Neuropathology of 16p13.11 Deletion in Epilepsy
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference49 articles.
1. Origins and functional impact of copy number variation in the human genome.;DF Conrad;Nature,2010
2. High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.;TH Shaikh;Genome Res,2009
3. A genome-wide investigation of SNPs and CNVs in schizophrenia.;AC Need;PLoS Genet,2009
4. Recurrent reciprocal deletions and duplications of 16p13.11: The deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.;FD Hannes;J Med Genet,2009
5. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.;R Ullmann;Hum Mutat,2007
Cited by 18 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. Cytogenomic epileptology;Molecular Cytogenetics;2023-01-05
2. 16p13.11 deletion variants associated with neuropsychiatric disorders cause morphological and synaptic changes in induced pluripotent stem cell-derived neurons;Frontiers in Psychiatry;2022-11-03
3. Epilepsy Surgery: Special Circumstances;Seminars in Pediatric Neurology;2021-10
4. Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: Clues into the underlying mechanisms leading to disease;Seizure;2021-08
5. Duplication of chromosome 16p13.11-p12.3 with different expressions in the same family;Balkan Journal of Medical Genetics;2021-06-01
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