Lars Hansen

Lars Hansen

Guest researcher


  1. Published

    Lessons learned from 40 novel PIGA patients and a review of the literature

    Bayat, A., Knaus, A., Pendziwiat, M., Afenjar, A., Stefan Barakat, T., Bosch, F., Callewaert, B., Calvas, P., Ceulemans, B., Chassaing, N., Depienne, C., Endziniene, M., Ferreira, C. R., Moura de Souza, C. F., Freihuber, C., Ganesan, S., Gataullina, S., Guerrini, R., Guerrot, A. M., Hansen, Lars, Jezela-Stanek, A., Karsenty, C., Kievit, A., Kooy, F. R., Korff, C. M., Kragh Hansen, J., Larsen, M., Layet, V., Lesca, G., McBride, K. L., Meuwissen, M., Mignot, C., Montomoli, M., Moore, H., Naudion, S., Nava, C., Nougues, M. C., Parrini, E., Pastore, M., Schelhaas, J. H., Skinner, S., Szczałuba, K., Thomas, A., Thomassen, M., Tranebjærg, Lisbeth, van Slegtenhorst, M., Wolfe, L. A., Lal, D., Gardella, E., Bomme Ousager, L., Brünger, T., Helbig, I., Krawitz, P. & Møller, R. S., 2020, In: Epilepsia. 61, 6, p. 1142-1155

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Published

    RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

    Farooq, Muhammad, Lindbæk, L., Krogh, Nicolai, Doganli, Canan, Keller, C., Mönnich, M., Gonçalves, A. B., Sakthivel, S., Mang, Yuan, Fatima, A., Andersen, V. S., Hussain, M. S., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Kjær, Klaus Wilbrandt, Gopalakrishnan, J., Pedersen, Lotte Bang, Møllgård, Kjeld, Nielsen, Henrik, Baig, S. M., Tommerup, Niels, Christensen, Søren Tvorup & Larsen, Lars Allan, 2020, In: Nature Communications. 11, 16 p., 5816.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    A mutation map for human glycoside hydrolase genes

    Hansen, Lars, Husein, D. M., Gericke, B., Hansen, Torben, Pedersen, Oluf Borbye, Tambe, M. A., Freeze, H. H., Naim, H. Y., Henrissat, B., Wandall, Hans H., Clausen, Henrik & Bennett, Eric Paul, 2020, In: Glycobiology. 30, 8, p. 500-515 16 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. 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

  5. Published

    Molecular basis for fibroblast growth factor 23 O-glycosylation by GalNAc-T3

    de las Rivas, M., Paul Daniel, E. J., Narimatsu, Y., Compañón, I., Kato, K., Hermosilla, P., Thureau, A., Ceballos-Laita, L., Coelho, H., Bernadó, P., Marcelo, F., Hansen, Lars, Maeda, R., Lostao, A., Corzana, F., Clausen, Henrik, Gerken, T. A. & Hurtado-Guerrero, R., 2020, In: Nature Chemical Biology. 16, p. 351–360

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 544414