Author

Adriana Cherskov

Yale UniversityORCID 0000-0002-9905-2665Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Nenad ŠestaniD· 2 shared Shaojie MaiD· 2 shared Aastha SindhwaniiD· 1 shared Akemi ShibataiD· 1 shared Alvaro DuqueiD· 1 shared Amir KargeriD· 1 shared Amrita K. SinghiD· 1 shared Ana SpajiciD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersNeuroscience

Nenad ŠestanORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Human-specific features of the cerebellum and ZP2-regulated synapse development

Suel–Kee Kim, Adriana Cherskov, Aastha Sindhwani, Sang-Hun Choi, Hyojin Kim, Mingli Li, Menglei Zhang, Xoel Mato-Blanco, Yuting Liu, Nicola Micali, David Matthew Young, Mark Estación, Yueqi Zhang, Jose Manuel Ruiz-Jiménez, Anandita Nadkarni, , Nenad Šestan

The paper identifies human-specific transcriptomic and regulatory features in the cerebellum, including ZP2's role in synapse development and regulation.

Cell · Mar 1, 2026Peer-reviewedNeuroscience

A novel SMARCC1-mutant BAFopathy implicates epigenetic dysregulation of neural progenitors in hydrocephalus

Amrita K. Singh, Stephen Viviano, Garrett Allington, Stephen McGee, Emre Kiziltug, Kedous Y. Mekbib, John P. Shohfi, Phan Q. Duy, Tyrone DeSpenza, Charuta Gavankar Furey, Benjamin C. Reeves, Hannah Louise Smith, Shaojie Ma, André M. M. Sousa, Adriana Cherskov, , Kristopher Thomas Kahle

This study identifies SMARCC1 mutations as a cause of congenital hydrocephalus, showing they lead to neural progenitor dysfunction and a new syndrome called SaDDS.

medRxiv · Mar 19, 2023 · PreprintGenetic & Genomic Medicine