Laura M. Raffield
University of North Carolina at Chapel Hill(US)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Genomics and Rare Diseases, RNA modifications and cancer, Cancer Genomics and Diagnostics
Most-Cited Works
- → The trans-ancestral genomic architecture of glycemic traits(2021)870 cited
- → The Polygenic and Monogenic Basis of Blood Traits and Diseases(2020)719 cited
- → Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations(2020)712 cited
- → Inherited causes of clonal haematopoiesis in 97,691 whole genomes(2020)709 cited
- → Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation(2022)705 cited
- → Genetic drivers of heterogeneity in type 2 diabetes pathophysiology(2024)445 cited
- → Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data(2022)348 cited
- → Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations(2019)317 cited
- → Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging(2021)290 cited
- → Association of Clonal Hematopoiesis With Incident Heart Failure(2021)205 cited