Channel:  Donders Institute for Brain, Cognition and Behaviour

640 Articles

A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss
de Bruijn, S. E., Smits, J. J., Liu, C., Lanting, C. P., Beynon, A. J., Blankevoort, j., Oostrik, J., Koole, W., de Vrieze, E., DOOFNL consortium, , Cremers, C. W., Cremers, F. P., Roosing, S., Yntema, H. G., Kunst, H. P., Zhao, B., Pennings, R. J., Kremer, H.
10.1101/2019.12.20.884726 — Posted: 2019-12-23
Resolving multisensory and attentional influences across cortical depth in sensory cortices
Gau, R., Bazin, P.-L., Trampel, R., Turner, R., Noppeney, U.
10.1101/548933 — Posted: 2019-12-21
Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.
Kummeling, J., Stremmelaar, D. E., Raun, N., Reijnders, M. R., Willemsen, M. H., Ruiterkamp-Versteeg, M., Schepens, M., Man, C. C., Gilissen, C., Cho, M. T., McWalter, K., Sinnema, M., Wheless, J. W., Simon, M. E., Genetti, C. A., Casey, A. M., Terhal, P. A., van der Smagt, J. `J, van Gassen, K. L., Joset, P., Bahr, A., Steindl, K., Rauch, A., Keller, E., Raas-Rothschild, A., Koolen, D. A., Agrawal, P. B., Hoffman, T. L., Powell-Hamilton, N. N., Thiffault, I., Engleman, K., Zhou, D., Bodamer, O., Hoefele, J., Riedhammer, K. M., Schwaibold, E. M., Tasic, V., Schubert, D., Top, D., Pfundt, R., H
10.1101/2019.12.17.879189 — Posted: 2019-12-18
Stimulus-modality independent activation of the brain network for language
Arana, S. L., Marquand, A. F., Hulten, A., Hagoort, P., Schoffelen, J. M.
10.1101/714998 — Posted: 2019-12-17
Gene Expression Correlates of the Cortical Network Underlying Sentence Processing
Kong, X.-Z., Tzourio-Mazoyer, N., Joliot, M., Fedorenko, E., Liu, J., Fisher, S. E., Francks, C.
10.1101/439984 — Posted: 2019-12-16
Susceptibility to auditory closed-loop stimulation of sleep slow oscillations changes with age
Schneider, J., Lewis, P. A., Koester, D., Born, J., Ngo, H.-V. V.
10.1101/2019.12.15.876847 — Posted: 2019-12-15
Exome-wide assessment of the functional impact and pathogenicity of multi-nucleotide mutations
Kaplanis, J., Akawi, N., Gallone, G., McRae, J. F., Prigmore, E., Wright, C. F., Fitzpatrick, D. R., Firth, H. V., Barrett, J. C., Hurles, M. E., on behalf of the Deciphering Developmental Disorders Study
10.1101/258723 — Posted: 2019-12-09
Characterizing neuroanatomic heterogeneity in people with and without ADHD based on subcortical brain volumes
Li, T., Rooij, D. v., Mota, N. R., Buitelaar, J. K., the ENIGMA ADHD Working Group, , Hoogman, M., Vasquez, A. A., Franke, B.
10.1101/868414 — Posted: 2019-12-08
An illustration of reproducibility in neuroscience research in the absence of selective reporting
Kong, X.-Z., ENIGMA Laterality Working Group, , Francks, C.
10.1101/866301 — Posted: 2019-12-06
Perinatal selective serotonin reuptake inhibitor exposure and behavioral outcomes: a systematic review and meta-analyses of animal studies
Ramsteijn, A. S., Van de Wijer, L., Rando, J., van Luijk, J., Homberg, J. R., Olivier, J. D. A.
10.1101/868265 — Posted: 2019-12-06

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