Author

Beatrice Costa

Gladstone InstitutesORCID 0000-0002-3508-8757Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:gene regulatory network inference· 2 Organism:human· 2 Assay:CRISPR screen· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Organism:rat· 1 Approach:statistical model· 1

Frequent Co-Authors

Lisa P. EliaiD· 2 shared Steven M. FinkbeineriD· 2 shared Zachary TokunoiD· 2 shared Amy PetersoniD· 1 shared Andrew E. JaffeiD· 1 shared Austin R. HolubiD· 1 shared Bianca Barth· 1 shared Ching‐Chieh ChouiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 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

2 shared papersCell Biology

Lisa P. EliaORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Cell BiologybioRxivPreprintOct 28, 2026

Parkin deficiency rewires the genetic dependencies that govern neuronal survival

Shijie Wang, Daniel R. Gulbranson, Beatrice Costa…·Steven M. Finkbeiner

This study shows that Parkin deficiency alters genetic dependencies for neuronal survival, identifying key pathways and genes involved in this rewiring.

DOI 10.64898/2026.10.27.762340

ratCRISPR screen

𝕏 PostBluesky

BioinformaticsbioRxivPreprintMar 22, 2023

A Comprehensive Enumeration of the Human Proteostasis Network. 2. Components of the Autophagy-Lysosome Pathway

Overall coordination, Suzanne Elsasser, Lisa P. Elia…·Ralph A. Nixon

The paper curates a list of 838 high-confidence components of the autophagy-lysosome pathway as part of a comprehensive effort to define the human proteostasis network.

24 citations

humanproteomics

𝕏 PostBluesky

BioinformaticsScience AdvancesPeer-reviewedJun 10, 2020

Incomplete annotation of disease-associated genes is limiting our understanding of Mendelian and complex neurogenetic disorders

David Zhang, Sebastian Guelfi, Sonia García-Ruiz…·Mina Ryten

The paper identifies and validates novel transcription regions across tissues, improving gene annotation for 63% of OMIM-morbid genes and highlights tissue-specific and functionally significant variants.

66 citationstop 3%

humanwhole-exome sequencing

𝕏 PostBluesky