Author

Tzipora C. Falik Zaccai

Bar-Ilan UniversityORCID 0000-0003-0065-1922Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Aviram ShemeniD· 1 shared Danielle Klinger· 1 shared Dina Schneidman‐DuhovnyiD· 1 shared Ehud BanneiD· 1 shared Esther S. BrielleiD· 1 shared Hagay LadanyiD· 1 shared Hanna MandeliD· 1 shared Herman WoloskeriD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperNeuroscience

Aviram ShemenORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

NeurosciencebioRxivPreprintApr 25, 2025

Dysregulation of Multiple Solute Carrier genes and Metabolic Deficits in SLC1A4-Mutant Human iPSC-Derived Hippocampal Neurons

Ritu Nayak, Omveer Sharma, Liron Mizrahi…·Shani Stern

This study investigates SLC1A4 mutations in human iPSC-derived neurons, revealing metabolic and synaptic deficits linked to amino acid transport dysfunction and neurodevelopmental disorders.

3 citations

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsAmerican Journal of Medical Genetics Part B Neuropsychiatric GeneticsPeer-reviewedAug 19, 2020

Structural analysis of de novo STXBP1 mutation in complex with syntaxin 1A reveals a major alteration in the interaction interface in a child with developmental delay and spasticity

Ehud Banne, Tzipora C. Falik Zaccai, Esther S. Brielle…·Michal Linial B

The paper identifies a de novo STXBP1 mutation in a child with developmental delay and spasticity, showing how it disrupts the STXBP1-syntaxin 1A interaction through structural analysis.

8 citations

humanprotein structure

𝕏 PostBluesky