Author

Sophie D. Curie

Johns Hopkins UniversityORCID 0000-0002-1351-644XUnclaimed 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:differential expression· 1 Organism:human· 1 Assay:metabolomics· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Arianna Franca AnzmanniD· 1 shared Courtney E. Woods· 1 shared David L. ValleiD· 1 shared Débora Romeo BertolaiD· 1 shared Felicity A. Collins· 1 shared Guilherme Lopes YamamotoiD· 1 shared John ChristodoulouiD· 1 shared Julie A. JurgensiD· 1 shared

Activity by Year

2019-2019 · 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

Arianna Franca AnzmannORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

GeneticsbioRxivPreprintDec 19, 2019

Loss of function variants in PCYT1A causing spondylometaphyseal dysplasia with cone/rod dystrophy have broad consequences on lipid metabolism, chondrocyte differentiation, and lipid droplet formation.

Julie A. Jurgens, Suming Chen, Nara Lygia de Macena Sobreira…·David L. Valle

This study investigates the effects of PCYT1A variants on lipid metabolism, chondrocyte differentiation, and lipid droplet formation using cellular models and lipidomics.

DOI 10.1101/2019.12.19.882191

humanproteomics

𝕏 PostBluesky