Author

Laura M Raffield

University of North Carolina School of Medicine;

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Assay:electronic health records· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

David N Cooper· 1 shared David Stein· 1 shared Hanna Abe· 1 shared Jerome I Rotter· 1 shared Leslie A Lange· 1 shared Mark O Goodarzi· 1 shared Meltem Ece KarsiD· 1 shared Michael Tsai· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

David N Cooper

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 13, 2026

The phenomic landscape of rare gain- and loss-of-function variation

Meltem Ece Kars, David Stein, Yiming Wu…·Yuval Itan

This study examines rare gain- and loss-of-function variants across 18,214 genes using whole-exome sequencing and electronic health records to identify ancestry-specific and shared gene-variant associations with various traits.

DOI 10.64898/2026.11.11.26367788

humanwhole-exome sequencing

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