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Comput."},{"issue":"12","key":"10.1016\/j.pneurobio.2025.102759_bib65","doi-asserted-by":"crossref","DOI":"10.1016\/j.celrep.2023.113533","article-title":"Cerebellar contribution to autism-relevant behaviors in fragile X syndrome models","volume":"42","author":"Gibson","year":"2023","journal-title":"Cell Rep."},{"issue":"7","key":"10.1016\/j.pneurobio.2025.102759_bib66","doi-asserted-by":"crossref","first-page":"795","DOI":"10.1038\/s10038-018-0451-x","article-title":"An estimation of the prevalence of genomic disorders using chromosomal microarray data","volume":"63","author":"Gillentine","year":"2018","journal-title":"J. Hum. Genet."},{"issue":"1","key":"10.1016\/j.pneurobio.2025.102759_bib67","doi-asserted-by":"crossref","first-page":"26","DOI":"10.1186\/s11689-019-9286-9","article-title":"Quantitative gait assessment in children with 16p11.2 syndrome","volume":"11","author":"Goldman","year":"2019","journal-title":"J. Neurodev. 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Disord."},{"issue":"7","key":"10.1016\/j.pneurobio.2025.102759_bib75","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0020912","article-title":"Aberrant immune responses in a mouse with behavioral disorders","volume":"6","author":"Heo","year":"2011","journal-title":"Plos One"},{"issue":"7","key":"10.1016\/j.pneurobio.2025.102759_bib76","doi-asserted-by":"crossref","first-page":"1999","DOI":"10.1177\/13623613211007717","article-title":"Autism spectrum disorder prevalence and associated sociodemographic factors in the school population: EPINED study","volume":"25","author":"Hidalgo","year":"2021","journal-title":"Autism"},{"key":"10.1016\/j.pneurobio.2025.102759_bib77","doi-asserted-by":"crossref","DOI":"10.1016\/j.neuropharm.2023.109634","article-title":"Serotonergic circuit dysregulation underlying autism-related phenotypes in BTBR mouse model of autism","volume":"237","author":"Higuchi","year":"2023","journal-title":"Neuropharmacology"},{"issue":"37","key":"10.1016\/j.pneurobio.2025.102759_bib78","doi-asserted-by":"crossref","first-page":"7321","DOI":"10.1523\/JNEUROSCI.3001-17.2019","article-title":"Sensorimotor cortical oscillations during movement preparation in 16p11.2 deletion carriers","volume":"39","author":"Hinkley","year":"2019","journal-title":"J. Neurosci."},{"issue":"2","key":"10.1016\/j.pneurobio.2025.102759_bib79","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1016\/j.biopsych.2016.08.036","article-title":"Astrocytic contributions to synaptic and learning abnormalities in a mouse model of fragile X syndrome","volume":"82","author":"Hodges","year":"2017","journal-title":"Biol. Psychiatry"},{"issue":"20","key":"10.1016\/j.pneurobio.2025.102759_bib80","doi-asserted-by":"crossref","first-page":"9335","DOI":"10.1073\/pnas.1002762107","article-title":"Region-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome","volume":"107","author":"Hoeft","year":"2010","journal-title":"Proc. Natl. Acad. Sci. USA"},{"issue":"41","key":"10.1016\/j.pneurobio.2025.102759_bib81","doi-asserted-by":"crossref","first-page":"17076","DOI":"10.1073\/pnas.1114042108","article-title":"Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism","volume":"108","author":"Horev","year":"2011","journal-title":"Proc. Natl. Acad. Sci. USA"},{"issue":"2","key":"10.1016\/j.pneurobio.2025.102759_bib82","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1111\/j.1469-7610.2004.00215.x","article-title":"Adult outcome for children with autism","volume":"45","author":"Howlin","year":"2004","journal-title":"J. Child Psychol. 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Biol."},{"issue":"1","key":"10.1016\/j.pneurobio.2025.102759_bib97","doi-asserted-by":"crossref","DOI":"10.1016\/j.celrep.2021.108932","article-title":"The autism-associated protein CHD8 is required for cerebellar development and motor function","volume":"35","author":"Kawamura","year":"2021","journal-title":"Cell Rep."