Lars Hansen

Lars Hansen

Guest Researcher

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    1. Published

      A splice-site variant in the lncRNA gene RP1-140A9.1 cosegregates in the large Volkmann cataract family

      Eiberg, Hans Rudolf Lytchoff, Mikkelsen, Annemette Friis, Bak, M., Tommerup, Niels, Lund, A. M., Wenzel, Anne, Sabarinathan, R., Gorodkin, Jan, Bang-Berthelsen, C. H. & Hansen, Lars, 2019, In: Molecular Vision. 25, p. 1-11 11 p.

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

    2. Published

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

      Steentoft, C., Yang, Zhang, Wang, S., Ju, T., Vester-Christensen, M. B., Festari, M. F., King-Smith, S. L., Moremen, K., Larsen, I. S. B., Goth, C. K., Schjoldager, Katrine Ter-Borch Gram, Hansen, Lars, Bennett, Eric Paul, Mandel, Ulla & Narimatsu, Yoshiki, 2019, In: Glycobiology. 29, 9, p. 645–656 11 p.

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

    3. Published

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

      Narimatsu, Yoshiki, Joshi, Hiren Jitendra, Zhang, Y., Gomes, C., Chen, Yen-Hsi, 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 journal › Journal article › Research › peer-review

    4. Published

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

      Narimatsu, Y., Joshi, H. J., Nason, R., Van Coillie, J., Karlsson, R., Sun, L., Ye, Z., Chen, Y-H., Schjoldager, K. T., Steentoft, C., Furukawa, S., Bensing, B. A., Sullam, P. M., Thompson, A. J., Paulson, J. C., Büll, C., Adema, G. J., Mandel, U., Hansen, L., Bennett, E. P. & 4 others, Varki, A., Vakhrushev, Sergey, Yang, Zhang & Clausen, Henrik, 2019, In: Molecular Cell. 75, 2, p. 394-407, e1-e5

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

    5. 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., 6666.

      Research output: Contribution to journal › Comment/debate › Research › peer-review

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

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

    8. 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., Kjaer, K. W. & Hansen, Lars, 2008, In: Human Genetics. 123, 2, p. 177-87 10 p.

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

    9. Published

      Compound heterozygous ASPM mutations in Pakistani MCPH families

      Muhammad, F., 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 & Kjaer, K. W., 2009, In: American Journal of Medical Genetics. Part A. 149A, 5, p. 926-30 4 p.

      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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