Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
ORCID: 0000-0002-4140-1578
1 - 4 out of 4Page size: 10
- 2002
- Published
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy
Thiselton, D. L., Alexander, C., Taanman, J. W., Brooks, S., Rosenberg, T., Eiberg, Hans Rudolf Lytchoff, Andreasson, S., Van Regemorter, N., Munier, F. L., Moore, A. T., Bhattacharya, S. S. & Votruba, M., 2002, In: Invest. Ophthalmol. Vis. Sci.. Vol. 43, p. 1715-1724Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic evidence that HNF-1α-dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function
Hansen, S. K., Párrizas, M., Jensen, M. L., Pruhova, S., Ek, J., Boj, S. F., Johansen, A., Maestro, M. A., Rivera, F., Eiberg, Hans Rudolf Lytchoff, Andel, M., Lebl, J., Pedersen, O., Ferrer, J. & Hansen, T., 2002, In: The Journal of Clinical Investigation. vol. 110, p. 827-833Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic evidence that HNF-1alpha-dependent transcriptional control of HNF-4alpha is essential for human pancreatic beta cell function
Hansen, S. K., Párrizas, M., Jensen, M. L., Pruhova, S., Ek, J., Boj, S. F., Johansen, A., Maestro, M. A., Rivera, F., Eiberg, Hans Rudolf Lytchoff, Andel, M., Lebl, J., Pedersen, Oluf Borbye, Ferrer, J. & Hansen, Torben, 2002, In: Journal of Clinical Investigation. 110, 6, p. 827-33 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract
Bu, L., Jin, Y., Shi, Y., Chu, R., Ban, A., Eiberg, Hans Rudolf Lytchoff, Andres, L., Jiang, H., Zheng, G., Qian, M., Cui, B., Xia, Y., Liu, J., Hu, L., Zhao, G., Hayden, M. R. & Kong, X., 2002, In: Nature Genetics. vol. 31, p. 276-278Research output: Contribution to journal › Journal article › Research › peer-review
ID: 5291
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Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity
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1878
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A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
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403
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Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
Research output: Contribution to journal › Letter › Research › peer-review
Published