Lars Hansen

Lars Hansen

Guest Researcher

Member of:


    1. 1987
    2. 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

    3. 1991
    4. 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

    5. 2005
    6. 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

    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 journalJournal articlepeer-review

    8. 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

    9. 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

    10. 2006
    11. 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

    12. 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

    13. 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

    14. 2007
    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, 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

    16. 2008
    17. 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

    18. 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

    19. 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

    20. 2009
    21. 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

    22. 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

    23. 2010
    24. 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

    25. 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

    26. 2011
    27. 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

    28. 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

    29. 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

    30. 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

    31. 2012
    32. 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

    33. 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

    34. 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

    35. 2013
    36. 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

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