},{"issue":"6","key":"10.1016\/j.pneurobio.2025.102759_bib98","doi-asserted-by":"crossref","first-page":"985","DOI":"10.3390\/ijms17060985","article-title":"RNA Secondary Structure Modulates FMRP's Bi-functional role in the MicroRNA pathway","volume":"17","author":"Kenny","year":"2016","journal-title":"Int. J. Mol. Sci."},{"issue":"22","key":"10.1016\/j.pneurobio.2025.102759_bib99","doi-asserted-by":"crossref","first-page":"12809","DOI":"10.1093\/nar\/gkac1134","article-title":"CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing","volume":"50","author":"Kerschbamer","year":"2022","journal-title":"Nucleic Acids Res."},{"issue":"4","key":"10.1016\/j.pneurobio.2025.102759_bib100","doi-asserted-by":"crossref","first-page":"624","DOI":"10.3390\/neurosci3040045","article-title":"Deficits in cerebellum-dependent learning and cerebellar morphology in male and female BTBR autism model mice","volume":"3","author":"Kiffmeyer","year":"2022","journal-title":"NeuroSci"},{"issue":"12","key":"10.1016\/j.pneurobio.2025.102759_bib101","doi-asserted-by":"crossref","first-page":"3342","DOI":"10.1111\/j.1460-9568.2008.06305.x","article-title":"Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome -: Mecp2 gene dosage effects and BDNF expression","volume":"27","author":"Kondo","year":"2008","journal-title":"Eur. 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Lett."},{"key":"10.1016\/j.pneurobio.2025.102759_bib128","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1016\/j.neubiorev.2016.12.037","article-title":"The BTBR mouse model of idiopathic autism - current view on mechanisms [Article; Proceedings Paper]","volume":"76","author":"Meyza","year":"2017","journal-title":"Neurosci. Biobehav. Rev."},{"issue":"2","key":"10.1016\/j.pneurobio.2025.102759_bib129","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/j.bbr.2011.11.004","article-title":"Fractone-associated N-sulfated heparan sulfate shows reduced quantity in BTBR T plus tf\/J mice: a strong model of autism","volume":"228","author":"Meyza","year":"2012","journal-title":"Behav. 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Neurosci."},{"issue":"16","key":"10.1016\/j.pneurobio.2025.102759_bib151","doi-asserted-by":"crossref","first-page":"1561","DOI":"10.1001\/jama.2019.14685","article-title":"Effect of fluoxetine on obsessive-compulsive behaviors in children and adolescents with autism spectrum disorders: a randomized clinical trial","volume":"322","author":"Reddihough","year":"2019","journal-title":"Jama-J. Am. Med. Assoc."},{"key":"10.1016\/j.pneurobio.2025.102759_bib152","first-page":"121","article-title":"Neurotrophic Factors in Mouse Models of Autism Spectrum Disorder: Focus on BDNF and IGF-1","volume":"224","author":"Reim","year":"2017"},{"issue":"11","key":"10.1016\/j.pneurobio.2025.102759_bib153","doi-asserted-by":"crossref","first-page":"886","DOI":"10.1016\/j.tins.2020.09.001","article-title":"16P11.2 Copy number variations and neurodevelopmental disorders","volume":"43","author":"Rein","year":"2020","journal-title":"Trends Neurosci."},{"issue":"1","key":"10.1016\/j.pneurobio.2025.102759_bib154","doi-asserted-by":"crossref","first-page":"165","DOI":"10.1007\/s00018-024-05185-4","article-title":"CRL4DCAF13 E3 ubiquitin ligase targets MeCP2 for degradation to prevent DNA hypermethylation and ensure normal transcription in growing oocytes","volume":"81","author":"Ren","year":"2024","journal-title":"Cell. Mol. Life Sci."},{"issue":"12","key":"10.1016\/j.pneurobio.2025.102759_bib155","doi-asserted-by":"crossref","first-page":"1670","DOI":"10.1038\/s41593-018-0270-6","article-title":"Characterization of human mosaic Rett syndrome brain tissue by single-nucleus RNA sequencing","volume":"21","author":"Renthal","year":"2018","journal-title":"Nat. Neurosci."