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Age-specific heterogeneity of genetic susceptibility to cardiovascular disease might have opposite outcomes depending on the presence of prediabetes
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作者 chaeyoung lee 《World Journal of Diabetes》 SCIE 2024年第6期1381-1383,共3页
Examining age-specific heterogeneity of susceptibility to cardiovascular disease is also essential in individuals without prediabetes to determine its relative size and direction compared to those with prediabetes.Of ... Examining age-specific heterogeneity of susceptibility to cardiovascular disease is also essential in individuals without prediabetes to determine its relative size and direction compared to those with prediabetes.Of particular interest,age-specific heterogeneity in genetic susceptibility may exhibit opposite directions depending on the presence or absence of prediabetes. 展开更多
关键词 Age-specific difference Cardiovascular disease Genetic heterogeneity by age Genetic susceptibility PREDIABETES
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Heterogeneous genetic architecture by gender for precision medicine of cardiovascular disease
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作者 chaeyoung lee 《Journal of Geriatric Cardiology》 SCIE CAS CSCD 2018年第5期325-327,共3页
It is well-known that gender differences exist in the onset, progression, and prognosis of cardiovascular diseases (CVDs), and that risk factors such as high blood pressure and lipid profiles vary between men and wo... It is well-known that gender differences exist in the onset, progression, and prognosis of cardiovascular diseases (CVDs), and that risk factors such as high blood pressure and lipid profiles vary between men and women, Cur- rently, sex differences are stressed as important variables to take into account when examining the etiology of CVD. Genome-wide association studies of CVD have employed the sex as a covariate in their analytical models, but generally disregarded potential genetic heterogeneity (GHS) attributable to sex. 展开更多
关键词 Cardiovascular disease Genetic heterogeneity Genome-wide association study Mixed model Sex difference
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国际卒中遗传学联盟的推荐意见(第1部分):标准化表型数据收集 被引量:3
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作者 Jennifer J. Majersik John W.Cole +25 位作者 Jonathan Golledge Natalia S. Rost Yu-Feng Yvonne Chan M. Edip Gurol Ame G. Lindgren Daniel Woo Israel Fernandez-Cadenas Donna T. Chen Vincent Thijs Bradford B. Worrall Ayeesha Kamal Paul Bentley Joanna M. Wardlaw Ynte M. Ruigrok Thomas W.K Battey Reinhold Schmidt Joan Montaner Anne-Katrin Giese Jaume Roquer Jordi Jimenez-Conde chaeyoung lee Hakan Ay Juan Jose Martin 李海峰 岳耀先 徐军 《国际脑血管病杂志》 2015年第9期645-650,共6页
与几乎所有复杂疾病一样,卒中的患病风险和临床转归也是多基因作用的[1]。探索相关基因突变有望为新型个体化治疗方法奠定基础,从而显著减少卒中对全球健康造成的毁灭性影响。为了达到足够的统计学效能以确认多个风险性等位基因,需要很... 与几乎所有复杂疾病一样,卒中的患病风险和临床转归也是多基因作用的[1]。探索相关基因突变有望为新型个体化治疗方法奠定基础,从而显著减少卒中对全球健康造成的毁灭性影响。为了达到足够的统计学效能以确认多个风险性等位基因,需要很大的样本量。尽管卒中是全世界范围内第二大致死病因和成年人致残的主要原因[2],但没有任何一家研究机构能独立收集到足够的样本。在认识到这一挑战之后,来自世界各地的卒中研究者们于2007年成立了国际卒中遗传学联盟( International Stroke Genetics Consortium, ISGC; http://www. strokegenetics.org),其使命是通过研究在全球多个研究机构入组的患者来识别影响卒中患病风险、临床预后和治疗效果的遗传学因素。尽管先前已取得了一些成功[3-5],仍有大量工作有待进行,这不仅是为了发现风险性等位基因从而达到卒中个体化医疗的最终目标,更是为了开发综合性卒中风险评估手段以及得到足以改变临床实践的结果[6]。根据糖尿病和冠状动脉疾病等其他复杂疾病的研究进展,为了识别与卒中相关的所有基因突变,需要100000~200000个样本。为了达到这个样本量,需要进行更为广泛的协作。 展开更多
关键词 遗传学因素 数据收集 卒中 国际 标准化 个体化医疗 表型 冠状动脉疾病
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国际卒中遗传学联盟的推荐意见(第2部分):生物样本的采集和储存 被引量:2
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作者 Thomas W.K.Battey Valerie Valant +21 位作者 Sylvia Baedorf Kassis Christina Kourkoulis chaeyoung lee Christopher D. Anderson Guido J. Falcone Jordi Jimenez-Conde Israel Fernandez-Cadenas Guillaume Pare Tatjana Rundek Michael L. James Robin Lemmens Tsong-Hai lee Turgut Tatlisumak Steven J. Kittner Arne Lindgren Farrah J. Mateen Aaron L. Berkowitz Elizabeth G. Holliday Jennifer Majersik 李海峰 姜平 岳耀先 《国际脑血管病杂志》 2015年第9期651-656,共6页
在2003年人类基因组测序以及全基因组基因分型技术发展的共同促进下,人类遗传学的进步已使我们识别出2000多个与性状相关的基因突变。由于这些突变大多数对疾病风险仅有微小的独立影响,因此成功的遗传学研究需要很大的样本量(包含数... 在2003年人类基因组测序以及全基因组基因分型技术发展的共同促进下,人类遗传学的进步已使我们识别出2000多个与性状相关的基因突变。由于这些突变大多数对疾病风险仅有微小的独立影响,因此成功的遗传学研究需要很大的样本量(包含数以千计、万计或者十万计的病例和对照)才能达到足够的研究效能。如此大的样本量积累需要依赖在人类遗传学研究乃至在临床研究中史无前例的大规模国际协作。现在已有许多常见疾病的专病联盟将大量独立机构和合作者联合起来。每个联盟均面临至少2个基本问题:如何整合具有足够数量、同质性和表型质量高的研究样本以及如何储存和分析来自入组受试者的生物样本,有时可能需要在数年间反复进行。 展开更多
关键词 人类遗传学 生物样本 国际协作 储存 人类基因组测序 采集 卒中 基因分型技术
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On the Evolutionary Dynamics of the Cahn-Hilliard Equation with Cut-Off Mass Source
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作者 chaeyoung lee Hyundong Kim +4 位作者 Sungha Yoon Jintae Park Sangkwon Kim Junxiang Yang Junseok Kim 《Numerical Mathematics(Theory,Methods and Applications)》 SCIE CSCD 2021年第1期242-260,共19页
We investigate the effect of cut-off logistic source on evolutionary dynamics of a generalized Cahn-Hilliard(CH)equation in this paper.It is a well-known fact that the maximum principle does not hold for the CH equati... We investigate the effect of cut-off logistic source on evolutionary dynamics of a generalized Cahn-Hilliard(CH)equation in this paper.It is a well-known fact that the maximum principle does not hold for the CH equation.Therefore,a generalized CH equation with logistic source may cause the negative concentration blow-up problem in finite time.To overcome this drawback,we propose the cut-off logistic source such that only the positive value greater than a given critical concentration can grow.We consider the temporal profiles of numerical results in the one-,two-,and three-dimensional spaces to examine the effect of extra mass source.Numerical solutions are obtained using a finite difference multigrid solver.Moreover,we perform numerical tests for tumor growth simulation,which is a typical application of generalized CH equations in biology.We apply the proposed cut-off logistic source term and have good results. 展开更多
关键词 Cahn-Hilliard equation logistic source finite difference method tumor growth application
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