Center for the Molecular Biology of Neurosensory Systems

Fingerprint Dive into the research topics where Center for the Molecular Biology of Neurosensory Systems is active. These topic labels come from the works of this organization's members. Together they form a unique fingerprint.

Reading Medicine & Life Sciences
Dyslexia Medicine & Life Sciences
Genes Medicine & Life Sciences
Hearing Loss Medicine & Life Sciences
Language Medicine & Life Sciences
Chromosomes Medicine & Life Sciences
Quantitative Trait Loci Medicine & Life Sciences
Deafness Medicine & Life Sciences

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Research Output 1975 2019

1 Citation (Scopus)

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
Dyslexia
Genome-Wide Association Study
Attention Deficit Disorder with Hyperactivity
Reading
Genome
1 Citation (Scopus)

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
Genome-Wide Association Study
Hispanic Americans
African Americans
Reading
Epigenomics
1 Citation (Scopus)

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. D., 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

Exome
Deafness
RNA Splicing
RNA Splice Sites
Hearing Loss