goth, Christoffer Knak, Lira-Navarrete, E., Pedersen, N. B., Benito-Vicente, A., Martin, C., Uribe, K. B., Hurtado-Guerrero, R., Christoffersen, Christina, Seidah, N. G., Nielsen, R., Christensen, E. I., Hansen, Lars, Bennett, Eric Paul, Vakhrushev, Sergey, Schjoldager, Katrine Ter-Borch Gram & Clausen, Henrik, 2018, In: The Journal of Biological Chemistry. 293, 19, p. 7408 –7422

    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

    Fast and sensitive detection of indels induced by precise gene targeting

    Yang, Z., 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, 2015, In: Nucleic Acids Research. 43, 9, p. 1-8 8 p., e59.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function

    Zilmer, M., Edmondson, A. C., Khetarpal, S. A., Alesi, V., Zaki, M. S., Rostasy, K., Madsen, C. G., Lepri, F. R., Sinibaldi, L., Cusmai, R., Novelli, A., Issa, M. Y., Fenger, C. D., Jamra, R. A., Reutter, H., Briuglia, S., Agolini, E., Hansen, Lars, Petäjä-Repo, U. E., Hintze, John, Raymond, K. M., Liedtke, K., Stanley, V., Musaev, D., Gleeson, J. G., Vitali, C., O’Brien, W. T., Gardella, E., Rubboli, Guido, Rader, D. J., Schjoldager, Katrine Ter-Borch Gram & Møller, R. S., 2020, In: Brain. 143, 4, p. 1114-1126 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 544414