Lintas, Carla

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

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

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Gregory, S. G., Connelly, J. J., Towers, A. J., Johnson, J., Biscocho, D., Markunas, C. A., Lintas, C., Abramson, R. K., Wright, H. H., Ellis, P., et al. (2009) · BMC Medicine

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 576

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

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

Genome-wide expression studies in Autism spectrum disorder, Rett syndrome, and Down syndrome

Lintas, C., Sacco, R., & Persico, A. M. (2012) · Neurobiology of Disease

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 96

Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review

Castronovo, P., Baccarin, M., Ricciardello, A., Picinelli, C., Tomaiuolo, P., Cucinotta, F., Frittoli, M., Lintas, C., Sacco, R., & Persico, A. M. (2020) · Clinical Genetics

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 65

Linking genetics to epigenetics: The role of folate and folate‐related pathways in neurodevelopmental disorders

Lintas, C. (2019) · Clinical Genetics

Folate and B Vitamins ResearchEpigenetics and DNA Methylation

Cited by 62

Association of autism with polyomavirus infection in postmortem brains

Lintas, C., Altieri, L., Lombardi, F., Sacco, R., & Persico, A. M. (2010) · Journal of Neurovirology

Polyomavirus and related diseasesAutism Spectrum Disorder Research

Cited by 53

Decreased serum arylesterase activity in autism spectrum disorders

Gaita, L., Manzi, B., Sacco, R., Lintas, C., Altieri, L., Lombardi, F., Pawlowski, T. L., Redman, M., Craig, D. W., Huentelman, M. J., et al. (2010) · Psychiatry Research

Paraoxonase enzyme and polymorphismsAutism Spectrum Disorder Research

Cited by 39