Author

Christophe C. Faure

Centre Hospitalier Universitaire Sainte-JustineORCID 0000-0002-2998-8935Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aaron M. ZorniD· 1 shared Adhish Kashyap· 1 shared Alan P. KennyiD· 1 shared Alassane Gary· 1 shared Ann AspirotiD· 1 shared Anu DavidiD· 1 shared David T. Schindel· 1 shared Elizabeth FialkowskiiD· 1 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aaron M. ZornORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintMay 23, 2025

GDNF regenerates the missing enteric nervous system of Hirschsprung mice via non-canonical signaling in diverse subtypes of tissue-resident progenitors

Alassane Gary, Rodolphe Soret, Marie A. Lefevre…·Nicolas Pilon

This study shows GDNF regenerates the missing enteric nervous system in Hirschsprung mice through non-canonical signaling in tissue-resident progenitors, suggesting potential for broader therapeutic applications.

2 citations

mouseexperimental assay

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Genetic & Genomic MedicineHuman Genetics and Genomics AdvancesPeer-reviewedApr 16, 2022

Identification and validation of novel candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas

Guojie Zhong, Priyanka R. Ahimaz, Nicole A. Edwards…·Wendy K. Chung

The paper identifies novel risk genes associated with EA/TEF through whole genome sequencing and functional validation using CRISPR-Cas9 in Xenopus.

14 citations

humanwhole-genome sequencing

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Developmental BiologybioRxivPreprintFeb 14, 2022

Directed differentiation of EA/TEF patient-derived induced pluripotent stem cells into esophageal epithelial organoids reveal SOX2 dysregulation at the anterior foregut stage

Suleen Raad, Anu David, Mélanie Sagniez…·Christophe C. Faure

The paper differentiates iPSCs from EA/TEF patients and healthy donors into esophageal organoids, identifying SOX2 and NKX2.1 dysregulation as potential causes of foregut compartmentalization defects.

DOI 10.1101/2022.02.14.480418

humanbulk RNA-seq

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