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Themistocles L. Assimes

va palo alto health care system
H指数:99
被引数:6.9万

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Ancestry-specific DNA methylation signatures of smoking and associations with atherosclerotic cardiovascular disease risk: findings from the Million Veteran Program

吸烟的祖先特异性DNA甲基化特征及其与动脉粥样硬化性心血管疾病风险的关系:百万军人计划的研究结果

2026-09-100
OA
Linkage disequilibrium and allelic heterogeneity explain variation in coronary artery disease risk at 9p21 across populations and reduced effect in Africans

连锁不平衡和等位基因异质性解释了9p21位点多个人群中冠状动脉疾病风险的差异以及非洲人群中的减弱效应

2026-07-010
PRE
Exome-wide association study of blood lipids in 1,158,017 individuals from diverse populations

不同人群1,158,017个体血脂的全外显子组关联研究

2026-05-250
OAAI
Causal relationship between epigenetic markers and type 2 diabetes in West African populations: a Mendelian randomisation analysis

西非人群中表观遗传标记与2型糖尿病的因果关系:一项孟德尔随机化分析

2026-04-240
OAAI
Simulated patient systems powered by large language model-based AI agents offer potential for transforming medical education

基于大型语言模型AI代理的模拟病人系统为医学教育转型提供了潜力

2025-12-190
OAAI
Polygenic risk score for type 2 diabetes shows context-dependent effects across populations

2型糖尿病的多基因风险评分在人群中显示出依赖情境的影响

2025-10-010
OAAI
Systems Age: a single blood methylation test to quantify aging heterogeneity across 11 physiological systems

系统时代:一种单次血液甲基化检测方法,用于量化11个生理系统中的衰老异质性

2025-09-150
PRE
CYP2C19 Polymorphisms and Clinical Outcomes Following Percutaneous Coronary Intervention in the Million Veteran Program

CYP2C19多态性与经皮冠状动脉介入治疗后百万退伍军人计划中的临床结局

2025-06-030
OAAI
Bidirectional associations of zinc supplement intake with biological ageing interacted by metabolic equivalent of task: A large-scale population-based Biobank study

锌补充剂摄入与生物衰老的双向关联:受代谢当量调节的大规模人群生物银行研究

2025-05-020
OA
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

罕见的有害CCR2变异与较低的生命周期心血管风险相关

2025-03-211
OA
Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height

基于遗传预测身高所得的最大异质性祖先别特异性疾病图谱的见解

2025-02-270
OA
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants

通过常见和罕见的结构变异揭示冠状动脉疾病的遗传景观

2025-02-181
OAAI
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

全基因组关联分析确定不同祖先年龄相关性黄斑变性的不同遗传结构

2024-12-020
PRE
Associations of blood lipids and LDL cholesterol lowering drug-targets with colorectal cancer risk: a Mendelian randomisation study
2024-11-230
OA
Exome-wide association study of over a million individuals identified effector genes and variants for blood lipids

全外显子组关联研究对超过一百万个体进行了分析,确定了与血脂相关的效应基因和变异。

2024-11-120
PRE
Variant-enhancer-gene mapping at the 9p21 locus in smooth muscle cells reveals new enhancer-gene pairs and mechanistic insights for coronary artery disease

在平滑肌细胞中9p21位点的变异增强子-基因作图揭示了新的增强子-基因对以及对冠状动脉疾病机制的见解

2024-11-120
PRE