Lars Hansen

Lars Hansen

Guest Researcher

Member of:


    1. 2024
    2. 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 journalJournal articlepeer-review

    3. 2023
    4. Published

      A family with ulcerative colitis maps to 7p21.1 and comprises a region with regulatory activity for the aryl hydrocarbon receptor gene

      Eiberg, Hans Rudolf Lytchoff, Olsson, J. B., Bak, M., Bang-Berthelsen, C. H., Troelsen, J. T. & Hansen, Lars, 2023, In: European Journal of Human Genetics. 31, p. 1440-1446 7 p.

      Research output: Contribution to journalJournal articlepeer-review

    5. 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 journalJournal articlepeer-review

    6. 2022
    7. Published

      Installation of O-glycan sulfation capacities in human HEK293 cells for display of sulfated mucins

      Sun, L., Konstantinidi, Andriana, Ye, Z., Nason, R., Zhang, Y., Büll, Christian, Kahl-Knutson, B., Hansen, Lars, Leffler, H., Vakhrushev, Sergey, Yang, Zhang, Clausen, Henrik & Narimatsu, Yoshiki, 2022, In: Journal of Biological Chemistry. 298, 2, 101382.

      Research output: Contribution to journalJournal articlepeer-review

    8. 2021
    9. 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 journalJournal articlepeer-review

    10. 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 journalJournal articlepeer-review

    11. Published

      Polypeptide n-acetylgalactosaminyltransferase-associated phenotypes in mammals

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

      Research output: Contribution to journalReviewpeer-review

    12. 2020
    13. 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 articlepeer-review

    14. 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, L. & 34 others, 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 articlepeer-review

    15. Published

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

      de las Rivas, M., Paul Daniel, E. J., Narimatsu, Yoshiki, 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 articlepeer-review

    16. 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, L., Petäjä-Repo, U. E., Hintze, J. & 12 others, 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 articlepeer-review

    17. Published

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

      Farooq, M., Lindbæk, L., Krogh, N., Doganli, C., Keller, C., Mönnich, M., Gonçalves, A. B., Sakthivel, S., Mang, Y., Fatima, A., Andersen, V. S., Hussain, M. S., Eiberg, H., Hansen, L., Kjaer, K. W., Gopalakrishnan, J., Pedersen, L. B., Møllgård, K., Nielsen, H., Baig, S. M. & 3 others, Tommerup, Niels, Christensen, Søren Tvorup & Larsen, Lars Allan, 2020, In: Nature Communications. 11, 16 p., 5816.

      Research output: Contribution to journalJournal articlepeer-review

    18. 2019
    19. 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 journalJournal articlepeer-review

    20. 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 journalJournal articlepeer-review

    21. 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 journalJournal articlepeer-review

    22. Published

      The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells

      Tian, W., Ye, Z., Wang, S., Schulz, M. A., Van Coillie, Julie, Sun, L., Chen, Yen-Hsi, Narimatsu, Yoshiki, Hansen, Lars, Kristensen, C., Mandel, Ulla, Bennett, Eric Paul, Jabbarzadeh-Tabrizi, S., Schiffmann, R., Shen, J., Vakhrushev, Sergey, Clausen, Henrik & Yang, Zhang, 2019, In: Nature Communications. 10, 13 p., 1785.

      Research output: Contribution to journalJournal articlepeer-review

    23. 2018
    24. 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 journalJournal articlepeer-review

    25. Published
    26. Published
    27. Published

      Site-specific O-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactions

      Wang, S., Mao, Y., Narimatsu, Y., Ye, Z., Tian, W., Goth, C. K., Lira-Navarrete, E., Pedersen, N. B., Benito-Vicente, A., Martin, C., Uribe, K. B., Hurtado-Guerrero, R., Christoffersen, C., Seidah, N. G., Nielsen, R., Christensen, E. I., Hansen, L., Bennett, E. P., Vakhrushev, S. Y., Schjoldager, K. T. & 1 others, Clausen, Henrik, 2018, In: The Journal of Biological Chemistry. 293, 19, p. 7408 –7422

