Lars Hansen

Lars Hansen

Guest Researcher

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    1. Published

      Dissecting structure-function of 3-O-sulfated heparin and engineered heparan sulfates

      Karlsson, R., Chopra, P., Joshi, A., Yang, Zhang, Vakhrushev, Sergey, Clausen, Thomas Mandel, Painter, C. D., Szekeres, G. P., Chen, Yen-Hsi, Sandoval, D. R., Hansen, Lars, Esko, J. D., Pagel, K., Dyer, D. P., Turnbull, Jeremy Ewan, Clausen, Henrik, Boons, G. J. & Miller, Rebecca Louise, 2021, In: Science Advances. 7, 52, eabl6026.

      Research output: Contribution to journal › Journal article › Research › peer-review

    2. Published

      Glycosyltransferase genes that cause monogenic congenital disorders of glycosylation are distinct from glycosyltransferase genes associated with complex diseases

      Joshi, Hiren Jitendra, Hansen, Lars, Narimatsu, Yoshiki, Freeze, H. H., Henrissat, B., Bennett, Eric Paul, Wandall, Hans H., Clausen, Henrik & Schjoldager, Katrine Ter-Borch Gram, 2018, In: Glycobiology. 28, 5, p. 284-294

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. Published

      500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip

      Jakobsen, Linda Plovmand, 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 journal › Journal article › Research › peer-review

    4. Published

      Genetic studies in congenital anterior midline cervical cleft

      Jakobsen, Linda Plovmand, Pfeiffer, P., Andersen, M., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Mang, Y., Bak, M., 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 journal › Journal article › Research › peer-review

    5. Published

      Isoform-specific mucin type O-glycosylation maintain epithelial homeostasis

      Bagdonaite, Ieva , E.M.H., P., K., L., Vakhrushev, Sergey, Hansen, Lars, Joshi, Hiren Jitendra, Bennett, Eric Paul, Dabelsteen, Sally & Wandall, Hans H., 2017, In: Glycoconjugate Journal. 34, Suppl. 1, p. S42 1 p., Abstract 78.

      Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

    6. Published

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

      Hansen, Lars, Tawamie, H., Murakami, Y., Mang, Y., ur Rehman, S., Buchert, R., Schaffer, S., Muhammad, S., Bak, M., 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 journal › Journal article › Research › peer-review

    7. Published

      The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46

      Hansen, Lars, Yao, W., Eiberg, Hans Rudolf Lytchoff, Funding, M., Riise, R., Kjær, K. W., Hejtmancik, J. F. & Rosenberg, T., 2006, In: Molecular Vision. 12, 116, p. 1033-1039 7 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    8. Published

      Three cDNA clones for barley leaf acyl carrier proteins I and III

      Hansen, Lars, Nov 1987, In: Carlsberg Research Communications. 52, 6, p. 381-392 12 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    9. Published

      Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified

      Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Barrett, T., Bek, T., Kjærsgaard, P., Tranebjærg, Lisbeth & Rosenberg, T., 2005, In: European Journal of Human Genetics. 13, 12, p. 1275-1284

      Research output: Contribution to journal › Journal article › Research › peer-review

    10. 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 journal › Journal article › Research › peer-review

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    ID: 544414