Author

Teddy Fauquier

InsermORCID 0000-0003-1132-9402Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Anne BarlieriD· 2 shared Heather EtcheversiD· 2 shared Anne PoliardiD· 1 shared Elise MaréchaliD· 1 shared Frédéric CastinettiiD· 1 shared Grégoire MondielliiD· 1 shared Kilian Henry· 1 shared Mathias MorenoiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersDevelopmental Biology

Anne BarlierORCID

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2 papers

Recent·Most cited

Developmental BiologyeLifePeer-reviewedNov 28, 2024

Modeling corticotroph deficiency with pituitary organoids supports the functional role of NFKB2 in human pituitary differentiation

Thi Thom Mac, Teddy Fauquier, Nicolas Jullien…·Thierry Christian Brue

This study uses CRISPR/Cas9-edited human pituitary organoids to show that NFKB2 mutations impair corticotroph differentiation, confirming its role in ACTHD.

1 citation

humanbulk RNA-seq

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Developmental BiologyFrontiers in Cell and Developmental BiologyPeer-reviewedOct 24, 2022

Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signalling

Elise Maréchal, Anne Poliard, Kilian Henry…·Heather Etchevers

This study investigates how somatic Pik3ca mutations in neural crest and related lineages cause congenital malformations and vascular anomalies in mice, with implications for human PIK3CA-related disorders.

9 citations

mouseexperimental assay

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