C Bravaccio

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1

S. Puglisi‐Allegra, J. Hager, M. Elia, 2010, Molecular Psychiatry.

Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples.

A. Persico, R. Melmed, C. Bravaccio, 2000, American journal of medical genetics.

The predictive value of ABCB1, ABCG2, CYP3A4/5 and CYP2D6 polymorphisms for risperidone and aripiprazole plasma concentrations and the occurrence of adverse drug reactions

E. Clementi, M. Molteni, D. Cattaneo, 2017, The Pharmacogenomics Journal.

Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression

K. Mirnics, M. Elia, C. Lintas, 2009, Molecular Psychiatry.

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

T. Wassink, S. Puglisi‐Allegra, P. Gasparini, 2001, Molecular Psychiatry.