      Research output: Contribution to journalJournal articlepeer-review

    28. 2017
    29. 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 journalJournal articlepeer-review

    30. 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 journalConference abstract in journalpeer-review

    31. 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 journalJournal articlepeer-review

    32. 2016
    33. Published
    34. 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 journalJournal articlepeer-review

    35. Published

      A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family

      Farooq, M., Fatima, A., Mang, Y., Hansen, Lars, Kjaer, K. W., Baig, S. M., Larsen, Lars Allan & Tommerup, Niels, Mar 2016, In: Journal of Human Genetics. 61, 3, p. 271-273 3 p.

      Research output: Contribution to journalJournal articlepeer-review

    36. 2015
    37. Published

      A glycogene mutation map for discovery of diseases of glycosylation

      Hansen, Lars, Lind-Thomsen, A., Joshi, Hiren Jitendra, Pedersen, N. B., Have, C. T., Kong, Y., Wang, S., Sparso, T., Grarup, Niels, Vester-Christensen, M. B., Schjoldager, Katrine Ter-Borch Gram, Freeze, H. H., Hansen, Torben, Pedersen, Oluf Borbye, Henrissat, B., Mandel, Ulla, Clausen, Henrik, Wandall, Hans H. & Bennett, Eric Paul, 2015, In: Glycobiology. 25, 2, p. 211-224 14 p.

      Research output: Contribution to journalJournal articlepeer-review

    38. Published

      Fast and sensitive detection of indels induced by precise gene targeting

      Yang, Zhang, Steentoft, C., Hauge, C., Hansen, Lars, Thomsen, A. L., Niola, Francesco, Vester-Christensen, M. B., Frödin, Morten, Clausen, Henrik, Wandall, Hans H. & Bennett, Eric Paul, 2015, In: Nucleic Acids Research. 43, 9, p. 1-8 8 p., e59.

      Research output: Contribution to journalJournal articlepeer-review

    39. 2014
    40. Published

      The myosin chaperone UNC45B is involved in lens development and autosomal dominant juvenile cataract

      Hansen, Lars, Comyn, S., Mang, Y., Lind-Thomsen, A., Myhre, L., Jean, F., Eiberg, Hans Rudolf Lytchoff, Tommerup, Niels, Rosenberg, T. & Pilgrim, D., Nov 2014, In: European Journal of Human Genetics. 22, 11, p. 1290-1297 8 p.

      Research output: Contribution to journalJournal articlepeer-review

    41. 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 journalJournal articlepeer-review

    42. Published

      UDP-gal: BetaGlcNAc Beta 1,3-galactosyltransferase, polypeptide 1,2 (B3GALT1,2)

      Vester-Christensen, M. B., Hansen, Lars & Clausen, Henrik, 2014, Handbook of Glycosyltransferases and Related Genes, Second Edition. Springer, Vol. 1. p. 73-80 8 p.

      Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

    43. Published

      UDP-gal: BetaGal beta 1,3-galactosyltransferase polypeptide 6 (B3GALT6)

      Vester-Christensen, M. B., Hansen, Lars & Clausen, Henrik, 2014, Handbook of Glycosyltransferases and Related Genes. Springer, p. 101-108 8 p.

      Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

    44. 2013
    45. 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 journalJournal articlepeer-review

    46. 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 journalJournal articlepeer-review

    47. Published

      Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinism

      Grønskov, K., Dooley, C. M., Østergaard, Elsebet, Kelsh, R. N., Hansen, Lars, Levesque, M. P., Vilhelmsen, K., Møllgård, Kjeld, Stemple, D. L. & Rosenberg, T., 7 Mar 2013, In: American Journal of Human Genetics. 92, 3, p. 415-21 7 p.

      Research output: Contribution to journalJournal articlepeer-review

    48. 2012
    49. Published

      Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)

      Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Korbo, L., Nielsen, I., Svenstrup, K., Bech, S., Pinborg, L., Friberg, L., Hjermind, L., Olsen, O. & Nielsen, Jørgen Erik, Nov 2012, In: Clinical Genetics. 82, 3, p. 256-63 8 p.

      Research output: Contribution to journalJournal articlepeer-review

    50. 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 journalComment/debatepeer-review

    51. 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 journalJournal articlepeer-review

    52. 2011
    53. 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 journalJournal articlepeer-review

    54. 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 journalJournal articlepeer-review

    55. 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 journalJournal articlepeer-review

    56. Published

      RUNX2 analysis of Danish cleidocranial dysplasia families

      Hansen, Lars, Riis, A. K., Silahtaroglu, Asli, Hove, H., Lauridsen, E., Eiberg, Hans Rudolf Lytchoff & Kreiborg, Sven, 2011, In: Clinical Genetics. 79, 3, p. 254-63 10 p.

      Research output: Contribution to journalJournal articlepeer-review

    57. 2010
    58. Published

      Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS

      Farooq, M., Troelsen, J. T., Boyd, M., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hussain, M. S., Rehman, S. U., Azhar, A., Ali, A., Bakhtiar, S. M., Tommerup, Niels, Baig, S. M. & Kjaer, K. W., Jun 2010, In: European Journal of Human Genetics. 18, 6, p. 733-6 3 p.

      Research output: Contribution to journalJournal articlepeer-review

    59. Published

      A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family

      Anjum, I., Eiberg, Hans Rudolf Lytchoff, Baig, S. M., Tommerup, Niels & Hansen, Lars, Mar 2010, In: Molecular Vision. 16, p. 549-55 6 p.

      Research output: Contribution to journalJournal articlepeer-review

    60. 2009
    61. 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 journalJournal articlepeer-review

    62. 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 journalJournal articlepeer-review

    63. 2008
    64. 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 articlepeer-review

    65. 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 journalJournal articlepeer-review

    66. Published

      Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2

      Wissinger, B., Dangel, S., Jagle, H., Hansen, Lars, Baumann, B., Rudolph, G., Wolf, C., Bonin, M., Koeppen, K., Ladewig, T., Kohl, S., Zrenner, E. & Rosenberg, T., 2008, In: Investigative Ophthalmology & Visual Science. 49, 2, p. 751-757 6 p.

      Research output: Contribution to journalJournal articlepeer-review

    67. 2007
    68. Published

      Genetic heterogeneity in microcornea-cataract: Five novel mutations in CRYAA, CRYGD, and GJA

      Hansen, Lars, Yao, W. L., Eiberg, Hans Rudolf Lytchoff, Kjær, K. W., Baggesen, K., Hejtmancik, J. F. & Rosenberg, T., 2007, In: Investigative Ophthalmology & Visual Science. 48, 9, p. 3937-3944 7 p.

      Research output: Contribution to journalJournal articlepeer-review

    69. 2006
    70. 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 journalJournal articlepeer-review

    71. 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 journalJournal articlepeer-review

    72. 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 journalJournal articlepeer-review

    73. 2005
    74. Published

      Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1

      Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hansen, C., Mohr, J., Teglbjærg, P. S. & Kjaer, K. W., 15 Feb 2005, In: American Journal of Medical Genetics. 133 A, 1, p. 44-47 4 p.

      Research output: Contribution to journalJournal articlepeer-review

    75. 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 journalJournal articlepeer-review

    76. 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 journalJournal articlepeer-review

    77. 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 journalJournal articlepeer-review

    78. 1991
    79. Published

      The barley genes acl1 and Acl3 encoding acyl carrier proteins I and III are located on different chromosomes

      Hansen, Lars & von Wettstein-Knowles, P., Oct 1991, In: MGG Molecular & General Genetics. 229, 3, p. 467-478 12 p.

      Research output: Contribution to journalJournal articlepeer-review

    80. 1987
    81. 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 journalJournal articlepeer-review

    ID: 544414