缺血性脑卒中病因学亚型的遗传学分析

[1] 进展性缺血性脑卒中患者血IL-6、TNF-α、S-100b蛋白水平的变化及临床意义 [J]. 疑难病杂志, 2007, (11) : 658 - 661

[2] 5,10-亚甲基四氢叶酸还原酶基因C677T突变与再发脑梗死的关系 [J]. 卒中与神经疾病, 2007, (01) : 10 - 12

[3] 载脂蛋白E基因多态性及脂类代谢与缺血性脑卒中亚型关系的研究 [J]. 中华老年心脑血管病杂志, 2006, (08) : 513 - 516

[4] N,N-亚甲基四氢叶酸还原酶基因与缺血性脑卒中发病的关系 [J]. 中国危重病急救医学, 2006, (05) : 264 - 267

[5] Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke: A Large-Scale Genetic Association Study[J] . Circulation: Cardiovascular Genetics . 2009 (2)

[6] A Meta-Analysis of Candidate Gene Polymorphisms and Ischemic Stroke in 6 Study Populations: Association of Lymphotoxin-Alpha in Nonhypertensive Patients[J] . Xingyu Wang,Suzanne Cheng,Victoria H. Brophy,Henry A. Erlich,Christine Mannhalter,Klaus Berger,Wolfgang Lalouschek,Warren S. Browner,Yu Shi,E Bernd Ringelstein,Christof Kessler,Jan Luedemann,Klaus Lindpaintner,Lisheng Liu,Paul M. Ridker,Robert Y.L. Zee,Nancy R. Cook.Stroke . 2009 (3)

[7] Decoding Cryptogenic Cardioembolism [J]. ANNALS OF NEUROLOGY, 2008, 64 (04) : 364 - 366

[8] Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21 [J]. STROKE, 2008, 39 (05) : 1586 - 1589

[9] Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease[J] . Circulation . 2008 (13)

[10] A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release[J] . Mar Matarín,W Mark Brown,Sonja Scholz,Javier Simón-Sánchez,Hon-Chung Fung,Dena Hernandez,J Raphael Gibbs,Fabienne Wavrant De Vrieze,Cynthia Crews,Angela Britton,Carl D Langefeld,Thomas G Brott,Robert D Brown,Bradford B Worrall,Michael Frankel,Scott Silliman,L Douglas Case,Andrew Singleton,John A Hardy,Stephen S Rich,James F Meschia.Lancet Neurology . 2007 (5)

[1] 进展性缺血性脑卒中患者血IL-6、TNF-α、S-100b蛋白水平的变化及临床意义 [J]. 疑难病杂志, 2007, (11) : 658 - 661

[2] 5,10-亚甲基四氢叶酸还原酶基因C677T突变与再发脑梗死的关系 [J]. 卒中与神经疾病, 2007, (01) : 10 - 12

[3] 载脂蛋白E基因多态性及脂类代谢与缺血性脑卒中亚型关系的研究 [J]. 中华老年心脑血管病杂志, 2006, (08) : 513 - 516

[4] N,N-亚甲基四氢叶酸还原酶基因与缺血性脑卒中发病的关系 [J]. 中国危重病急救医学, 2006, (05) : 264 - 267

[5] Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke: A Large-Scale Genetic Association Study[J] . Circulation: Cardiovascular Genetics . 2009 (2)

[6] A Meta-Analysis of Candidate Gene Polymorphisms and Ischemic Stroke in 6 Study Populations: Association of Lymphotoxin-Alpha in Nonhypertensive Patients[J] . Xingyu Wang,Suzanne Cheng,Victoria H. Brophy,Henry A. Erlich,Christine Mannhalter,Klaus Berger,Wolfgang Lalouschek,Warren S. Browner,Yu Shi,E Bernd Ringelstein,Christof Kessler,Jan Luedemann,Klaus Lindpaintner,Lisheng Liu,Paul M. Ridker,Robert Y.L. Zee,Nancy R. Cook.Stroke . 2009 (3)

[7] Decoding Cryptogenic Cardioembolism [J]. ANNALS OF NEUROLOGY, 2008, 64 (04) : 364 - 366

[8] Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21 [J]. STROKE, 2008, 39 (05) : 1586 - 1589

[9] Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease[J] . Circulation . 2008 (13)

[10] A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release[J] . Mar Matarín,W Mark Brown,Sonja Scholz,Javier Simón-Sánchez,Hon-Chung Fung,Dena Hernandez,J Raphael Gibbs,Fabienne Wavrant De Vrieze,Cynthia Crews,Angela Britton,Carl D Langefeld,Thomas G Brott,Robert D Brown,Bradford B Worrall,Michael Frankel,Scott Silliman,L Douglas Case,Andrew Singleton,John A Hardy,Stephen S Rich,James F Meschia.Lancet Neurology . 2007 (5)