Author

Shivang Khandelwal

Hebrew University of JerusalemORCID 0000-0001-7478-3536Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Anurag Prabhu· 1 shared Ela Elyada· 1 shared Manar Abu Diab· 1 shared Reut Japha· 1 shared Rotem KarniiD· 1 shared Zahava SiegfriediD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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6 top collaborators · 15 mutual co-author links

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1 shared paperGenetics

Anurag Prabhu

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintMar 18, 2026

Molecular characterization of the heterozygous loss of function mutations in the X-linked PCDH19 gene causing PCDH19-Cluster Epilepsy

Shivang Khandelwal, Ela Elyada, Reut Japha…·Rotem Karni

The paper investigates PCDH19-Cluster Epilepsy by generating mouse and human models, identifying differentially expressed genes and morphological changes linked to PCDH19 mutations.

DOI 10.64898/2026.03.16.712128

mousehuman

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