Patricia A. Peyser

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun, Daniel Harris, Michael D. Kessler et al. · Nature · 2021 · 2.2K citations · Full text

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Anubha Mahajan, Daniel Taliun, Matthias Thurner et al. · Nature Genetics · 2018 · 1.9K citations · Full text

Genome-wide Association Study, Allelic Variant, Genetic Determinant +11

A saturated map of common genetic variants associated with human height

Loïc Yengo, Sailaja Vedantam, Eirini Marouli et al. · Nature · 2022 · 827 citations · Full text

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Alexander G. Bick, Joshua S. Weinstock, Satish K. Nandakumar et al. · Nature · 2020 · 698 citations · Full text

Genetic Disorder, Genetics, Hematology +3

A Null Mutation in Human <i>APOC3</i> Confers a Favorable Plasma Lipid Profile and Apparent Cardioprotection

Toni I. Pollin, Coleen Damcott, Haiqing Shen et al. · Science · 2008 · 675 citations · Full text