Author

Bruno Marino

Sapienza University of Rome

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Biology Disciplines

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Genetics· 1

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 Carolina PutottoiD· 1 shared Carrie E. BeardeniD· 1 shared Christian R. MarshalliD· 1 shared Claudia VingerhoetsiD· 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

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, Donna M. McDonald‐McGinn, Terrence Blaine Crowley, Daniel E. McGinn, Oanh Tran, Daniella Miller, Elaine H. Zackai, H. Richard Johnston, Eva W.C. Chow, Jacob A. S. Vorstman, Claudia Vingerhoets, Thérèse van Amelsvoort, Doron Gothelf, , 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.

bioRxiv · Sep 30, 2022 · PreprintGenetics