Research output per year
Research output per year
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Dive into the research topics where Lisbeth Tranebjærg is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Research output
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Novel HARS2 missense variants identified in individuals with sensorineural hearing impairment and Perrault syndrome
Karstensen, H. G., Rendtorff, N. D., Hindbæk, L. S., Colombo, R., Stein, A., Birkebæk, N. H., Hartmann-Petersen, R., Lindorff-Larsen, K., Højland, A. T., Petersen, M. B. & Tranebjærg, L., Mar 2020, In: European Journal of Medical Genetics. 6 p., 103733.Research output: Contribution to journal › Journal article › Research › peer-review
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Partial trisomy 21 map: Ten cases further supporting the highly restricted Down syndrome critical region (HR-DSCR) on human chromosome 21
Pelleri, M. C., Cicchini, E., Petersen, M. B., Tranebjærg, L., Mattina, T., Magini, P., Antonaros, F., Caracausi, M., Vitale, L., Locatelli, C., Seri, M., Strippoli, P., Piovesan, A. & Cocchi, G., Aug 2019, In: Molecular Genetics & Genomic Medicine. 7, 14 p., e797.Research output: Contribution to journal › Journal article › Research › peer-review
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Adaptive Processes in Hearing
Santurette, S., Christensen-Dalsgaard, J., Tranebjærg, L., Andersen, T., Poulsen, T. & Dau, T., 2018, In: Trends in Hearing. 22, p. 1-2 2331216518762261.Research output: Contribution to journal › Editorial
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Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome
Xu, L., Jensen, H., Johnston, J. J., Di Maria, E., Kloth, K., Cristea, I., Sapp, J. C., Darling, T. N., Huryn, L. A., Tranebjærg, L., Cinotti, E., Kubisch, C., Rødahl, E., Bruland, O., Biesecker, L. G., Houge, G. & Bredrup, C., 2018, In: American Journal of Human Genetics. 103, 6, p. 976-983 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management
Tranebjærg, L., Strenzke, N., Lindholm, S., Rendtorff, N. D., Poulsen, H., Khandelia, H., Kopec, W., Lyngbye, T. J. B., Hamel, C., Delettre, C., Bocquet, B., Bille, M., Owen, H. H., Bek, T., Jensen, H., Østergaard, K., Möller, C., Luxon, L., Carr, L. & Wilson, L. & 11 others, , 2018, In: Human Genetics. 137, 2, p. 111-127 17 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct
Chattaraj, P., Munjal, T., Honda, K., Rendtorff, N. D., Ratay, J. S., Muskett, J. A., Risso, D. S., Roux, I., Gertz, E. M., Schäffer, A. A., Friedman, T. B., Morell, R. J., Tranebjærg, L. & Griffith, A. J., 2017, In: Journal of Medical Genetics. 54, 10, p. 665-673 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy
Zazo Seco, C., Castells-Nobau, A., Joo, S.-H., Schraders, M., Foo, J. N., van der Voet, M., Velan, S. S., Nijhof, B., Oostrik, J., de Vrieze, E., Katana, R., Mansoor, A., Huynen, M., Szklarczyk, R., Oti, M., Tranebjærg, L., van Wijk, E., Scheffer-de Gooyert, J. M., Siddique, S. & Baets, J. & 10 others, , 1 Feb 2017, In: Disease models & mechanisms. 10, p. 105-118 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
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An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS
Tracewska-Siemiątkowska, A., Haer-Wigman, L., Bosch, D. G. M., Nickerson, D., Bamshad, M. J., van de Vorst, M., Rendtorff, N. D., Möller, C., Kjellström, U., Andréasson, S., Cremers, F. P. M., Tranebjærg, L. & University of Washington Center for Mendelian Genomics, 11 Dec 2017, In: Genes. 8, 12, 9 p., 381.Research output: Contribution to journal › Journal article › Research › peer-review