Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects

Por Lintas, Carla, Sacco, Roberto, Persico, Antonio M.
Publicado no J Neurodev Disord (2016)

Endocannabinoid Signaling in Autism

Por Chakrabarti, Bhismadev, Persico, Antonio, Battista, Natalia, Maccarrone, Mauro
Publicado no Neurotherapeutics (2015)

Urinary metabolomics of young Italian autistic children supports abnormal tryptophan and purine metabolism

Por Gevi, Federica, Zolla, Lello, Gabriele, Stefano, Persico, Antonio M.
Publicado no Mol Autism (2016)

Autism: Where Genetics Meets the Immune System

Por Persico, Antonio M., Van de Water, Judy, Pardo, Carlos A.
Publicado em 2012

Genetic Evidence Implicating Multiple Genes in the MET Receptor Tyrosine Kinase Pathway in Autism Spectrum Disorder

Por Campbell, Daniel B., Li, Chun, Sutcliffe, James S., Persico, Antonio M., Levitt, Pat
Publicado em 2008

Lack of Infection with XMRV or Other MLV-Related Viruses in Blood, Post-Mortem Brains and Paternal Gametes of Autistic Individuals

Por Lintas, Carla, Guidi, Francesco, Manzi, Barbara, Mancini, Antonio, Curatolo, Paolo, Persico, Antonio M.
Publicado em 2011

Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features

Por Lintas, Carla, Picinelli, Chiara, Piras, Ignazio S., Sacco, Roberto, Gabriele, Stefano, Verdecchia, Magda, Persico, Antonio M.
Publicado no Mol Syndromol (2016)

Methodological factors influencing measurement and processing of plasma reelin in humans

Por Lugli, Giovanni, Krueger, Jacqueline M, Davis, John M, Persico, Antonio M, Keller, Flavio, Smalheiser, Neil R
Publicado em 2003

Immune transcriptome alterations in the temporal cortex of subjects with autism

Por Garbett, Krassimira, Ebert, Philip J., Mitchell, Amanda, Lintas, Carla, Manzi, Barbara, Mirnics, Károly, Persico, Antonio M.
Publicado em 2008

P-cresol Alters Brain Dopamine Metabolism and Exacerbates Autism-Like Behaviors in the BTBR Mouse

Por Pascucci, Tiziana, Colamartino, Marco, Fiori, Elena, Sacco, Roberto, Coviello, Annalisa, Ventura, Rossella, Puglisi-Allegra, Stefano, Turriziani, Laura, Persico, Antonio M.
Publicado no Brain Sci (2020)

An Interstitial 17q11.2 de novo Deletion Involving the CDK5R1 Gene in a High-Functioning Autistic Patient

Por Lintas, Carla, Sacco, Roberto, Tabolacci, Claudio, Brogna, Claudia, Canali, Marco, Picinelli, Chiara, Tomaiuolo, Pasquale, Castronovo, Paola, Baccarin, Marco, Persico, Antonio M.
Publicado no Mol Syndromol (2019)

Age-Dependent Decrease and Alternative Splicing of Methionine Synthase mRNA in Human Cerebral Cortex and an Accelerated Decrease in Autism

Por Muratore, Christina R., Hodgson, Nathaniel W., Trivedi, Malav S., Abdolmaleky, Hamid M., Persico, Antonio M., Lintas, Carla, De La Monte, Suzanne, Deth, Richard C.
Publicado em 2013

A HOX Gene Mutation in a Family with Isolated Congenital Vertical Talus and Charcot-Marie-Tooth Disease

Por Shrimpton, Antony E., Levinsohn, E. Mark, Yozawitz, Justin M., Packard, Jr., David S., Cady, Robert B., Middleton, Frank A., Persico, Antonio M., Hootnick, David R.
Publicado em 2004

Reevaluation of Serum Arylesterase Activity in Neurodevelopmental Disorders

Por Piras, Ignazio Stefano, Gabriele, Stefano, Altieri, Laura, Lombardi, Federica, Sacco, Roberto, Lintas, Carla, Manzi, Barbara, Curatolo, Paolo, Nobile, Maria, Rigoletto, Catia, Molteni, Massimo, Persico, Antonio M.
Publicado no Antioxidants (Basel) (2021)

A genetic variant that disrupts MET transcription is associated with autism

Por Campbell, Daniel B., Sutcliffe, James S., Ebert, Philip J., Militerni, Roberto, Bravaccio, Carmela, Trillo, Simona, Elia, Maurizio, Schneider, Cindy, Melmed, Raun, Sacco, Roberto, Persico, Antonio M., Levitt, Pat
Publicado em 2006

Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder

Por Napolioni, Valerio, Ober-Reynolds, Benjamin, Szelinger, Szabolcs, Corneveaux, Jason J, Pawlowski, Traci, Ober-Reynolds, Sharman, Kirwan, Janet, Persico, Antonio M, Melmed, Raun D, Craig, David W, Smith, Christopher J, Huentelman, Matthew J
Publicado em 2013

Candidate gene study of <it>HOXB1 </it>in autism spectrum disorder

Por Muscarella Lucia A, Guarnieri Vito, Sacco Roberto, Curatolo Paolo, Manzi Barbara, Alessandrelli Riccardo, Giana Grazia, Militerni Roberto, Bravaccio Carmela, Lenti Carlo, Saccani Monica, Schneider Cindy, Melmed Raun, D'Agruma Leonardo, Persico Antonio M
Publicado em 2010-05-01

Candidate gene study of HOXB1 in autism spectrum disorder

Por Muscarella, Lucia A, Guarnieri, Vito, Sacco, Roberto, Curatolo, Paolo, Manzi, Barbara, Alessandrelli, Riccardo, Giana, Grazia, Militerni, Roberto, Bravaccio, Carmela, Lenti, Carlo, Saccani, Monica, Schneider, Cindy, Melmed, Raun, D'Agruma, Leonardo, Persico, Antonio M
Publicado em 2010

2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

Por Liu, Xudong, Malenfant, Patrick, Reesor, Chelsea, Lee, Alana, Hudson, Melissa L, Harvard, Chansonette, Qiao, Ying, Persico, Antonio M, Cohen, Ira L, Chudley, Albert E, Forster-Gibson, Cynthia, Rajcan-Separovic, Evica, Lewis, ME Suzanne, Holden, Jeanette JA
Publicado em 2011

Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1

Por Sacco, Roberto, Papaleo, Veruska, Hager, Jorg, Rousseau, Francis, Moessner, Rainald, Militerni, Roberto, Bravaccio, Carmela, Trillo, Simona, Schneider, Cindy, Melmed, Raun, Elia, Maurizio, Curatolo, Paolo, Manzi, Barbara, Pascucci, Tiziana, Puglisi-Allegra, Stefano, Reichelt, Karl-Ludvig, Persico, Antonio M
Publicado em 2007