Author

Maude Schneider

University of GenevaORCID 0000-0001-7147-8915Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:mouse· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ann SwilleniD· 1 shared Anne S. BassettiD· 1 shared Bernice E. MorrowiD· 1 shared Beverly S. EmanueliD· 1 shared Bruno Marino· 1 shared Carolina PutottoiD· 1 shared Carrie E. BeardeniD· 1 shared Christian R. MarshalliD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Ann SwillenORCID

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintSep 30, 2022

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

Yingjie Zhao, Yujue Wang, Lijie Shi…·Bernice E. Morrow

The paper identifies chromatin regulatory genes as genetic modifiers of conotruncal heart defects in 22q11.2 deletion syndrome and links them to sporadic congenital heart disease.

DOI 10.1101/2022.09.30.507111

mousewhole-genome sequencing

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