Research output per year
Research output per year
Personal profile
Expertises
Genetics; Molecular Biology; Deafness; Hearing Loss; Diagnostics
Current research
Identification of novel genes and mechanisms that underlie hearing loss
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Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction
Reurink, J., Weisschuh, N., Garanto, A., Dockery, A., van den Born, L. I., Fajardy, I., Haer-Wigman, L., Kohl, S., Wissinger, B., Farrar, G. J., Ben-Yosef, T., Pfiffner, F. K., Berger, W., Weener, M. E., Dudakova, L., Liskova, P., Sharon, D., Salameh, M., Offenheim, A., Heon, E., & 30 others, 13 Apr 2023, In: HGG advances. 4, 2, 100181.Research output: Contribution to journal › Journal article › Research › peer-review
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A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene
Abdelfatah, N., Mostafa, A. A., French, C. R., Doucette, L. P., Penney, C., Lucas, M. B., Griffin, A., Booth, V., Rowley, C., Besaw, J. E., Tranebjærg, L., Rendtorff, N. D., Hodgkinson, K. A., Little, L. A., Agrawal, S., Parnes, L., Batten, T., Moore, S., Hu, P., Pater, J. A., & 8 others, Apr 2022, In: Human Genetics. 141, 3-4, p. 965-979 15 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients
Rendtorff, N. D., Karstensen, H. G., Lodahl, M., Tolmie, J., McWilliam, C., Bak, M., Tommerup, N., Nazaryan-Petersen, L., Kunst, H., Wong, M., Joss, S., Carelli, V. & Tranebjærg, L., 2 Sep 2022, In: Scientific Reports. 12, 1, 14959.Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in BCOR, a co-repressor of CRX/OTX2, are associated with early-onset retinal degeneration
Langouët, M., Jolicoeur, C., Javed, A., Mattar, P., Gearhart, M. D., Daiger, S. P., Bertelsen, M., Tranebjærg, L., Rendtorff, N. D., Grønskov, K., Jespersgaard, C., Chen, R., Sun, Z., Li, H., Alirezaie, N., Majewski, J., Bardwell, V. J., Sui, R., Koenekoop, R. K. & Cayouette, M., 9 Sep 2022, In: Science Advances. 8, 36, p. 1-20 20 p., eabh2868.Research output: Contribution to journal › Journal article › Research › peer-review
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Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder
Domínguez-Ruiz, M., Rodríguez-Ballesteros, M., Gandía, M., Gómez-Rosas, E., Villamar, M., Scimemi, P., Mancini, P., Rendtorff, N. D., Moreno-Pelayo, M. A., Tranebjaerg, L., Medà, C., Santarelli, R. & Del Castillo, I., 15 Jan 2022, In: Genes. 13, 1, p. 1-12 12 p., 149.Research output: Contribution to journal › Journal article › Research › peer-review
2 Citations (Scopus)