Author

Ingrid A. Harten

Benaroya Research Institute

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

Biology Disciplines

Click to filter author papers

Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:CRISPR screen· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Carl G. de BoeriD· 1 shared Daniel CampbelliD· 1 shared David R. LiuiD· 1 shared Gregory A. NewbyiD· 1 shared Hannah A. DeBergiD· 1 shared John RayiD· 1 shared Kousuke MouriiD· 1 shared Matteo GentiliiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetics

Carl G. de BoerORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Prioritization of autoimmune disease-associated genetic variants that perturb regulatory element activity in T cells

Kousuke Mouri, Michael H. Guo, Carl G. de Boer, Michelle M. Lissner, Ingrid A. Harten, Gregory A. Newby, Hannah A. DeBerg, Winona F. Platt, Matteo Gentili, David R. Liu, Daniel Campbell, Nir Hacohen, Ryan Tewhey, John Ray

The paper identifies causal genetic variants in autoimmune diseases by combining allele-specific reporter assays with chromatin accessibility data, showing their impact on gene expression and T cell function.

Nature Genetics · May 1, 2022Peer-reviewedGenetics