Persico, Antonio M.

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2018) · Cell

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 2,323

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2020) · Cell

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 2,321

Consensus Paper: Pathological Role of the Cerebellum in Autism

Fatemi, S. H., Aldinger, K. A., Ashwood, P., Bauman, M. L., Blaha, C. D., Blatt, G. J., Chauhan, A., Chauhan, V., Dager, S. R., Dickson, P. E., et al. (2012) · The Cerebellum

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 723

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Fu, J. M., Satterstrom, F. K., Peng, M., Brand, H., Collins, R. L., Dong, S., Wamsley, B., Klei, L., Wang, L., Hao, S. P., et al. (2022) · Nature Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 640

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

Persico, A. M., & Bourgeron, T. (2006) · Trends in Neurosciences

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 575

A genetic variant that disrupts MET transcription is associated with autism

Campbell, D. B., Sutcliffe, J. S., Ebert, P. J., Militerni, R., Bravaccio, C., Trillo, S., Elia, M., Schneider, C., Melmed, R., Sacco, R., et al. (2006) · Proceedings of the National Academy of Sciences

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 401

Immune transcriptome alterations in the temporal cortex of subjects with autism

Garbett, K., Ebert, P. J., Mitchell, A., Lintas, C., Manzi, B., Mirnics, K., & Persico, A. M. (2008) · Neurobiology of Disease

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 375

Blood serotonin levels in autism spectrum disorder: A systematic review and meta-analysis

Gabriele, S., Sacco, R., & Persico, A. M. (2014) · European Neuropsychopharmacology

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 346

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

Persico, A. M., D'Agruma, L., Maiorano, N., Totaro, A., Militerni, R., Bravaccio, C., Wassink, T. H., Schneider, C., Melmed, R., Trillo, S., et al. (2001) · Molecular Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 337

The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disorders

Loth, E., Charman, T., Mason, L., Tillmann, J., Jones, E. J. H., Wooldridge, C., Ahmad, J., Auyeung, B., Brogna, C., Ambrosino, S., et al. (2017) · Molecular Autism

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 299

Head circumference and brain size in autism spectrum disorder: A systematic review and meta-analysis

Sacco, R., Gabriele, S., & Persico, A. M. (2015) · Psychiatry Research: Neuroimaging

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 253

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

Gevi, F., Zolla, L., Gabriele, S., & Persico, A. M. (2016) · Molecular Autism

Autism Spectrum Disorder ResearchMetabolomics and Mass Spectrometry Studies

Cited by 251

Disruption of cerebral cortex MET signaling in autism spectrum disorder

Campbell, D. B., D'Oronzio, R., Garbett, K., Ebert, P. J., Mirnics, K., Levitt, P., & Persico, A. M. (2007) · Annals of Neurology

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 193

Urinary p-cresol in autism spectrum disorder

Persico, A. M., & Napolioni, V. (2013) · Neurotoxicology and Teratology

Autism Spectrum Disorder ResearchGut microbiota and health

Cited by 189

Stratified medicine for mental disorders

Schumann, G., Binder, E. B., Holte, A., de Kloet, E. R., Oedegaard, K. J., Robbins, T. W., Walker-Tilley, T. R., Bitter, I., Brown, V. J., Buitelaar, J., et al. (2014) · European Neuropsychopharmacology

Mental Health and PsychiatryMental Health Research Topics

Cited by 186

The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisation

Charman, T., Loth, E., Tillmann, J., Crawley, D., Wooldridge, C., Goyard, D., Ahmad, J., Auyeung, B., Ambrosino, S., Banaschewski, T., et al. (2017) · Molecular Autism

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 183

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

Lintas, C., & Persico, A. M. (2009) · Journal of Medical Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 178

Mitochondrial dysfunction in autism spectrum disorders: Cause or effect?

Palmieri, L., & Persico, A. M. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics

Autism Spectrum Disorder ResearchMitochondrial Function and Pathology

Cited by 173

Urinary p-cresol is elevated in small children with severe autism spectrum disorder

Altieri, L., Neri, C., Sacco, R., Curatolo, P., Benvenuto, A., Muratori, F., Santocchi, E., Bravaccio, C., Lenti, C., Saccani, M., et al. (2011) · Biomarkers

Autism Spectrum Disorder ResearchGut microbiota and health

Cited by 161

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

Campbell, D. B., Li, C., Sutcliffe, J. S., Persico, A. M., & Levitt, P. (2008) · Autism Research

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 154

Reelin Is a Serine Protease of the Extracellular Matrix

Quattrocchi, C. C., Wannenes, F., Persico, A. M., Ciafré, S. A., D'Arcangelo, G., Farace, M. G., & Keller, F. (2002) · Journal of Biological Chemistry

Axon Guidance and Neuronal SignalingProtease and Inhibitor Mechanisms

Cited by 154

Identification and validation of biomarkers for autism spectrum disorders

Loth, E., Spooren, W., Ham, L. M., Isaac, M. B., Auriche-Benichou, C., Banaschewski, T., Baron-Cohen, S., Broich, K., Bölte, S., Bourgeron, T., et al. (2016) · Nature Reviews Drug Discovery

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 140

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions

D'Amelio, M., Ricci, I., Sacco, R., Liu, X., D'Agruma, L., Muscarella, L. A., Guarnieri, V, Militerni, R., Bravaccio, C., Elia, M., et al. (2005) · Molecular Psychiatry

Paraoxonase enzyme and polymorphismsAutism Spectrum Disorder Research

Cited by 125

Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum Disorder

Tillmann, J., Ashwood, K., Absoud, M., Bölte, S., Bonnet-Brilhault, F., Buitelaar, J. K., Calderoni, S., Calvo, R., Canal-Bedia, R., Canitano, R., et al. (2018) · Journal of Autism and Developmental Disorders

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 121