Center for the Molecular Biology of Neurosensory Systems

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  • Network Recent external collaboration on country level. Dive into details by clicking on the dots.

    Research Output

    Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

    Gialluisi, A., Andlauer, T. F. M., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., Ludwig, K. U., Czamara, D., St Pourcain, B., Brandler, W., Honbolygó, F., Tóth, D., Csépe, V., Huguet, G., Morris, A. P., Hulslander, J., Willcutt, E. G., DeFries, J. C., Olson, R. K., Smith, S. D. & 25 others, Pennington, B. F., Vaessen, A., Maurer, U., Lyytinen, H., Peyrard-Janvid, M., Leppänen, P. H. T., Brandeis, D., Bonte, M., Stein, J. F., Talcott, J. B., Fauchereau, F., Wilcke, A., Francks, C., Bourgeron, T., Monaco, A. P., Ramus, F., Landerl, K., Kere, J., Scerri, T. S., Paracchini, S., Fisher, S. E., Schumacher, J., Nöthen, M. M., Müller-Myhsok, B. & Schulte-Körne, G., Dec 1 2019, In : Translational Psychiatry. 9, 1, 77.

    Research output: Contribution to journalArticle

    Open Access
  • 8 Scopus citations

    Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth

    Pediatric, Imaging, Neurocognition, and Genetics Consortium, Aug 1 2019, In : Journal of medical genetics. 56, 8, p. 557-566 10 p.

    Research output: Contribution to journalArticle

    Open Access
  • 3 Scopus citations

    Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

    Booth, K. T., Askew, J. W., Talebizadeh, Z., Huygen, P. L. M., Eudy, J., Kenyon, J., Hoover, D., Hildebrand, M. S., Smith, K. R., Bahlo, M., Kimberling, W. J., Smith, R. J. H., Azaiez, H. & Smith, S. D., Apr 1 2019, In : Genetics in Medicine. 21, 4, p. 948-954 7 p.

    Research output: Contribution to journalArticle

  • 10 Scopus citations