Antonio M. Persico

Using genetic findings in autism for the development of new pharmaceutical compounds

J. Glennon, R. Jagasia, J. Buitelaar, 2013, Psychopharmacology.

Slow intestinal transit contributes to elevate urinary p‐cresol level in Italian autistic children

A. Urbani, R. Sacco, M. P. Riccio, 2016, Autism research : official journal of the International Society for Autism Research.

A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies TaqI RFLPs

G. Uhl, E. Jabs, C. Griffin, 1993, FEBS letters.

Brain transcription factor gene expression, neurotransmitter levels, and novelty response behaviors: Alterations during rat amphetamine withdrawal and following chronic injection stress

G. Uhl, A. Persico, C. Schindler, 1995, Synapse.

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

R. Schmidt, Candace Patterson, Stephan J. Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .