Lars Hansen

Lars Hansen

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    1. 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

    2. 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

    3. 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

    4. 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

    5. Published

      Polypeptide n-acetylgalactosaminyltransferase-associated phenotypes in mammals

      Kato, K., Hansen, Lars & Clausen, Henrik, 2021, In: Molecules. 26, 18, 5504.

      Research output: Contribution to journal › Review › Research › peer-review

    6. Published

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

      Khetarpal, S. A., Schjoldager, K. T., Christoffersen, C., 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. & 12 others, 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 journal › Journal article › Research › peer-review

    7. Published

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

      Kjaer, K. W., 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 journal › Journal article › Research › peer-review

    8. Published

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

      Kjær, K. W., 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 journal › Journal article › Research › peer-review

    9. Published

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

      Kjær, K. W., 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 journal › Journal article › Research › peer-review

    10. Published

      The SHDRA syndrome-associated gene TMEM260 encodes a protein-specific O-mannosyltransferase

      Larsen, I. S. B., Povolo, Lorenzo, Zhou, L., Tian, W., Mygind, Kasper Johansen, Hintze, John, Jiang, C., Hartill, V., Prescott, K., Johnson, C. A., Mullegama, S. V., McConkie-Rosell, A., McDonald, M., Hansen, Lars, Vakhrushev, Sergey, Schjoldager, Katrine Ter-Borch Gram, Clausen, Henrik, Worzfeld, T., Joshi, Hiren Jitendra & Halim, Adnan, 2023, In: Proceedings of the National Academy of Sciences of the United States of America. 120, 21, p. e2302584120

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

    11. Published

      Discovery of an O-mannosylation pathway selectively serving cadherins and protocadherins

      Larsen, I. S. B., Narimatsu, Yoshiki, Joshi, Hiren Jitendra, Siukstaite, L., Harrison, O. J., Brasch, J., Goodman, K. M., Hansen, Lars, Shapiro, L., Honig, B., Vakhrushev, Sergey, Clausen, Henrik & Halim, Adnan, 2017, In: Proceedings of the National Academy of Sciences of the United States of America. 114, 42, p. 11163-11168 6 p.

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

    12. Published

      De novo expression of human polypeptide N-acetylgalactosaminyltransferase 6 (GalNAc-T6) in colon adenocarcinoma inhibits the differentiation of colonic epithelium

      Lavrsen, K., Dabelsteen, Sally, Vakhrushev, Sergey, Levann, Asha Maria Rudjord, Haue, Amalie Dahl, Dylander, A., Mandel, Ulla, Hansen, Lars, Frödin, Morten, Bennett, Eric Paul & Wandall, Hans H., 2018, In: The Journal of Biological Chemistry. 293, p. 1298-1314

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

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

    14. 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

    15. 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

    16. E-pub ahead of print

      A family of di-glutamate mucin-degrading enzymes that bridges glycan hydrolases and peptidases

      Narimatsu, Yoshiki, Büll, Christian, Taleb, V., Liao, Q., Compañón, I., Sánchez-Navarro, D., Durbesson, F., Vincentelli, R., Hansen, Lars, Corzana, F., Rovira, C., Henrissat, B., Clausen, Henrik, Joshi, Hiren Jitendra & Hurtado-Guerrero, R., 2024, (E-pub ahead of print) In: Nature Catalysis.

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

    17. 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

    18. Published

      Display of the human mucinome with defined O-glycans by gene engineered cells

      Nason, R., Büll, C., Konstantinidi, A., Sun, L., Ye, Z., Halim, A., Du, W., Sørensen, D. M., Durbesson, F., Furukawa, S., Mandel, U., Joshi, H. J., Dworkin, L. A., Hansen, L., David, L., Iverson, T. M., Bensing, B. A., Sullam, P. M., Varki, A., Vries, E. D. & 6 others, de Haan, C. A. M., Vincentelli, R., Henrissat, B., Vakhrushev, Sergey, Clausen, Henrik & Narimatsu, Yoshiki, 2021, In: Nature Communications. 12, 1, 16 p., 4070.

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

    19. Published

      Regulation of protein O-glycosylation in epithelial cells - the polypeptide GalNAc-transferases direct cellular differentiation and maintenance of tissue homeostasis

      Pallesen, E. M., Bagdonaite, Ieva , Vakhrushev, Sergey, Hansen, Lars, Joshi, Hiren Jitendra, Dabelsteen, Sally & Wandall, Hans H., Dec 2016, In: Glycobiology. 26, 12, p. 1391-1391

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

    20. Published

      Precise integration of inducible transcriptional elements (PrIITE) enables absolute control of gene expression

      Pinto, R., Hansen, Lars, Hintze, John, Almeida, R., Larsen, S., Coskun, M., Davidsen, J., Mitchelmore, C., David, L., Troelsen, J. T. & Bennett, Eric Paul, 2017, In: Nucleic Acids Research. 45, 13, 15 p., e123.

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

    21. Published

      Immature truncated O-glycophenotype of cancer directly induces oncogenic features

      Radhakrishnan, P., Dabelsteen, S., Madsen, F. B., Francavilla, C., Kopp, K. L., Steentoft, C., Vakhrushev, S. Y., Olsen, J. V., Hansen, L., Bennett, E. P., Woetmann, A., Yin, G., Chen, L., Song, H., Bak, M., Hlady, R. A., Peters, S. L., Opavsky, R., Thode, C., Qvortrup, K. & 4 others, Schjoldager, Katrine Ter-Borch Gram, Clausen, Henrik, Hollingsworth, M. A. & Wandall, Hans H., 12 Aug 2014, In: Proceedings of the National Academy of Sciences of the United States of America. 111, 39, p. e4066-e4077 10 p.

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

    22. 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

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

    24. Published

      Genetic heterogeneity in Pakistani microcephaly families

      Sajid Hussain, M., Bakhtiar, S. M., Farooq, M., Anjum, I., Janzen, E., Reza Toliat, M., Eiberg, Hans Rudolf Lytchoff, Kjaer, K. W., 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 journal › Journal article › Research › peer-review

    25. 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

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    ID: 544414