Author

Heather R. Flanagan‐Steet

Greenwood Genetic CenterORCID 0000-0001-8295-0453Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:zebrafish· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:protein structure· 1

Frequent Co-Authors

David B. EvermaniD· 2 shared Brittany T. Truong· 1 shared Charles E. SchwartziD· 1 shared Chelsi Jeter· 1 shared Cindy D. SkinneriD· 1 shared Cynthia J. TifftiD· 1 shared David M. VirshupiD· 1 shared David R. AdamsiD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

David B. EvermanORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineDisease Models & MechanismsPeer-reviewedApr 1, 2023

PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in Split Hand/Foot Malformation

Brittany T. Truong, Lomeli Carpio Shull, Ezra S. Lencer…·Kristin Artinger

The paper identifies PRDM1 variants causing Split Hand/Foot Malformation and shows their functional impact on limb development through zebrafish experiments and gene expression analysis.

10 citations

zebrafishwhole-exome sequencing

𝕏 PostBluesky

Molecular BiologyJournal of Cell SciencePeer-reviewedNov 24, 2021

Structural model of PORCN illuminates disease-associated variants and drug binding sites

Jia Yu, Pei-Ju Liao, Weijun Xu…·David M. Virshup

The paper develops a structural model of PORCN, revealing its catalytic mechanism, disease-associated variants, and drug binding sites.

29 citations

humanprotein structure

𝕏 PostBluesky

Developmental BiologyDisease Models & MechanismsPeer-reviewedJan 1, 2020

Deficiency in the endocytic adaptor protein PHETA1/2 impairs renal and craniofacial development

Kristin M. Ates, Tong Wang, Trevor Moreland…·Y. Albert Pan

This study investigates the role of PHETA1/2 in zebrafish, showing that their deficiency causes renal and craniofacial defects, and links a patient variant to disease pathogenesis.

9 citations

zebrafishexperimental assay

𝕏 PostBluesky