Author

Marco Armando

Centre Hospitalier Universitaire VaudoisORCID 0000-0001-7074-7212Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alessandra SolidaiD· 1 shared Ann SwilleniD· 1 shared Anne S. BassettiD· 1 shared Antoine KlauseriD· 1 shared Bernice E. MorrowiD· 1 shared Beverly S. EmanueliD· 1 shared Bruno Marino· 1 shared Carolina PutottoiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperNeuroscience

Alessandra SolidaORCID

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2 papers

Recent·Most cited

NeuroscienceImaging NeurosciencePeer-reviewedJan 1, 2026

High-resolution whole-brain magnetic resonance spectroscopic imaging in youth at risk for psychosis

Edgar Céléreau, Federico Lucchetti, Yasser Alemán‐Gómez…·Paul Klauser

This study uses high-resolution 3D-MRSI to assess neurometabolite differences in youth at risk for psychosis compared to controls, finding elevated tNAA and Ins in specific brain regions.

4 citationstop 2%

humanimaging

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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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