},{"issue":"4","key":"10.1016\/j.pneurobio.2025.102759_bib156","doi-asserted-by":"crossref","first-page":"209","DOI":"10.1038\/s41583-021-00432-0","article-title":"The molecular biology of FMRP: new insights into fragile X syndrome","volume":"22","author":"Richter","year":"2021","journal-title":"Nat. Rev. Neurosci."},{"issue":"4","key":"10.1016\/j.pneurobio.2025.102759_bib157","doi-asserted-by":"crossref","DOI":"10.1093\/cercor\/bhae136","article-title":"Suppression of Cofilin function in the somatosensory cortex alters social contact behavior in the BTBR mouse inbred line","volume":"34","author":"Riemersma","year":"2024","journal-title":"Cereb. Cortex"},{"key":"10.1016\/j.pneurobio.2025.102759_bib158","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1016\/j.jpsychires.2018.10.014","article-title":"Neuroanatomical abnormalities in fragile X syndrome during the adolescent and young adult years","volume":"107","author":"Sandoval","year":"2018","journal-title":"J. Psychiatr. Res."},{"key":"10.1016\/j.pneurobio.2025.102759_bib159","doi-asserted-by":"crossref","first-page":"6","DOI":"10.3389\/fncir.2019.00006","article-title":"Shank3 transgenic and prenatal zinc-deficient autism mouse models show convergent and individual alterations of brain structures in MRI","volume":"13","author":"Schoen","year":"2019","journal-title":"Front. Neural Circuits"},{"key":"10.1016\/j.pneurobio.2025.102759_bib160","doi-asserted-by":"crossref","DOI":"10.3389\/fnins.2023.1087788","article-title":"Evaluating the effect of R-Baclofen and LP-211 on autistic behavior of the BTBR and Fmr1-KO mouse models","volume":"17","author":"Sharghi","year":"2023","journal-title":"Front. Neurosci."},{"issue":"8","key":"10.1016\/j.pneurobio.2025.102759_bib161","doi-asserted-by":"crossref","first-page":"562","DOI":"10.1176\/appi.ajp.21090896","article-title":"Subcortical brain development in autism and fragile X syndrome: evidence for dynamic, age- and disorder-specific trajectories in infancy","volume":"179","author":"Shen","year":"2022","journal-title":"Am. J. Psychiatry"},{"issue":"5","key":"10.1016\/j.pneurobio.2025.102759_bib162","doi-asserted-by":"crossref","first-page":"332","DOI":"10.1136\/jmg.2009.073015","article-title":"Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size","volume":"47","author":"Shinawi","year":"2010","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.pneurobio.2025.102759_bib163","doi-asserted-by":"crossref","DOI":"10.1038\/s41380-024-02491-y","article-title":"The complex etiology of autism spectrum disorder due to missense mutations of CHD8","author":"Shiraishi","year":"2024","journal-title":"Mol. Psychiatry"},{"issue":"4","key":"10.1016\/j.pneurobio.2025.102759_bib164","doi-asserted-by":"crossref","DOI":"10.1088\/1741-2552\/aa6b6b","article-title":"Electrophysiological signatures of atypical intrinsic brain connectivity networks in autism","volume":"14","author":"Shou","year":"2017","journal-title":"J. Neural Eng."},{"key":"10.1016\/j.pneurobio.2025.102759_bib165","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1016\/j.bbr.2016.02.015","article-title":"Ketogenic diet restores aberrant cortical motor maps and excitation-to-inhibition imbalance in the BTBR mouse model of autism spectrum disorder","volume":"304","author":"Smith","year":"2016","journal-title":"Behav. Brain Res."},{"key":"10.1016\/j.pneurobio.2025.102759_bib166","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1186\/2040-2392-4-18","article-title":"Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency","volume":"4","author":"Soorya","year":"2013","journal-title":"Mol. Autism"},{"issue":"5","key":"10.1016\/j.pneurobio.2025.102759_bib167","doi-asserted-by":"crossref","first-page":"2859","DOI":"10.1007\/s00415-024-12271-x","article-title":"CHD8-related disorders redefined: an expanding spectrum of dystonic phenotypes","volume":"271","author":"Sorrentino","year":"2024","journal-title":"J. Neurol."