Author

Robert E. Settlage

Virginia TechORCID 0000-0002-1354-7609Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:genome assembly· 1 Organism:mouse· 1

Frequent Co-Authors

Austin ComptoniD· 1 shared Chelsi Jeter· 1 shared Chujia CheniD· 1 shared Chunhong Mao· 1 shared Cynthia J. TifftiD· 1 shared David R. AdamsiD· 1 shared Dustin Miller· 1 shared Graydon B. GonsalveziD· 1 shared

Activity by Year

2020-2020 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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1 shared paperGenomics

Austin ComptonORCID

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3 papers

Recent·Most cited

GenomicsG3 Genes Genomes GeneticsPeer-reviewedSep 3, 2020

The beginning of the end: a chromosomal assembly of the New World malaria mosquito ends with a novel telomere

Austin Compton, Jiangtao Liang, Chujia Chen…·Zhijian Tu

This paper presents a telomere-to-telomere genome assembly of Anopheles albimanus using advanced sequencing technologies, revealing novel telomeric repeats and previously uncharacterized genomic regions.

31 citations

whole-genome sequencingexperimental assay

𝕏 PostBluesky

NeurosciencebioRxivPreprintMar 13, 2020

Identification of a molecular fingerprint for synaptic glia

Ryan W. Castro, Thomas Taetzsch, Sydney V. Doss…·Gregorio Valdez

The paper identifies molecular markers for perisynaptic Schwann cells (PSCs) and shows they have a unique molecular signature related to synapse function.

1 citation

mousebulk RNA-seq

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