STROKE英文杂志的缩写

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Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups.

Abstract:

:Background and Purpose- Mendelian stroke confers a high lifetime risk for mutation carriers; however, ethnicity-specific prevalence estimates have been difficult to establish. Methods- Eighteen genes responsible for Mendelian stroke were investigated using the Genome Aggregation Database. Genome Aggregation Database participants belonged to 1 of 7 populations: African/African-American, Latino/Admixed American, Ashkenazi Jewish, East Asian, Finnish European, non-Finnish European, and South Asian. Rare nonsynonymous variants from 101 635 participants free of neurological disease were examined for each ethnicity. Mutations were categorized according to 3 nested classes: pathogenic clinical variants, likely damaging variants based on in silico prediction, and all nonsynonymous variants. Results- ABCC6, KRIT1, CECR1, COL3A1, COL4A1, COL4A2, COLGALT1, GLA, HTRA1, NOTCH3, RNF213, and TREX1 harbored pathogenic clinical variants in Genome Aggregation Database. Across all 18 genes, total nonsynonymous carrier frequency was found to be high in 5 ethnicities (African/African-American, Latino/Admixed American, East Asian, non-Finnish European, and South Asian; 28.5%-37.5%) while lower total frequencies were estimated for in silico-predicted likely damaging variants (14.9%-19.7%) and pathogenic clinical variants (0.7%-2.8%). Overall, East Asian exhibited the highest total pathogenic clinical mutation carrier frequency (2.8%). ABCC6 pathogenic clinical variants were most prevalent among East Asian (0.8%). Pathogenic NOTCH3 variants, causal for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, were most frequent among East Asian (1.1%) and South Asian (1.2%). East Asian also demonstrated the highest carrier rate for RNF213 (0.8%). Finnish European exhibited the greatest HTRA1 frequency (0.2%), while COL4A1 pathogenic variants were most prevalent in African/African-American (0.3%). Conclusions- Especially, among pathogenic clinical variants, Mendelian stroke genetic prevalence differed significantly between populations. These prevalence estimates may serve as guides for screening and risk profiling in patients worldwide, particularly for understudied non-European populations.

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STROKE

最新影响因子：10.17	期刊ISSN：0039-2499	CiteScore：5.14
出版周期：Monthly	是否OA：YES	出版年份：1970

期刊官方网址：http://stroke.ahajournals.org/

期刊投稿地址：http://stroke-submit.aha-journals.org/cgi-bin/main.plex

自引率：9.20%	研究方向：医学-临床神经学
出版地区：UNITED STATES

SCI期刊coverage：Science Citation Index Expanded（科学引文索引扩展）

NCBI查询：PubMed Central (PMC)链接全文检索(pubmed central)

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STROKE 期刊简介

英文简介：

Stroke provides reports of clinical and basic investigation of all aspects of the cerebral circulation and its diseases from many disciplines including neurology, internal medicine, radiology, nuclear medicine, neuropathology, neurosurgery, epidemiology, vascular surgery, rehabilitation, anesthesiology, critical care medicine, vascular physiology, neuropsychology, speech pathology, and neuro-ophthalmology.

中文简介：（来自Google、百度翻译）

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STROKE 期刊中科院评价数据

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STROKE 期刊CiteScore评价数据

CiteScore排名

序号	类别	排名	百分位
1	大类(学科)：Medicine 小类(学科)：Neurology (clinical)	#17/336 点击查看排名表	94th
2	大类(学科)：Medicine 小类(学科)：Cardiology and Cardiovascular Medicine	#12/327 点击查看排名表	96th
3	大类(学科)：Nursing 小类(学科)：Advanced and Specialized Nursing	#2/50 点击查看排名表	97th

CiteScore趋势图

Scopus涵盖范围

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STROKE 期刊常见问题

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15年经验沉淀，实体公司
运营

STROKE 投稿经验

(由下方点评分析获得，16人参与，64890人阅读）

偏重的研究方向：

心脑血管 (2)
投稿录用比例：

暂无
审稿速度：

平均2.6666666666667个月的审稿周期(非官方数据)

年度总发文量	年度论文发表量	年度综述发表量
526	484	42

#2 50	STROKE	5.14	第97百分位
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Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups.