Author

Hülya Kayserili

Koç UniversityORCID 0000-0003-0376-499XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Organism:zebrafish· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:statistical model· 1

Frequent Co-Authors

Bertrand BoissoniD· 2 shared Bruno ReversadeiD· 2 shared Elanur YılmaziD· 2 shared Jean‐Laurent CasanovaiD· 2 shared Ricardo Moreno TraspasiD· 2 shared Abigail LohiD· 1 shared Afaf Alsubhi· 1 shared Aida Maria Bertoli‐AvellaiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Bertrand BoissonORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintSep 29, 2026

Snurportin-1 maintains muscle niche integrity and myogenic progenitor homeostasis

Hilal Pırıl Saraçoğlu, Marwan Nashabat, Duygu Naz Kutlu…·Nathalie Escande‐Beillard

This study identifies Snurportin-1 as critical for skeletal muscle homeostasis by linking RNA processing to extracellular niche integrity and myogenic progenitor maintenance using a zebrafish model.

DOI 10.64898/2026.09.24.749599

zebrafishbulk RNA-seq

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Genetic & Genomic MedicineScience ImmunologyPeer-reviewedSep 16, 2022

DPP9 deficiency: an inflammasomopathy which can be rescued by lowering NLRP1/IL-1 signaling

Cassandra R. Harapas, Kim S. Robinson, Kenneth Lay…·Bruno Reversade

This study identifies DPP9 deficiency as a Mendelian disorder causing inflammasome hyperactivity, which can be rescued by reducing NLRP1/IL-1 signaling in mice.

58 citationstop 5%

humanstatistical model

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Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedMay 25, 2021

Loss of C2orf69 defines a fatal auto-inflammatory mitochondriopathy in Humans and Zebrafish

Hui Hui Wong, Sze Hwee Seet, Michael Maier…·Bruno Reversade

The paper identifies C2orf69 deficiency as a cause of a fatal auto-inflammatory syndrome in humans and zebrafish, affecting mitochondrial function and immune/cNS development.

23 citations

humanzebrafish

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