Research graph
References from Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder. Local targets link to admitted publications; unresolved targets remain external evidence.
Prevalence and characteristics of autism spectrum disorder among children aged 8 years - Autism and developmental disabilities monitoring network, 11 sites, United States, 2018
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Dysregulation of multiple signaling neurodevelopmental pathways during embryogenesis: a possible cause of autism spectrum disorder
2021 · External reference
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10.1016/j.cell.2009.10.004 · External reference
The fragile X mutation impairs homeostatic plasticity in human neurons by blocking synaptic retinoic acid signaling
2018 · External reference
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10.1080/1028415x.2020.1809877 · External reference
10.1146/annurev-nutr-122319-034227
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10.1007/s11011-017-0049-6 · External reference
A rare De Novo RAI1 gene mutation affecting BDNF-enhancer-driven transcription activity associated with autism and atypical Smith-Magenis syndrome presentation
2018 · External reference
De Novo mutations of RERE cause a genetic syndrome with features that overlap those associated with proximal 1p36 deletions
10.1016/j.ajhg.2016.03.002 · 2016 · External reference
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10.1038/cr.2017.132 · External reference
10.1186/s11689-019-9268-y
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Prevalence of Autism spectrum disorder in china: a nationwide multi-center population-based study among children aged 6 to 12 years
10.1007/s12264-020-00530-6 · 2020 · External reference
Association between peripheral blood levels of vitamin A and Autism spectrum disorder in children: a meta-analysis
10.3389/fpsyt.2021.742937 · 2021 · External reference
Vitamin A and vitamin D deficiencies exacerbate symptoms in children with autism spectrum disorders
10.1080/1028415x.2017.1423268 · 2019 · External reference
Correlation between nutrition and symptoms: nutritional survey of children with autism spectrum disorder in chongqing, China
2016 · External reference
Vitamin A deficiency increases the risk of gastrointestinal comorbidity and exacerbates core symptoms in children with autism spectrum disorder
10.1038/s41390-020-0865-y · 2021 · External reference
Vitamin and mineral status of children with autism spectrum disorder in Hainan Province of China: associations with symptoms
10.1080/1028415x.2018.1558762 · 2020 · External reference
Nutritional status and symptoms in preschool children with Autism spectrum disorder: a two-center comparative study in Chongqing and Hainan Province, China
10.3389/fped.2020.00469 · 2020 · External reference
Vitamin A status is more commonly associated with symptoms and neurodevelopment in boys with autism spectrum disorders-a multicenter study in China
10.3389/fnut.2022.851980 · 2022 · External reference
Decreased levels of serum retinoic acid in chinese children with autism spectrum disorder
10.1016/j.psychres.2018.08.091 · 2018 · External reference
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Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort
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10.1016/j.neuron.2015.09.016 · External reference
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10.1016/j.celrep.2018.07.061 · External reference
10.1016/j.bbi.2022.02.027
10.1016/j.bbi.2022.02.027 · External reference
Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder
2017 · External reference
10.1016/j.ebiom.2022.104091
10.1016/j.ebiom.2022.104091 · External reference
10.1038/mp.2017.140
10.1038/mp.2017.140 · External reference
10.1038/s41380-018-0081-x
10.1038/s41380-018-0081-x · External reference
Vitamin A deficiency induces autistic-like behaviors in rats by regulating the RARβ-CD38-oxytocin axis in the hypothalamus
2018 · External reference
10.1016/j.neubiorev.2020.04.013
10.1016/j.neubiorev.2020.04.013 · External reference
10.1093/nar/28.1.27
10.1093/nar/28.1.27 · External reference
10.1093/nar/gkaa1113
10.1093/nar/gkaa1113 · External reference
Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans
2020 · External reference
AI-Driver: an ensemble method for identifying driver mutations in personal cancer genomes
10.1093/nargab/lqaa084 · 2020 · External reference
10.1093/nar/gkaa1033
10.1093/nar/gkaa1033 · External reference
Performance evaluation of pathogenicity-computation methods for missense variants
10.1093/nar/gky678 · 2018 · External reference
10.1093/nar/gkn835
10.1093/nar/gkn835 · External reference
10.1016/j.ajhg.2013.07.024
10.1016/j.ajhg.2013.07.024 · External reference
10.1038/s41586-020-2308-7
10.1038/s41586-020-2308-7 · External reference
Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders
10.1007/s12035-021-02377-y · 2021 · External reference
10.1186/2040-2392-4-36
10.1186/2040-2392-4-36 · External reference
10.1038/s41588-022-01148-2
10.1038/s41588-022-01148-2 · External reference
10.1038/s41588-022-01104-0
10.1038/s41588-022-01104-0 · External reference
10.1093/nar/gkaa1074
10.1093/nar/gkaa1074 · External reference
10.1038/nmeth.4083
10.1038/nmeth.4083 · External reference
10.1016/j.jgg.2021.03.002
10.1016/j.jgg.2021.03.002 · External reference
A scored human protein–protein interaction network to catalyze genomic interpretation
10.1038/nmeth.4083 · 2016 · External reference
10.1101/gr.1239303
10.1101/gr.1239303 · External reference
10.1089/omi.2011.0118
10.1089/omi.2011.0118 · External reference
Unresolved reference
External reference
10.1016/j.jgg.2018.09.002
10.1016/j.jgg.2018.09.002 · External reference
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10.1038/nature11396 · External reference
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10.1038/s41380-019-0454-9 · External reference
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10.1038/nature13772 · External reference
Neurodevelopmental disorders: elevated fetal sex steroids might confer risk for autism
10.1038/nrneurol.2014.107 · 2014 · External reference
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10.1038/mp.2014.48 · External reference
10.1056/nejme2110158
10.1056/nejme2110158 · External reference
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10.1038/330444a0 · External reference
Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN
2021 · External reference
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10.1038/s41467-021-23843-0 · External reference
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10.1038/s41380-020-0802-9 · External reference
10.1210/en.2017-00353
10.1210/en.2017-00353 · External reference
UBE3A: an E3 ubiquitin ligase with genome-wide impact in neurodevelopmental disease
10.3389/fnmol.2018.00476 · 2018 · External reference
Epilepsy-associated UBE3A deficiency downregulates retinoic acid signalling pathway
10.3389/fgene.2021.681295 · 2021 · External reference
Two distinct nuclear receptor interaction domains in NSD1, a novel SET protein that exhibits characteristics of both corepressors and coactivators.
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10.1074/jbc.274.48.34283 · External reference
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10.1038/mp.2013.146 · External reference
10.1016/j.cell.2016.10.031
10.1016/j.cell.2016.10.031 · External reference
Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism
10.1038/s41467-020-18526-1 · 2020 · External reference
Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes
10.1186/s13073-020-00785-8 · 2020 · External reference
10.1016/j.reprotox.2019.11.009
10.1016/j.reprotox.2019.11.009 · External reference
Association of maternal use of folic acid and multivitamin supplements in the periods before and during pregnancy with the risk of autism spectrum disorder in offspring
10.1001/jamapsychiatry.2017.4050 · 2018 · External reference
10.1371/journal.pone.0074849
10.1371/journal.pone.0074849 · External reference
Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder
10.1002/ajmg.b.32543 · 2017 · External reference
Developmental vitamin D and autism spectrum disorders: findings from the Stockholm Youth Cohort
10.1038/s41380-019-0578-y · 2021 · External reference
