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Shared sociogenetic basis of honey bee behavior and human risk for autism.

作者信息

Crespi Bernard J

机构信息

Department of Biological Sciences, Simon Fraser University, Burnaby, BC, Canada V5A 1S6

出版信息

Proc Natl Acad Sci U S A. 2017 Sep 5;114(36):9502-9504. doi: 10.1073/pnas.1712292114. Epub 2017 Aug 29.

DOI:10.1073/pnas.1712292114
PMID:28851832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5594702/
Abstract
摘要

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Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD.多基因风险评分和遗传力估计揭示了 ASD 和 OCD 之间的遗传关系。
Eur Neuropsychopharmacol. 2017 Jul;27(7):657-666. doi: 10.1016/j.euroneuro.2017.03.011.
3
Advancing the understanding of autism disease mechanisms through genetics.通过遗传学增进对自闭症疾病机制的理解。
Nat Med. 2016 Apr;22(4):345-61. doi: 10.1038/nm.4071.
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Heritability of autism spectrum disorders: a meta-analysis of twin studies.自闭症谱系障碍的遗传度:双生子研究的荟萃分析
J Child Psychol Psychiatry. 2016 May;57(5):585-95. doi: 10.1111/jcpp.12499. Epub 2015 Dec 27.
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Hox genes, evo-devo, and the case of the ftz gene.同源异型基因、演化发育生物学与ftz基因实例
Chromosoma. 2016 Jun;125(3):535-51. doi: 10.1007/s00412-015-0553-6. Epub 2015 Nov 23.
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Diametrical diseases reflect evolutionary-genetic tradeoffs: Evidence from psychiatry, neurology, rheumatology, oncology and immunology.双相障碍反映了进化-遗传权衡:来自精神病学、神经病学、风湿病学、肿瘤学和免疫学的证据。
Evol Med Public Health. 2015 Sep 9;2015(1):216-53. doi: 10.1093/emph/eov021.
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Science. 2014 Dec 12;346(6215):1256846. doi: 10.1126/science.1256846.
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NMDA receptor subunit mutations in neurodevelopmental disorders.神经发育障碍中的NMDA受体亚基突变
Curr Opin Pharmacol. 2015 Feb;20:73-82. doi: 10.1016/j.coph.2014.11.008. Epub 2014 Dec 11.
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Neuromolecular responses to social challenge: common mechanisms across mouse, stickleback fish, and honey bee.对社会挑战的神经分子反应:小鼠、棘鱼和蜜蜂的共同机制
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Autism-related neuroligin-3 mutation alters social behavior and spatial learning.神经黏连蛋白 3 基因突变与自闭症相关,可改变社交行为和空间学习能力。
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