},{"issue":"13","key":"10.1016\/j.pneurobio.2025.102759_bib168","doi-asserted-by":"crossref","first-page":"1209","DOI":"10.1056\/NEJMoa1307491","article-title":"Patches of disorganization in the neocortex of children with autism","volume":"370","author":"Stoner","year":"2014","journal-title":"N. Engl. J. Med."},{"issue":"15","key":"10.1016\/j.pneurobio.2025.102759_bib169","doi-asserted-by":"crossref","first-page":"6209","DOI":"10.1523\/JNEUROSCI.4624-14.2015","article-title":"MeCP2 in the rostral striatum maintains local dopamine content critical for psychomotor control","volume":"35","author":"Su","year":"2015","journal-title":"J. Neurosci."},{"issue":"6","key":"10.1016\/j.pneurobio.2025.102759_bib170","doi-asserted-by":"crossref","first-page":"2192","DOI":"10.1093\/cercor\/bhy058","article-title":"Altered neocortical gene expression, brain overgrowth and functional over-connectivity in Chd8 haploinsufficient mice","volume":"28","author":"Suetterlin","year":"2018","journal-title":"Cereb. Cortex"},{"issue":"5","key":"10.1016\/j.pneurobio.2025.102759_bib171","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1001\/jamapsychiatry.2018.0180","article-title":"Development of white matter circuitry in infants with fragile X syndrome","volume":"75","author":"Swanson","year":"2018","journal-title":"Jama Psychiatry"},{"key":"10.1016\/j.pneurobio.2025.102759_bib172","doi-asserted-by":"crossref","DOI":"10.3389\/fphar.2023.1155729","article-title":"Seizure susceptibility to various convulsant stimuli in the BTBR mouse model of autism spectrum disorders","volume":"14","author":"Tallarico","year":"2023","journal-title":"Front. Pharmacol."},{"key":"10.1016\/j.pneurobio.2025.102759_bib173","doi-asserted-by":"crossref","first-page":"208","DOI":"10.1016\/j.neubiorev.2019.04.022","article-title":"Genetic mechanisms of regression in autism spectrum","volume":"102","author":"Tammimies","year":"2019","journal-title":"Neurosci. Biobehav. Rev."},{"issue":"15","key":"10.1016\/j.pneurobio.2025.102759_bib174","doi-asserted-by":"crossref","first-page":"2699","DOI":"10.1021\/acschemneuro.3c00260","article-title":"The Partial M1 Muscarinic Cholinergic Receptor Agonist, CDD-0102A, differentially modulates glutamate efflux in striatal subregions during stereotyped motor behavior in the BTBR mouse model of autism","volume":"14","author":"Teneqexhi","year":"2023","journal-title":"Acs Chem. Neurosci."},{"issue":"4","key":"10.1016\/j.pneurobio.2025.102759_bib175","doi-asserted-by":"crossref","first-page":"607","DOI":"10.1111\/ejn.15919","article-title":"Age-related behavioural and striatal dysfunctions in Shank3\u0394C\/\u0394C mouse model of autism spectrum disorder","volume":"57","author":"Thabault","year":"2023","journal-title":"Eur. J. Neurosci."},{"issue":"1","key":"10.1016\/j.pneurobio.2025.102759_bib176","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1038\/s41398-024-02947-3","article-title":"Pharmacological modulation of developmental and synaptic phenotypes in human SHANK3 deficient stem cell-derived neuronal models","volume":"14","author":"Thibaudeau","year":"2024","journal-title":"Transl. Psychiatry"},{"issue":"3","key":"10.1016\/j.pneurobio.2025.102759_bib177","first-page":"173","article-title":"MAPK cascade signalling and synaptic plasticity","volume":"5","author":"Thomas","year":"2004","journal-title":"Res. Support, Non-U. S. Gov. 't; ReS. Support, U. S. Gov. 't, P. H. S. ; Rev. ]. Nat. Rev. Neurosci."},{"issue":"16","key":"10.1016\/j.pneurobio.2025.102759_bib178","doi-asserted-by":"crossref","first-page":"8787","DOI":"10.3390\/ijms25168787","article-title":"Activation of the 5-HT1A receptor by eltoprazine restores mitochondrial and motor deficits in a Drosophila model of fragile X Syndrome","volume":"25","author":"Vannelli","year":"2024","journal-title":"Int. J. Mol. Sci."