Genetic and clinical features of social cognition in 22q11.2 deletion syndrome
Author:
Affiliation:
1. Department of Human Neurosciences; Sapienza University; Rome 00185 Italy
2. Department of Psychosis Studies; Institute of Psychiatry, Psychology and Neuroscience, King's College; London SE5 8AF United Kingdom
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jnr.24265/fullpdf
Reference123 articles.
1. The social brain: Neural basis of social knowledge;Adolphs;Annual Review of Psychology,2009
2. Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome;Andersson;Biological Psychiatry,2008
3. Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: A 3-year follow-up study;Antshel;Journal of the American Academy of Child and Adolescent Psychiatry,2010
4. Efficacy of community treatments for schizophrenia and other psychotic disorders: A literature review;Armijo;Frontiers in Psychiatry,2013
5. Phenotypic characterization of cognition and social behavior in mice with heterozygous versus homozygous deletion of catechol-O-methyltransferase;Babovic;Neuroscience,2008
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Increased burden of rare protein‐truncating variants in constrained, brain‐specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder;Genes, Brain and Behavior;2024-02
2. The Impact of Genetics on Cognition: Insights into Cognitive Disorders and Single Nucleotide Polymorphisms;Journal of Personalized Medicine;2024-01-30
3. Social cognition and real‐life functioning in patient samples with 22q11.2 deletion syndrome with or without psychosis, compared to a large sample of patients with schizophrenia only and healthy controls;Journal of Neuropsychology;2023-05-09
4. The Relationship between Motor Symptoms, Signs, and Parkinsonism with Facial Emotion Recognition Deficits in Individuals with 22q11.2 Deletion Syndrome at High Genetic Risk for Psychosis;Acta Neurologica Scandinavica;2023-03-28
5. Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia;Archives of Medical Research;2022-06
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3