Author

M. Arreola

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· 2

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:genetic perturbation / CRISPR· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:scRNA-seq· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. Awani· 1 shared A. DeVilbiss· 1 shared D. Dever· 1 shared G. Benegiamo· 1 shared J. Auwerx· 1 shared J. K. Pritchard· 1 shared J. Mohammed· 1 shared J. Tycko· 1 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

A. Awani

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Author profile →

2 papers

Recent·Most cited

A genome-wide genetic screen uncovers novel determinants of human pigmentation

V. K. Bajpai, T. Swigut, J. Mohammed, J. Tycko, S. Naqvi, M. Arreola, T. Kim, N. Arora, J. K. Pritchard, M. C. Bassik, J. Wyscoka

A genome-wide CRISPR-Cas9 screen identifies novel genes regulating melanogenesis, many upregulated in dark skin melanocytes and associated with skin color variation.

bioRxiv · Sep 29, 2021 · PreprintCell Biology

Reticular Dysgenesis-associated Adenylate Kinase 2 deficiency causes failure of myelopoiesis through disordered purine metabolism

W. Wang, A. DeVilbiss, M. Arreola, T. Mathews, Z. Zhao, M. Martin-Sandoval, G. Benegiamo, A. Awani, L. Goeminne, D. Dever, Y. Nakauchi, M. Pavel-Dinu, W. Al-Herz, L. Noratangelo, M. H. Porteus, , K. G. Weinacht

This study shows AK2 deficiency disrupts mitochondrial metabolism, causing purine metabolism disorder and myelopoiesis failure through AMP accumulation and NAD+ depletion.

bioRxiv · Jul 5, 2021 · PreprintCell Biology