Next generation sequencing for neurological diseases: New hope or new hype?
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Surgery
Reference52 articles.
1. Risk alleles for multiple sclerosis identified by a genomewide study;Hafler;New England Journal of Medicine,2007
2. Genome-wide association study of severity in multiple sclerosis. Genes and Immunity 2011;12(8):615–25.
3. Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population;Liu;BMC Medical Genetics,2011
4. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease;Polymeropoulos;Science,1997
5. Mutations in the parkin gene cause autosomal recessive Juvenile Parkinsonism;Kitada;Nature,1998
Cited by 21 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. Next-generation sequencing and bioinformatics in rare movement disorders;Nature Reviews Neurology;2024-01-03
2. Neurogenomics in Africa: current state, challenges, opportunities, and recommendation;Annals of Medicine & Surgery;2023-02
3. Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s Disease;Frontiers in Genetics;2022-03-01
4. Genetic testing in neurology: What every neurologist must know;Annals of Indian Academy of Neurology;2022
5. Molecular and Genetic Therapies;Neuromuscular Disorders;2022
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