Stroke genome-wide association studies: the large numbers imperative.
作者信息
Meschia James F
出版信息
Stroke. 2010 Apr;41(4):579-80. doi: 10.1161/STROKEAHA.109.576769. Epub 2010 Feb 25.
Abstract
摘要
相似文献
1
Stroke genome-wide association studies: the large numbers imperative.中风全基因组关联研究：大量样本的必要性。
Stroke. 2010 Apr;41(4):579-80. doi: 10.1161/STROKEAHA.109.576769. Epub 2010 Feb 25.
2
ε4 is associated with younger age at ischemic stroke onset but not with stroke outcome.ε4与缺血性卒中发病时较年轻的年龄相关，但与卒中结局无关。
Neurology. 2019 Nov 5;93(19):849-853. doi: 10.1212/WNL.0000000000008459. Epub 2019 Oct 16.
3
Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke.影响凝血因子XIII B亚基的遗传因素与缺血性中风风险相关。
Stroke. 2015 Aug;46(8):2069-74. doi: 10.1161/STROKEAHA.115.009387. Epub 2015 Jul 9.
4
Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies.多基因遗传风险评分与病例对照和前瞻性队列研究中的缺血性卒中相关。
Stroke. 2014 Feb;45(2):394-402. doi: 10.1161/STROKEAHA.113.002938. Epub 2014 Jan 16.
5
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.全基因组关联研究的荟萃分析确定了非裔美国人中风的遗传风险因素。
Stroke. 2015 Aug;46(8):2063-8. doi: 10.1161/STROKEAHA.115.009044. Epub 2015 Jun 18.
6
Genome-Wide Polygenic Score and the Risk of Ischemic Stroke in a Prospective Cohort: The Hisayama Study.全基因组多基因风险评分与前瞻性队列中缺血性卒中的风险：日山研究。
Stroke. 2020 Mar;51(3):759-765. doi: 10.1161/STROKEAHA.119.027520. Epub 2020 Jan 31.
7
Genetic Risk Factors for Ischemic and Hemorrhagic Stroke.缺血性和出血性中风的遗传风险因素
Curr Cardiol Rep. 2016 Dec;18(12):124. doi: 10.1007/s11886-016-0804-z.
8
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.缺血性中风与 ABO 基因座相关：EuroCLOT 研究。
Ann Neurol. 2013 Jan;73(1):16-31. doi: 10.1002/ana.23838.
9
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke.全基因组关联研究荟萃分析 22000 名非裔个体的中风，鉴定出与中风相关的新关联。
Stroke. 2020 Aug;51(8):2454-2463. doi: 10.1161/STROKEAHA.120.029123. Epub 2020 Jul 22.
10
Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.缺血性卒中的低频和常见基因变异：METASTROKE合作研究
Neurology. 2016 Mar 29;86(13):1217-26. doi: 10.1212/WNL.0000000000002528. Epub 2016 Mar 2.
引用本文的文献
1
Emerging insights from the genetics of cerebral small-vessel disease.脑小血管病遗传学的新见解。
Ann N Y Acad Sci. 2020 Jul;1471(1):5-17. doi: 10.1111/nyas.13998. Epub 2019 Jan 8.
2
Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.探寻脑静脉血栓形成的遗传基础——BEAST研究联盟：一项研究方案
BMJ Open. 2016 Nov 22;6(11):e012351. doi: 10.1136/bmjopen-2016-012351.
3
Stroke genomics in people of African ancestry: charting new paths.非洲裔人群的中风基因组学：开辟新道路。
Cardiovasc J Afr. 2015 Mar-Apr;26(2 Suppl 1):S39-49. doi: 10.5830/CVJA-2015-039.
4
Genetics studies in ischaemic stroke.缺血性脑卒中的遗传学研究。
Transl Stroke Res. 2010 Dec;1(4):238-45. doi: 10.1007/s12975-010-0041-5. Epub 2010 Aug 31.
5
Clinical neurogenetics: stroke.临床神经遗传学：中风。
Neurol Clin. 2013 Nov;31(4):915-28. doi: 10.1016/j.ncl.2013.05.001. Epub 2013 Jul 17.
6
Exploring the interaction between SNP genotype and postmenopausal hormone therapy effects on stroke risk.探讨 SNP 基因型与绝经后激素治疗对卒中风险的交互作用。
Genome Med. 2012 Jul 13;4(7):57. doi: 10.1186/gm358. eCollection 2012.
7
Drug resistance in epilepsy and the ABCB1 gene: The clinical perspective.癫痫中的耐药性与ABCB1基因：临床视角
Indian J Hum Genet. 2011 May;17 Suppl 1(Suppl 1):S12-21. doi: 10.4103/0971-6866.80353.
本文引用的文献
1
Advances in genomic analysis of stroke: what have we learned and where are we headed?中风的基因组分析进展：我们学到了什么，我们的方向在哪里？
Stroke. 2010 Apr;41(4):825-32. doi: 10.1161/STROKEAHA.109.570523. Epub 2010 Feb 18.
2
Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse.遗传关联研究的荟萃分析：方法学、研究间异质性和赢家的诅咒。
J Hum Genet. 2009 Nov;54(11):615-23. doi: 10.1038/jhg.2009.95. Epub 2009 Oct 23.
3
Meta-analysis of genome-wide association studies: no efficiency gain in using individual participant data.全基因组关联研究的荟萃分析：使用个体参与者数据没有效率增益。
Genet Epidemiol. 2010 Jan;34(1):60-6. doi: 10.1002/gepi.20435.
4
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.在欧洲血统个体中，ZFHX3基因的变异与心房颤动有关。
Nat Genet. 2009 Aug;41(8):879-81. doi: 10.1038/ng.416. Epub 2009 Jul 13.
5
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases.全基因组关联研究、领域概述以及关于遗传变异与人类疾病知识库的发展。
Am J Epidemiol. 2009 Aug 1;170(3):269-79. doi: 10.1093/aje/kwp119. Epub 2009 Jun 4.
6
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.9号染色体短臂21.3区域的序列变异会增加动脉粥样硬化性中风的风险。
Ann Neurol. 2009 May;65(5):531-9. doi: 10.1002/ana.21590.
7
Genomewide association studies of stroke.中风的全基因组关联研究。
N Engl J Med. 2009 Apr 23;360(17):1718-28. doi: 10.1056/NEJMoa0900094. Epub 2009 Apr 15.
8
Meta-analysis in genome-wide association studies.全基因组关联研究中的荟萃分析。
Pharmacogenomics. 2009 Feb;10(2):191-201. doi: 10.2217/14622416.10.2.191.
9
Impact of restricting enrollment in stroke genetics research to adults able to provide informed consent.将中风遗传学研究的招募对象限制为能够提供知情同意书的成年人的影响。
Stroke. 2008 Mar;39(3):831-7. doi: 10.1161/STROKEAHA.107.494518. Epub 2008 Feb 7.
10
A computerized algorithm for etiologic classification of ischemic stroke: the Causative Classification of Stroke System.一种用于缺血性卒中病因分类的计算机算法：卒中病因分类系统
Stroke. 2007 Nov;38(11):2979-84. doi: 10.1161/STROKEAHA.107.490896. Epub 2007 Sep 27.
Zotero 插件