Search Results - Schmötzer, G.

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders by Waltes, R., Duketis, E., Knapp, M., Anney, R., Huguet, G., Schlitt, S., Jarczok, T., Sachse, M., Kämpfer, L., Kleinböck, T., Poustka, F., Bolte, Sven, Schmötzer, G., Voran, A., Huy, E., Meyer, J., Bourgeron, T., Klauck, S., Freitag, C., Chiocchetti, A.

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Early developmental regression in autism spectrum disorder: Evidence from an international multiplex sample by Parr, J., Le Couteur, A., Baird, G., Rutter, M., Pickles, A., Fombonne, E., Bailey, A., Wallace, S., Wittemeyer, K., Monaco, A., Barnby, G., Bolton, P., Moore, J., Murin, M., McConachie, H., Berney, T., Docherty, Z., Abbs, S., Ogilvie, C., Warburton, P., Lamb, J., Green, J., Bolton, B., Packer, R., Haracopos, D., Pedersen, L., Isager, T., Brondum-Nielsen, K., Roge, B., Tauber, M., Mantoulan, C., Poustka, F., Bölte, Sven, Feineis-Matthews, S., Rühl, D., Schmötzer, G., Poustka, A., Klauck, S., Tsiantis, J., Papanikolaou, K., Maestrini, E., Van Engeland, H., De Jonge, M., Lord, C., Corsello, C., Cook, E., Salt, J., Guter, S., Leventhal, B., Volkmar, F., Koenig, K.

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