Author

Sahar Sadat Sedighzadeh

ORCID 0000-0002-6973-4809Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1 Organism:zebrafish· 1

Frequent Co-Authors

A. Elsayed· 1 shared A. L. Bruel· 1 shared Alireza SedaghatiD· 1 shared Anna Wiemers· 1 shared Barbara VonaiD· 1 shared Bernd AuberiD· 1 shared C. Phillipe· 1 shared Cassidy PetreeiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Elsayed

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1 paper

Recent·Most cited

XPOT Deficiency causes a human disorder through impaired tRNA nuclear export

Sandra v. Hardenberg, Indra Niehaus, Anna Wiemers, Tobias Rothoeft, K. Huang, Cassidy Petree, V. Schäffer, C. Phillipe, A. L. Bruel, Klaus Warnatz, Mina Zamani, R. Ahmadi, Alireza Sedaghat, Seiamak Bahram, Sahar Sadat Sedighzadeh, , Bernd Auber

This study identifies XPOT deficiency as a human disorder causing immune defects, hearing loss, and developmental issues through impaired tRNA nuclear export.

medRxiv · Feb 4, 2026 · PreprintGenetic & Genomic Medicine