Analysis ofCHRNA7rare variants in autism spectrum disorder susceptibility

Author:

Bacchelli Elena1,Battaglia Agatino2,Cameli Cinzia1,Lomartire Silvia1,Tancredi Raffaella2,Thomson Susanne3,Sutcliffe James S3,Maestrini Elena1

Affiliation:

1. Department of Pharmacy and Biotechnology; University of Bologna; Bologna Italy

2. Stella Maris Clinical Research Institute for Child and Adolescent Neuropsychiatry; Calambrone (Pisa) Italy

3. Department of Molecular Physiology & Biophysics and Psychiatry and Vanderbilt Brain Institute; Vanderbilt University; Nashville Tennessee

Funder

University of Bologna

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference41 articles.

1. Mammalian nicotinic acetylcholine receptors: from structure to function;Albuquerque;Physiol Rev,2009

2. Role of Kenae/CCDC125 in cell motility through the deregulation of RhoGTPase;Araya;Int J Mol Med,2009

3. Microdeletion 15q13.3: A locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders;Ben-Shachar;J Med Genet,2009

4. Synaptic plasticity and the neurobiology of learning and memory;Benfenati;Acta Biomed,2007

5. Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci;Chilian;Clin Genet,2013

Cited by 45 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

同舟云学术

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