Author

Lisa Stout

Washington University in St. Louis

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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Developmental Biology· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:mouse· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Jeannine M. BastaiD· 2 shared Lynn RobbinsiD· 2 shared Michael I. RauchmaniD· 2 shared Michelle BrennaniD· 2 shared Samir V. ParikhiD· 2 shared Afolarin Amodu· 1 shared Alexander MoralesiD· 1 shared Amanda L. KnoteniD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersMolecular Biology

Jeannine M. BastaORCID

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Author profile →

3 papers

Recent·Most cited

The chromatin landscape of healthy and injured cell types in the human kidney

Debora L. Gisch, Michelle Brennan, Blue B. Lake, Jeannine M. Basta, Mark S. Keller, Ricardo Melo Ferreira, Shreeram Akilesh, Reetika R. Ghag, Charles Lu, Ying‐Hua Cheng, Kimberly S. Collins, Samir V. Parikh, Brad H. Rovin, Lynn Robbins, Lisa Stout, , Joana P. Gonçalves

The paper defines the chromatin landscape of healthy and injured kidney cells using multi-omics data, identifying regulatory elements and transcription factor networks involved in injury response.

Nature Communications · Jan 10, 2024Peer-reviewedMolecular Biology

Deletion of NuRD component Mta2 in nephron progenitor cells causes developmentally programmed FSGS

Jeannine M. Basta, Lynn Robbins, Lisa Stout, Michelle Brennan, John P. Shapiro, Mary Chen, Darcy R. Denner, Ángel Baldán, Nidia Cordeiro Messias, Sethu M. Madhavan, Samir V. Parikh, Michael I. Rauchman

This study shows that deleting Mta2 in nephron progenitor cells leads to low nephron number, which causes FSGS and CKD through impaired mitochondrial lipid metabolism and gene regulation.

bioRxiv · Oct 18, 2023 · PreprintDevelopmental Biology

Analysis of FGF20-regulated genes in organ of Corti progenitors by translating ribosome affinity purification

Lu M. Yang, Lisa Stout, Michael I. Rauchman, David M. Ornitz

The paper uses TRAPseq to identify FGF20-regulated genes in mouse organ of Corti progenitors, finding genes involved in hair cell differentiation and hearing loss.

Developmental Dynamics · Jun 3, 2020Peer-reviewedDevelopmental Biology