Art

J-GLOBAL ID：201902237323115455   Reference number：19A2241580

Genetic Causes and Modifiers of Autism Spectrum Disorder

自閉症スペクトラム障害の遺伝的原因と修飾因子【JST・京大機械翻訳】

Author (2)： Rylaarsdam Lauren (Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States) ,  Guemez-Gamboa Alicia (Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States)
Material： Frontiers in Cellular Neuroscience (Web)
Volume： 13  Page： 385  Publication year： 2019 
JST Material Number： U7064A  ISSN： 1662-5102  Document type： Article
Article type： 文献レビュー  Country of issue： Switzerland (CHE)  Language： ENGLISH (EN)

Abstract/Point： Autism Spectrum Disorder (ASD)...

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Thesaurus term： child ,  spectrum ,  gene ,  human(primates) ,  copy number ,  *heredity ,  single nucleotide polymorphism ,  phenotype ,  therapy ,  communication ,  variation(biology)
Semi thesaurus term： 伝達経路 ,  化学修飾剤 ,  神経発達障害 ,  *自閉症スペクトラム障害 , 【Automatic Indexing@JST】

Author keywords (5)： autism spectrum disorder ,  genetic modifiers ,  CNV ,  epigenetics ,  gene-environment interaction

JST classification (2)： Nervous system diseases  (GN03000O) ,  Basic neurology  (GN01020W)

Reference (218)：

• Acuna-Hidalgo R., Bo T., Kwint M. P., van de Vorst M., Pinelli M., Veltman J. A., et al (2015). Post-zygotic point mutations are an underrecognized source of De Novo genomic variation. Am. J. Hum. Genet. 97 67-74. doi: 10.1016/j.ajhg.2015.05.008
• Al-Otaish H., Al-Ayadhi L., Bjørklund G., Chirumbolo S., Urbina M. A., El-Ansary A. (2018). Relationship between absolute and relative ratios of glutamate, glutamine and GABA and severity of autism spectrum disorder. Metab. Brain Dis. 33 843-854. doi: 10.1007/s11011-018-0186-6
• Amiet C., Gourfinkel-An I., Bouzamondo A., Tordjman S., Baulac M., Lechat P., et al (2008). Epilepsy in autism is associated with intellectual disability and gender: evidence from a meta-analysis. Biol. Psychiatry 64 577-582. doi: 10.1016/j.biopsych.2008.04.030
• Andrews S. V., Ellis S. E., Bakulski K. M., Sheppard B., Croen L. A., Hertz-Picciotto I., et al (2017). Cross-tissue integration of genetic and epigenetic data offers insight into autism spectrum disorder. Nat. Commun. 8:1011. doi: 10.1038/s41467-017-00868-y
• Artuso R., Papa F. T., Grillo E., Mucciolo M., Yasui D. H., Dunaway K. W., et al (2011). Investigation of modifier genes within copy number variations in Rett syndrome. J. Hum. Genet. 56 508-515. doi: 10.1038/jhg.2011.50

Terms in the title (3)： 自閉症スペクトラム障害 ,  遺伝 ,  原因