The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration

Gostic, M., Martinelli, A., Tucker, C., Yang, Z., Gasparoli, F. M., Ewart, J-Y., Dholakia, K., Sillar, K., Tello, J. & Paracchini, S., 1 Nov 2019, In: The Journal of Comparative Neurology. 527, 16, p. 2634-2643 10 p.

Research output: Contribution to journal › Article › peer-review

A rare missense variant in the ATP2C2 gene is associated with developmental language disorder (DLD)

Martinelli, A., Rice, M., Smith, S., Talcott, J., Stein, J., Kent, L., Hayiou-Thomas, M., Newbury, D., Hulme, C., Pitt, S. & Paracchini, S., 1 Dec 2020, In: European Journal of Human Genetics. 28, SUPPL 1, 1, p. 396-397 2 p.

Research output: Contribution to journal › Article › peer-review

Photostimulation for in vitro optogenetics with high power blue organic light-emitting diodes

Morton, A., Murawski, C., Deng, Y., Keum, C., Miles, G. B., Tello, J. A. & Gather, M. C., 18 Mar 2019, In: Advanced Biosystems. 3, 3, 8 p., 1800290.

Research output: Contribution to journal › Article › peer-review

Functional characterization of ATP2C2, a risk factor for language disorders

Martinelli, A., Diaz, R., Feliciotti, I., Pitt, S. & Paracchini, S., 2019, In: European Neuropsychopharmacology. 29, p. 1194-1195 2 p.

Research output: Contribution to journal › Abstract › peer-review

The DCDC2 deletion is not a risk factor for dyslexia

Scerri, T. S., Macpherson, E., Martinelli, A., Wa, W. C., Monaco, A. P., Stein, J., Zheng, M., Ho, C. S-H., McBride, C., Snowling, M., Hulme, C., Hayiou-Thomas, M. E., Waye, M. M. Y., Talcott, J. B. & Paracchini, S., 25 Jul 2017, In: Translational Psychiatry. 7, 7 p., e1182.

Research output: Contribution to journal › Article › peer-review

Functional characterization of ATP2C2, a risk factor for language disorders

Martinelli, A., Diaz, R., Feliciotti, I., Pitt, S. & Paracchini, S., 2019, In: European Neuropsychopharmacology. 29, p. 1194-1195 2 p.

Research output: Contribution to journal › Abstract › peer-review

IDENTIFICATION OF GENETIC INTERACTIONS INVOLVED IN DYSLEXIA PATHOGENESIS

Karbalai, N., Czamara, D., Moll, K., Ramus, F., Malik, R., Scerri, T. S., Schumacher, J., Morris, A. P., Bourgeron, T., Monaco, A. P., Paracchini, S., Fisher, S. E., Nothen, M., Schulte-Korne, G. & Muller-Myhsok, B., Oct 2017, In: European Neuropsychopharmacology. 27, p. S183-S184 2 p.

Research output: Contribution to journal › Abstract › peer-review

Stratified medicine for mental disorders

Schumann, G., Binder, E. B., Holte, A., de Kloet, E. R., Oedegaard, K. J., Robbins, T. W., Walker-Tilley, T. R., Bitter, I., Brown, V. J., Buitelaar, J., Ciccocioppo, R., Cools, R., Escera, C., Fleischhacker, W., Flor, H., Frith, C. D., Heinz, A., Johnsen, E., Kirschbaum, C., Klingberg, T. & 24 others, Lesch, K-P., Lewis, S., Maier, W., Mann, K., Martinot, J-L., Meyer-Lindenberg, A., Müller, C. P., Müller, W. E., Nutt, D. J., Persico, A., Perugi, G., Pessiglione, M., Preuss, U. W., Roiser, J. P., Rossini, P. M., Rybakowski, J. K., Sandi, C., Stephan, K. E., Undurraga, J., Vieta, E., van der Wee, N., Wykes, T., Haro, J. M. & Wittchen, H. U., 1 Jan 2014, In: European Neuropsychopharmacology. 24, 1, p. 5-50 46 p.

Research output: Contribution to journal › Article › peer-review

The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: further evidence and meta-analysis

Weber, H., Klamer, D., Freudenberg, F., Kittel-Schneider, S., Rivero, O., Scholz, C. -J., Volkert, J., Kopf, J., Heupel, J., Herterich, S., Adolfsson, R., Alttoa, A., Post, A., Grussendorf, H., Kramer, A., Gessner, A., Schmidt, B., Hempel, S., Jacob, C. P., Sanjuan, J. & 5 others, Molto, M. D., Lesch, K. -P., Freitag, C. M., Kent, L. & Reif, A., Jan 2014, In: European Neuropsychopharmacology. 24, 1, p. 65-85 21 p.

Research output: Contribution to journal › Article › peer-review