Literature DB >> 11339244

Advances in the genetics of cerebrovascular disease and stroke.

G J Hademenos1, M J Alberts, I Awad, M Mayberg, T Shepard, A Jagoda, R E Latchaw, H W Todd, K Viste, R Starke, M S Girgus, J Marler, M Emr, N Hart.   

Abstract

MEDLINE searches identified epidemiologic, experimental, and clinical studies on the genetics of cerebrovascular disease and stroke, including the following topics: genetic epidemiology of stroke; genetics of systemic disorders that cause ischemic stroke, including coagulation disorders, connective tissue disorders, vasculopathies, metabolic disorders, and disorders of unknown etiology; and genetics of systemic disorders that cause hemorrhagic stroke. Recent discoveries in stroke genetics involve the genetic basis of monogenic disorders such as cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and sickle cell disease. Reproducing similar advances in other forms of cerebrovascular disease and stroke will be more difficult because their inheritance is complex, multigenic, and heterogeneous. However, the future is promising with the application of molecular genetic approaches such as linkage analysis, allele-sharing methods, association studies, and polygenic analysis of experimental crosses as well as the transmission/disequilibrium test--a statistical method for detection of linkage between a marker and a disease-susceptibility locus.

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Year:  2001        PMID: 11339244     DOI: 10.1212/wnl.56.8.997

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  9 in total

1.  Potential association between frequent nonsynonymous variant of NPPA and cardioembolic stroke.

Authors:  Jeong-Hyun Kim; Bo-Hyung Jang; Ho Yeon Go; Sunju Park; Yong-Cheol Shin; Sung-Hoon Kim; Seong-Gyu Ko
Journal:  DNA Cell Biol       Date:  2012-03-08       Impact factor: 3.311

2.  Impact of genetic testing on complex diseases.

Authors:  M J E van Rijn; C M van Duijn; A J C Slooter
Journal:  Eur J Epidemiol       Date:  2005       Impact factor: 8.082

Review 3.  The genetics of intracranial aneurysms.

Authors:  Boris Krischek; Ituro Inoue
Journal:  J Hum Genet       Date:  2006-05-31       Impact factor: 3.172

4.  Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Authors:  A Driss; K O Asare; J M Hibbert; B E Gee; T V Adamkiewicz; J K Stiles
Journal:  Genomics Insights       Date:  2009-07-30

5.  Association Between Paraoxonase Gene Polymorphisms and Intracerebral Hemorrhage in a Korean Population.

Authors:  Hae Jeong Park; Su Kang Kim; Hyun-Kyung Park; Joo-Ho Chung
Journal:  J Mol Neurosci       Date:  2015-07-31       Impact factor: 3.444

Review 6.  Familial inflammatory Sneddon's syndrome-case report and review of the literature.

Authors:  M Szmyrka-Kaczmarek; T Daikeler; D Benz; I Koetter
Journal:  Clin Rheumatol       Date:  2004-08-31       Impact factor: 2.980

7.  Association between Val/Leu(247) polymorphism of apolipoprotein H and cerebral infarction in a Chinese population.

Authors:  Jian Xia; Mei Yuan; Hong-wei Xu; Le Zhang; Xiao-ping Du; Yun-hai Liu; Qi-dong Yang
Journal:  J Thromb Thrombolysis       Date:  2008-09-07       Impact factor: 2.300

8.  Risk of cerebral arteriovenous malformation rupture during pregnancy and puerperium.

Authors:  Xing-ju Liu; Shuo Wang; Yuan-li Zhao; Mario Teo; Peng Guo; Dong Zhang; Rong Wang; Yong Cao; Xun Ye; Shuai Kang; Ji-Zong Zhao
Journal:  Neurology       Date:  2014-04-23       Impact factor: 9.910

Review 9.  Sneddon's syndrome: a comprehensive review of the literature.

Authors:  Shengjun Wu; Ziqi Xu; Hui Liang
Journal:  Orphanet J Rare Dis       Date:  2014-12-31       Impact factor: 4.123

  9 in total

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