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

nork Lintas, Carla, Sacco, Roberto, Persico, Antonio M.
Argitaratua izan da J Neurodev Disord (2016)

Genotype–phenotype correlation in Phelan‐McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes

nork Ricciardello, Arianna, Tomaiuolo, Pasquale, Persico, Antonio M.
Argitaratua izan da Am J Med Genet A (2021)

Endocannabinoid Signaling in Autism

nork Chakrabarti, Bhismadev, Persico, Antonio, Battista, Natalia, Maccarrone, Mauro
Argitaratua izan da Neurotherapeutics (2015)

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

nork Gevi, Federica, Zolla, Lello, Gabriele, Stefano, Persico, Antonio M.
Argitaratua izan da Mol Autism (2016)

Autism: Where Genetics Meets the Immune System

nork Persico, Antonio M., Van de Water, Judy, Pardo, Carlos A.
Argitaratua 2012

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

nork Campbell, Daniel B., Li, Chun, Sutcliffe, James S., Persico, Antonio M., Levitt, Pat
Argitaratua 2008

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

nork Lintas, Carla, Guidi, Francesco, Manzi, Barbara, Mancini, Antonio, Curatolo, Paolo, Persico, Antonio M.
Argitaratua 2011

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

nork Lintas, Carla, Picinelli, Chiara, Piras, Ignazio S., Sacco, Roberto, Gabriele, Stefano, Verdecchia, Magda, Persico, Antonio M.
Argitaratua izan da Mol Syndromol (2016)

Methodological factors influencing measurement and processing of plasma reelin in humans

nork Lugli, Giovanni, Krueger, Jacqueline M, Davis, John M, Persico, Antonio M, Keller, Flavio, Smalheiser, Neil R
Argitaratua 2003

Immune transcriptome alterations in the temporal cortex of subjects with autism

nork Garbett, Krassimira, Ebert, Philip J., Mitchell, Amanda, Lintas, Carla, Manzi, Barbara, Mirnics, Károly, Persico, Antonio M.
Argitaratua 2008

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

nork Pascucci, Tiziana, Colamartino, Marco, Fiori, Elena, Sacco, Roberto, Coviello, Annalisa, Ventura, Rossella, Puglisi-Allegra, Stefano, Turriziani, Laura, Persico, Antonio M.
Argitaratua izan da Brain Sci (2020)

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

nork Lintas, Carla, Sacco, Roberto, Tabolacci, Claudio, Brogna, Claudia, Canali, Marco, Picinelli, Chiara, Tomaiuolo, Pasquale, Castronovo, Paola, Baccarin, Marco, Persico, Antonio M.
Argitaratua izan da Mol Syndromol (2019)

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

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

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

nork 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.
Argitaratua 2004

Reevaluation of Serum Arylesterase Activity in Neurodevelopmental Disorders

nork 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.
Argitaratua izan da Antioxidants (Basel) (2021)

A genetic variant that disrupts MET transcription is associated with autism

nork 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
Argitaratua 2006

Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder

nork 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
Argitaratua 2013

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

nork 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
Argitaratua 2010-05-01

Candidate gene study of HOXB1 in autism spectrum disorder

nork 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
Argitaratua 2010

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

nork 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
Argitaratua 2011