},{"issue":"1","key":"10.1016\/j.pneurobio.2025.102759_bib179","doi-asserted-by":"crossref","DOI":"10.1186\/s13229-020-00344-3","article-title":"Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors","volume":"11","author":"Varderidou-Minasian","year":"2020","journal-title":"Mol. 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Rep."},{"issue":"42","key":"10.1016\/j.pneurobio.2025.102759_bib183","doi-asserted-by":"crossref","first-page":"10911","DOI":"10.1523\/JNEUROSCI.1810-06.2006","article-title":"Dysregulation of brain-derived neurotrophic factor expression and neurosecretory function in Mecp2 null mice","volume":"26","author":"Wang","year":"2006","journal-title":"J. Neurosci."},{"issue":"23","key":"10.1016\/j.pneurobio.2025.102759_bib184","doi-asserted-by":"crossref","first-page":"4303","DOI":"10.1007\/s00213-015-4058-z","article-title":"Modulation of social deficits and repetitive behaviors in a mouse model of autism: the role of the nicotinic cholinergic system","volume":"232","author":"Wang","year":"2015","journal-title":"Psychopharmacology"},{"issue":"3","key":"10.1016\/j.pneurobio.2025.102759_bib185","doi-asserted-by":"crossref","first-page":"1819","DOI":"10.3390\/ijms24031819","article-title":"Autism spectrum disorder: neurodevelopmental risk factors, biological mechanism, and precision therapy","volume":"24","author":"Wang","year":"2023","journal-title":"Int. J. Mol. Sci."},{"issue":"3","key":"10.1016\/j.pneurobio.2025.102759_bib186","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1016\/j.nurt.2010.05.005","article-title":"Fragile X: leading the way for targeted treatments in autism","volume":"7","author":"Wang","year":"2010","journal-title":"Neurotherapeutics"},{"issue":"7","key":"10.1016\/j.pneurobio.2025.102759_bib187","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1056\/NEJMoa075974","article-title":"Association between microdeletion and microduplication at 16p11.2 and autism","volume":"358","author":"Weiss","year":"2008","journal-title":"N. Engl. J. Med."},{"issue":"5","key":"10.1016\/j.pneurobio.2025.102759_bib188","doi-asserted-by":"crossref","DOI":"10.1542\/peds.2020-011528","article-title":"Emergence of Developmental Delay in Infants and Toddlers With an FMR1 Mutation","volume":"147","author":"Wheeler","year":"2021","journal-title":"Pediatrics"},{"key":"10.1016\/j.pneurobio.2025.102759_bib189","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.neuropharm.2012.11.028","article-title":"Fragile X syndrome: from targets to treatments","volume":"68","author":"Wijetunge","year":"2013","journal-title":"Neuropharmacology"},{"issue":"6","key":"10.1016\/j.pneurobio.2025.102759_bib190","doi-asserted-by":"crossref","first-page":"460","DOI":"10.1352\/1944-7558-126.6.460","article-title":"Motor influences on communication: comparisons between down syndrome and fragile X syndrome","volume":"126","author":"Will","year":"2021","journal-title":"Ajidd-Am. J. Intellect. Dev. Disabil."},{"issue":"1","key":"10.1016\/j.pneurobio.2025.102759_bib191","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1186\/s11689-019-9281-1","article-title":"Developmental divergence: motor trajectories in children with fragile X syndrome with and without co-occurring autism","volume":"11","author":"Will","year":"2019","journal-title":"J. Neurodev. Disord."},{"key":"10.1016\/j.pneurobio.2025.102759_bib192","doi-asserted-by":"crossref","DOI":"10.1177\/13623613231225498","article-title":"Developmental associations between motor and communication outcomes in Fragile X syndrome: variation in the context of co-occurring autism","author":"Will","year":"2024","journal-title":"Autism"},{"issue":"1","key":"10.1016\/j.pneurobio.2025.102759_bib193","first-page":"76","article-title":"Thalamocortical dysconnectivity in autism spectrum disorder: an analysis of the autism brain imaging data exchange","volume":"2","author":"Woodward","year":"2017","journal-title":"Biol. Psychiatry-Cogn. 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