Lars Hansen

Lars Hansen

senior adviser


  1. 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 articleResearchpeer-review

  2. Published

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

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

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. 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., Kjær, Klaus Wilbrandt & Hansen, Lars, 2008, In : Human Genetics. 123, 2, p. 177-87 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. 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. & Kjær, Klaus Wilbrandt, 15 Feb 2005, In : American Journal of Medical Genetics. 133 A, 1, p. 44-47 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 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, Mads, 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 articleResearchpeer-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 journalJournal articleResearchpeer-review

  7. Published

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

    Farooq, Muhammad, Fatima, A., Mang, Yuan, Hansen, Lars, Kjær, Klaus Wilbrandt, 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 journalComment/debateResearchpeer-review

  8. 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, Muhammad, 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. & Kjær, Klaus Wilbrandt, Jun 2010, In : European Journal of Human Genetics. 18, 6, p. 733-6 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. 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 articleResearchpeer-review

  10. Published

    RUNX2 analysis of Danish cleidocranial dysplasia families

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

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

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

    Hansen, Lars, Tawamie, H., Murakami, Y., Mang, Yuan, ur Rehman, S., Buchert, R., Schaffer, S., Muhammad, S., Bak, Mads, 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 articleResearchpeer-review

  12. Published

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

    Hansen, Lars, Comyn, S., Mang, Yuan, 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 articleResearchpeer-review

  13. 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 articleResearchpeer-review

  14. 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.

    Research output: Contribution to journalLetterResearchpeer-review

  15. Published

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

    Hansen, Lars, Yao, W. L., Eiberg, Hans Rudolf Lytchoff, Kjær, Klaus Wilbrandt, 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 articleResearchpeer-review

  16. 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, Klaus Wilbrandt, Hejtmancik, J. F. & Rosenberg, T., 2006, In : Molecular Vision. 12, 116, p. 1033-1039 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. 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 articleResearchpeer-review

  18. 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 articleResearchpeer-review

  19. 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 journalResearchpeer-review

  20. Published

    Genetic studies in congenital anterior midline cervical cleft

    Jakobsen, L. P., Pfeiffer, P., Andersen, M., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Mang, Yuan, Bak, Mads, 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 articleResearchpeer-review

  21. 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

  22. Published
  23. 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

  24. 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

  25. 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

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