Author

Silvia Cereghini

Centre National de la Recherche ScientifiqueORCID 0000-0002-1562-089XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 3

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Assay:scRNA-seq· 2 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Adrian S. WoolfiD· 1 shared Albert Chesneau· 1 shared Alexis EschstruthiD· 1 shared Alison Hensley· 1 shared Alla Vash‐MargitaiD· 1 shared Andrew Henrik SinclairiD· 1 shared Ella ThomsoniD· 1 shared Emanuele PelosiiD· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperDevelopmental Biology

Adrian S. WoolfORCID

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3 papers

Recent·Most cited

Developmental BiologyStem Cell ReportsPeer-reviewedMay 23, 2024

Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations

Ioannis Bantounas, Kirsty M. Rooney, Filipa M. Lopes…·Susan J. Kimber

This study uses HNF1B mutant kidney organoids to reveal molecular and physiological defects in dysplastic kidney malformations and identify potential therapeutic targets.

16 citations

humanscRNA-seq

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Developmental BiologyScientific ReportsPeer-reviewedNov 19, 2022

Hnf1b renal expression directed by a distal enhancer responsive to Pax8

Laura Goea, Isabelle Buisson, Valérie Bello…·Muriel Umbhauer

The paper identifies a distal enhancer, CNS1, that drives Hnf1b renal expression and is responsive to Pax8 in Xenopus and mammalian renal cells.

7 citations

statistical modelgene regulatory network inference

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Developmental BiologybioRxivPreprintApr 26, 2022

Functional genomics analysis identifies impairment of HNF1B function as a cause of Mayer-Rokitansky-Küster-Hauser syndrome.

Ella Thomson, Minh Tran, Gorjana Robevska…·Emanuele Pelosi

The paper identifies HNF1B dysfunction as a cause of Mayer-Rokitansky-Küster-Hauser syndrome using genomic analysis and mouse models.

1 citation

mousescRNA-seq

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