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I

Iftikhar J. Kullo

Mayo Clinic
H指数:83
被引数:2.5万

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Recommendations for return of secondary genomic findings in observational cohort studies

观察性队列研究中二次基因组学发现反馈的建议

2026-09-110
PRE
A pre-train and fine-tune framework for adaptive boosting of pre-trained polygenic risk scores

预训练和多任务微调框架用于自适应提升预训练多基因风险评分

2026-08-290
OAAI
Additive value of polygenic risk and family history for coronary heart disease risk stratification in two diverse US cohorts

多基因风险评分与家族史对冠状动脉心脏病风险分层在两个不同美国队列中的附加价值

2026-08-010
PRE
Coronary Artery Disease Polygenic Risk Score and Recurrent Cardiovascular Events After Coronary Artery Revascularization: A UK Biobank Analysis

冠状动脉疾病多基因风险评分与冠状动脉血管重建后心血管事件复发:一项英国生物银行分析

2026-07-250
OAAI
Healthcare professionals’ experiences returning monogenic, polygenic, and integrated risk results in the eMERGE study

医疗专业人员返馈单基因、多基因和综合风险结果在eMERGE研究中的经验

2025-12-060
OAAI
Author Correction: Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

作者更正:心力衰竭在等位基因频率谱中的常见变异和罕见变异遗传结构

2025-11-280
PRE
Recommendations for responsible use of population descriptors in polygenic risk score development

关于在多基因风险评分开发中负责任使用人群描述符的建议

2025-11-240
PRE
Recognition and management of persistent chylomicronemia: A joint expert clinical consensus by the National Lipid Association and the American Society for Preventive Cardiology

持续性乳糜微粒血症的识别和管理: 国家脂质协会和美国预防心脏病学协会的联合专家临床共识

2025-06-010
OAAI
Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementation

为eMERGE Network参与者的医疗保健费用提供覆盖:公平性与实施方面的挑战

2025-05-160
PRE
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

心衰在等位基因频率谱上的常见变异和罕见变异遗传结构

2025-04-070
PRE
Recognition and management of persistent chylomicronemia: A Joint Expert Clinical Consensus by the National Lipid Association and the American Society for Preventive Cardiology

持久性乳糜微粒血症的识别与管理:国家脂质协会与美国预防心脏病学会联合专家临床共识

2025-03-280
OAAI
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
The PRIMED Consortium: Reducing disparities in polygenic risk assessment

PRIMED联盟: 减少多基因风险评估中的差异

2024-12-011
OAAI