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Pervasive alterations of intra-axonal volume and network organization in young children with a 16p11.2 deletion.

• Authors : Maillard, A.M.; Romascano, D.; Villalón-Reina, J.E.

Subjects: Child; Humans; Animals

• Source: Translational psychiatry, vol. 14, no. 1, pp. 95

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Autism Spectrum Disorder Genetics: Diverse Genes with Diverse Clinical Outcomes

• Authors : Talkowski, Michael E; Minikel, Eric V; Gusella, James F

• Source: Harvard Review of Psychiatry, 22(2), 65-75, (2017-09-26)

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Genetic and environmental architecture of synaesthesia and its association with the autism spectrum-a twin study

• Authors : Taylor, Mark J; van Leeuwen, Tessa; Kuja-Halkola, Ralf

Subjects: Humans; Adolescent; Autistic Disorder

• Source: Taylor , M J , van Leeuwen , T , Kuja-Halkola , R , Lundström , S , Larsson , H , Lichtenstein , P , Bölte , S & Neufeld , J 2023 , ' Genetic and environmental architecture of synaesthesia and its

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Multi-level analysis of the gut-brain axis shows autism spectrum disorder-associated molecular and microbial profiles.

• Authors : Morton, J.T.; Jin, D.M.; Mills, R.H.

Subjects: Humans; Gastrointestinal Microbiome/genetics; Brain-Gut Axis

• Source: Nature neuroscience, vol. 26, no. 7, pp. 1208-1217

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Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome.

• Authors : Jain, P.; Miller-Fleming, T.; Topaloudi, A. ...

Subjects: Male; Female; Humans

• Source: Translational psychiatry, vol. 13, no. 1, pp. 69

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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant

• Authors : Aerden, Mio; Denommé-Pichon, Anne Sophie; Bonneau, Dominique

Subjects: Autism Spectrum Disorder/genetics; Carrier Proteins/genetics; Humans

• Source: Aerden , M , Denommé-Pichon , A S , Bonneau , D , Bruel , A L , Delanne , J , Gérard , B , Mazel , B , Philippe , C , Pinson , L , Prouteau , C , Putoux , A , Tran Mau-Them , F , Viora-Dupont , É ,

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Integrated exome and transcriptome analysis prioritizes MAP4K4 de novo frameshift variants in autism spectrum disorder as a novel disease–gene association

• Authors : Cesana, M.; Vaccaro, L.; Larsen, M. J.

Subjects: Autism Spectrum Disorder/genetics; Exome; Frameshift Mutation

• Source: Cesana , M , Vaccaro , L , Larsen , M J , Kibæk , M , Micale , L , Riccardo , S , Annunziata , P , Colantuono , C , Di Filippo , L , De Brasi , D , Castori , M , Fagerberg , C , Acquaviva , F &

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Immune activation during pregnancy exacerbates ASD-related alterations in Shank3-deficient mice.

• Authors : Atanasova, Ekaterina; Arévalo, Andrea Pérez; Graf, Ines

Subjects: info:eu-repo/classification/ddc/610; Female; PregnancyDE

• Source: Molecular autism 14(1), 1 (2023). doi:10.1186/s13229-022-00532-3

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Shank3 deletion in PV neurons is associated with abnormal behaviors and neuronal functions that are rescued by increasing GABAergic signaling.

• Authors : Pagano, Jessica; Landi, Silvia; Sala, Carlo

Subjects: info:eu-repo/classification/ddc/610; Mice; AnimalsDE

• Source: Molecular autism 14(1), 28 (2023). doi:10.1186/s13229-023-00557-2

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Cell-type-specific disruption of cortico-striatal circuitry drives repetitive patterns of behavior in fragile X syndrome model mice.

• Authors : Longo, F.; Aryal, S.; Anastasiades, P.G.

Subjects: Animals; Humans; Mice

• Source: Cell reports, vol. 42, no. 8, pp. 112901

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