Author

Ana B.W. Greenberg

Harvard UniversityORCID 0009-0002-6930-8241Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Andrés Moreno-De-LucaiD· 2 shared Benjamin C. ReevesiD· 2 shared Bob S. CarteriD· 2 shared Carol J. Nelson-WilliamsiD· 2 shared Garrett AllingtoniD· 2 shared Hannah Louise SmithiD· 2 shared Kedous Y. MekbibiD· 2 shared Kristopher Thomas KahleiD· 2 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersNeuroscience

Andrés Moreno-De-LucaORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Dual impact of PTEN mutation on CSF dynamics and cortical networks via the dysregulation of neural precursors and their interneuron descendants

Tyrone DeSpenza, Emre Kiziltug, Garrett Allington, Daniel G. Barson, David A. O’Connor, Stephanie M. Robert, Kedous Y. Mekbib, Pranav Nanda, Ana B.W. Greenberg, Amrita Singh, Phan Q. Duy, Francesca Mandino, Shujuan Zhao, Anna Y. Lynn, Benjamin C. Reeves, , Kristopher Thomas Kahle

This study shows PTEN mutations cause ventriculomegaly and cortical network dysfunction through neural precursor and interneuron dysregulation, with mTORC1 inhibition offering therapeutic potential.

bioRxiv · Mar 18, 2023 · PreprintNeuroscience

Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations

Shujuan Zhao, Kedous Y. Mekbib, Martijn A. van der Ent, Garrett Allington, Andrew E. Prendergast, Jocelyn E. Chau, Hannah Louise Smith, John P. Shohfi, Jack Ocken, Daniel Durán, Charuta Gavankar Furey, Hao Thi Le, Phan Q. Duy, Benjamin C. Reeves, Junhui Zhang, , Kristopher Thomas Kahle

The paper identifies genetic variants in RASA1 and EPHB4 associated with vein of Galen malformations through exome analysis and single-cell transcriptomics.

bioRxiv · Mar 18, 2023 · PreprintGenomics