Lisbeth Tranebjærg
Professor emeritus.
- 2011
- Published
Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss
Kokotas, H., Grigoriadou, M., Yang, L., Lodahl, M., Rendtorff, N. D., Gyftodimou, Y., Korres, G. S., Ferekidou, E., Kandiloros, D., Korres, S., Tranebjærg, L., Guan, M-X., Petersen, M. B., Kokotas, H., Grigoriadou, M., Li, Y., Lodahl, M., Rendtorff, N. D., Gyftodimou, Y., Korres, G. S. & 6 others, , 1 Jan 2011, In: International Journal of Pediatric Otorhinolaryngology. 75, 1, p. 89-94 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome
Koppelhus, U., Tranebjærg, Lisbeth, Esberg, G., Ramsing, M., Lodahl, M., Rendtorff, N. D., Olesen, H. V., Sommerlund, M., Koppelhus, U., Tranebjærg, Lisbeth, Esberg, G., Ramsing, M., Lodahl, M., Rendtorff, N. D., Olesen, H. V. & Sommerlund, M., 1 Mar 2011, In: Clinical and Experimental Dermatology. 36, 2, p. 142-8 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2012
- Published
"Mitochondrial diseases caused by mutations in inner membrane chaperone proteins"Book title: "Mitochondrial disorders Caused by Nuclear Genes"
Tranebjærg, Lisbeth, 2012, "Mitochondrial diseases causes by mutatons in inner membrane chaperone proteins". Wong, L-J. (ed.).Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review
- Published
Alterations in expression levels of deafness dystonia protein 1 affect mitochondrial morphology
Engl, G., Florian, S., Tranebjærg, Lisbeth & Rapaport, D., 2012, In: Human Molecular Genetics. 21, 2, p. 287-99 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Jervell and Lange-Nielsen Syndrome in: GeneReviews at GeneTests
Tranebjærg, Lisbeth, 2012, In: Medical Genetics Information Resource.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro)
Yuca, S. A., Rendtorff, N. D., Boulahbel, H., Lodahl, M., Tranebjærg, Lisbeth, Cesur, Y., Dogan, M., Yilmaz, C., Akgun, C. & Acikgoz, M., 2012, In: European Journal of Medical Genetics. 55, 1, p. 37-42 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome
Ha, A. D., Parratt, K. L., Rendtorff, N. D., Lodahl, M., Ng, K., Rowe, D. B., Sue, C. M., Hayes, M. W., Tranebjærg, Lisbeth & Fung, V. S. C., 2012, In: Movement Disorders. 27, 8, p. 1034-40 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in east Greenland
Homøe, Preben, Koch, A., Rendtorff, N. D., Lodahl, M., Andersen, T., Andersen, S., Eiberg, Hans Rudolf Lytchoff, Nielsen, I. & Tranebjærg, Lisbeth, Jun 2012, In: International Journal of Audiology. 51, 6, p. 433-6 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome
Bergman, J. E. H., Janssen, N., van der Sloot, A. M., de Walle, H. E. K., Schoots, J., Rendtorff, N. D., Tranebjærg, Lisbeth, Hoefsloot, L. H., van Ravenswaaij-Arts, C. M. A. & Hofstra, R. M. W., Aug 2012, In: Human Mutation. 33, 8, p. 1251-1260 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mutation update on the CHD7 gene involved in CHARGE syndrome
Janssen, N., Bergman, J. E. H., Swertz, M. A., Tranebjærg, Lisbeth, Lodahl, M., Schoots, J., Hofstra, R. M. W., van Ravenswaaij-Arts, C. M. A. & Hoefsloot, L. H., Aug 2012, In: Human Mutation. 33, 8, p. 1149-1160 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 1571395
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A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy
Research output: Contribution to journal › Journal article › Research › peer-review
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179
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Usher syndrome in Denmark: mutation spectrum and some clinical observations
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
156
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An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS
Research output: Contribution to journal › Journal article › Research › peer-review
Published