NRN1 Gene as a Potential Marker of Early-Onset Schizophrenia: Evidence from Genetic and Neuroimaging Approaches

by Almodóvar-Payá, C., Arias, B., Callado, L.F, Carrión, M.I, Cuesta, M.J, Fañanás, L., Fatjó-Vilas, M., Gallego, C., Giralt-López, M., Guardiola-Ripoll, M., Guerrero-Pedraza, A., Lázaro, L., Maristany, T., Miret, S., Muñoz, M.J, Parellada, M., Pomarol-Clotet, E., Salgado-Pineda, P., Salvador, R., Sarró, S.
Published 2022

Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease

by Barbero, P., Berenstein, A., Bidondo, M.P, Brun, P., Bruque, C.D, Cosentino, V., Dain, L., Delea, M., Espeche, L.D, Fabro, M., Fernández, C.S, Furforo, L., Galain, M., Groisman, B., Izquierdo, A., Kolomenski, J.E, Liascovich, R., Martinoli, C., Massara, L.S, Mendez, R., Oliveri, J., on behalf of the PID ACM-CC Group, Rittler, M., Rozental, S., Taboas, M., Vilas, M.
Published 2022