2016
Bon, B., Coe, B., Bernier, R., Green, C., Gerdts, J., Witherspoon, K., Kleefstra, T., Willemsen, M., Kumar, R., Fichera, M., Li, D., Amaral, D., Cristofoli, F., Peeters, H., Haan, E., Romano, C., Mefford, H., Scheffer, I., Gecz, J., de Vries, B., & Eichler, E. (2016). Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular Psychiatry. 21, 126–132
2015
Hudac, C.M., Kresse, A., Aaronson, B., DesChamps, T.D., Webb, S.J., & Bernier, R.A. (2015). Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications. Journal of Neurodevelopmental Disorders. 7(1):25
Krumm, N., Turner, T.N., Baker, C., Vives, L., Mohajeri, K., Witherspoon, K., Raja, A., Coe, B.P., Stessman, H.A., He, Z., Leal, S.M., Bernier, R., Eichler, E.E. (2015). Excess of rare, inherited truncating mutations in autism. Nature Genetics. 47(6):582-8
Higdon, R., Earl, R., Stanberry, L., Hudac, C., Montague, E., Stewart, E., Janko, I., Choineire, J., Broomall, W., Koler, N., Bernier, R., Kolker, E. (2015). The promise of multi-omics and clinical data integration to identify and target personalized health care approaches in ASD. OMICS: A Journal of Integrative Biology. 19(4):197-208
Upshaw, M., Bernier, R., Sommerville, J. (2015). Infants’ grip strength predicts mu rhythm attenuation during observation of lifting actions with weighted blocks. Developmental Science. 19(2):195-207
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