Lars Hansen
Guest Researcher
Glycomics Program
Blegdamsvej 3
2200 København N.
Member of:
- 1987
- 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 journal › Journal article › peer-review
- 1991
- 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 journal › Journal article › peer-review
- 2005
- 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 › peer-review
- 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 › peer-review
- 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. 1275-1284Research output: Contribution to journal › Journal article › peer-review
- 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 journal › Journal article › peer-review
- 2006
- 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 › peer-review
- 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 › peer-review
- 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 journal › Journal article › peer-review
- 2007
- 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 journal › Journal article › peer-review
- 2008
- 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 › peer-review
- 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 › peer-review
- 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 journal › Journal article › peer-review
- 2009
- 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 › peer-review
- 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 › peer-review
- 2010
- 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 journal › Journal article › peer-review
- 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 journal › Journal article › peer-review
- 2011
- 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 › peer-review
- 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 › peer-review
- 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 journal › Journal article › peer-review
- 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 › peer-review
- 2012
- 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 › peer-review
- 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 › peer-review
- 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 journal › Journal article › peer-review
- 2013
- 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 journal › Journal article › peer-review
ID: 544414
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Precise integration of inducible transcriptional elements (PrIITE) enables absolute control of gene expression
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The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
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Display of the human mucinome with defined O-glycans by gene engineered cells
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