Lars Hansen

Lars Hansen

senior adviser


  1. Published

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

    Jakobsen, L. P., 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 journalJournal articleResearchpeer-review

  2. Published
  3. Published

    Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents

    Khetarpal, S. A., Schjoldager, Katrine Ter-Borch Gram, Christoffersen, Christina, Raghavan, A., Edmondson, A. C., Reutter, H. M., Ahmed, B., Ouazzani, R., Peloso, G. M., Vitali, C., Zhao, W., Somasundara, A. V. H., Millar, J. S., Park, Y., Fernando, G., Livanov, V., Choi, S., Noé, E., Patel, P., Ho, S. P., Kirchgessner, T. G., Wandall, Hans H., Hansen, Lars, Bennett, Eric Paul, Vakhrushev, Sergey, Saleheen, D., Kathiresan, S., Brown, C. D., Abou Jamra, R., LeGuern, E., Clausen, Henrik & Rader, D. J., 9 Aug 2016, In : Cell Metabolism. 24, 2, p. 234-245 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG

    Kjær, Klaus Wilbrandt, Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Christensen, K. S., Opitz, J. M. & Tommerup, Niels, 2005, In : American Journal of Medical Genetics. Part A. 137, 2, p. 148-52 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2

    Kjær, Klaus Wilbrandt, Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hagen, C. B. V. D., Rosendahl, K., Tommerup, Niels & Mundlos, S., 2006, In : Journal of Medical Genetics. 43, 3, p. 225-231 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions

    Kjær, Klaus Wilbrandt, Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Utkus, A., Skovgaard, Lene Theil, Leicht, P., Opitz, J. M. & Tommerup, Niels, 2005, In : American Journal of Medical Genetics. Part A. 138, 4, p. 328-39 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published
  8. Published

    A novel mutation in IRF6 resulting in VWS-PPS spectrum disorder with renal aplasia

    Medeiros, F. D., Hansen, Lars, Mawlad, E., Eiberg, Hans Rudolf Lytchoff, Asklund, C., Tommerup, Niels & Jakobsen, L. P., 2008, In : American Journal of Medical Genetics. Part A. 146A, 12, p. 1605-1608 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. 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

  10. Published

    A validated gRNA library for CRISPR/Cas9 targeting of the human glycosyltransferase genome

    Narimatsu, Yoshiki, Joshi, Hiren Jitendra, Zhang, Y., Gomes, C., Chen, Y., Lorenzetti, F., Furukawa, S., Schjoldager, Katrine Ter-Borch Gram, Hansen, Lars, Clausen, Henrik, Bennett, Eric Paul & Wandall, Hans H., 2018, In : Glycobiology. 28, 5, p. 295–305

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 544414