Author

E. Petretto

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

Biology Disciplines

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Cell Biology· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Research Focus:clustering· 1 Approach:experimental assay· 1

Frequent Co-Authors

A. L. M. Tan· 1 shared A. Moreno-Moral· 1 shared B. Kerouantan· 1 shared B. Reversade· 1 shared C. L. Wee· 1 shared C. Liang· 1 shared C. Mary· 1 shared C. Tang· 1 shared

Activity by Year

2018-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperCell Biology

A. L. M. Tan

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3 papers

Recent·Most cited

A trans-eQTL network regulates osteoclast multinucleation and bone mass

M. Pereira, J.-H. Ko, J. Logan, H. Protheroe, K.-B. Kim, A. L. M. Tan, K.-S. Park, M. Rotival, E. Petretto, J. H. D. Bassett, G. R. Williams, J. Behmoaras

The paper identifies a trans-eQTL network (MMnet) that regulates osteoclast multinucleation and bone mass in mice and humans.

bioRxiv · Feb 13, 2020Cell Biology

BRAWNIN: A sORF-encoded Peptide Essential for Vertebrate Mitochondrial Complex III Assembly

S. Zhang, C. Liang, C. Mary, B. Kerouantan, J. Francisco, N. S. Jagannathan, V. Olexiouk, J. H. Peh, C. Tang, G. Fidelito, S. Nama, R.-K. Cheng, C. L. Wee, L. C. Wang, P. D. Roggli, , L. Ho

The paper identifies BRAWNIN, a sORF-encoded peptide critical for vertebrate mitochondrial complex III assembly, showing its role in oxidative phosphorylation and metabolic function.

bioRxiv · Jan 31, 2020 · PreprintCell Biology

In vivo generation of post-infarct mouse cardiac muscle by cardiomyocyte progenitors produced with a reproducible laminin-promoted human stem cell differentiation system

L. Yap, J.-W. Wang, A. Moreno-Moral, L. Y. Chong, Y. Sun, N. Harmston, X. Wang, S. Y. Chong, M. K. Ohman, H. Wei, R. Bunte, S. Ghosh, S. Cook, O. Hovatta, D. P. V. de Kleijn, , K. Tryggvason

This paper develops a reproducible method to generate cardiac muscle progenitors from human stem cells using laminin-221, which can form human heart muscle in vivo after transplantation.

bioRxiv · Nov 26, 2018 · PreprintCell Biology