Daniel Harris

机构：California University of Pennsylvania, University of Pennsylvania · ORCID：0000-0001-8150-6000

发表论文 46 篇 · 总被引 6673 次 · h-index 26

代表论文

• Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022 · Nature Genetics · 被引 370)
• Clonal haematopoiesis and risk of chronic liver disease (2023 · Nature · 被引 216)
• A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (2021 · Nature Genetics · 被引 198)
• A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies (2022 · Nature Methods · 被引 115)
• Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis (2023 · Nature · 被引 109)
• Whole genome sequence analysis of blood lipid levels in >66,000 individuals (2022 · Nature Communications · 被引 76)