Author

Emilie Auxerre-Plantié

Centre National de la Recherche ScientifiqueORCID 0000-0002-8703-7636Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:Drosophila· 3 Approach:experimental assay· 3 Research Focus:differential expression· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Yoan RenaudiD· 2 shared Aline Huguet-LachoniD· 1 shared Andreas PerrotiD· 1 shared Caroline ChoquetiD· 1 shared Cemil Özcelik· 1 shared Christian MühlfeldiD· 1 shared Cristiana DondiiD· 1 shared Cristobal G. dos RemediosiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersMolecular Biology

Yoan RenaudORCID

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3 papers

Recent·Most cited

Molecular BiologybioRxivPreprintSep 15, 2023

Adenine methylation is very scarce in the drosophila genome and not erased by the Ten Eleven Translocation dioxygenase.

Manon Boulet, Guerric Gilbert, Yoan Renaud…·Lucas Waltzer

The paper investigates 6mA DNA modification in drosophila, finding it present at very low levels and not erased by TET, suggesting TET acts non-enzymatically.

1 citation

DrosophilaDNA methylation

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GeneticsDisease Models & MechanismsPeer-reviewedOct 8, 2020

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot and its functional evaluation in the Drosophila heart

Emilie Auxerre-Plantié, Tanja Nielsen, Marcel Grunert…·Silke Sperling

The paper identifies MYOM2 as a candidate gene for hypertrophic cardiomyopathy and Tetralogy of Fallot and shows its functional role in heart development through Drosophila models.

36 citations

Drosophilaexperimental assay

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GenomicseLifePeer-reviewedDec 12, 2019

Straightjacket/α 2δ 3 deregulation is associated with cardiac conduction defects in Myotonic Dystrophy type 1

Emilie Auxerre-Plantié, Masayuki Nakamori, Yoan Renaud…·Krzysztof Jagla

The paper identifies straightjacket/α2δ3 deregulation as a contributor to cardiac conduction defects in DM1 by showing its overexpression in fly models and human patients.

14 citations

Drosophilamouse

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