Lu‐Chen Weng

机构：Broad Institute · ORCID：0000-0003-1475-4930

发表论文 153 篇 · 总被引 12697 次 · h-index 53

代表论文

• Rare coding variant analysis for human diseases across biobanks and ancestries (2024 · Nature Genetics · 被引 60)
• Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience (2024 · Nature Genetics · 被引 55)
• Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases (2025 · Nature Genetics · 被引 51)
• Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk (2025 · Nature Genetics · 被引 30)
• The impact of common and rare genetic variants on bradyarrhythmia development (2025 · Nature Genetics · 被引 23)
• Unsupervised deep learning of electrocardiograms enables scalable human disease profiling (2025 · npj Digital Medicine · 被引 21)