Author

Ebru Erzurumluoğlu Gökalp

Eskişehir Osmangazi UniversityORCID 0000-0002-1275-5174Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Afrooz RashnonejadiD· 1 shared Allison M. BradburyiD· 1 shared Ben Kelly· 1 shared Beyhan Durak ArasiD· 1 shared Burçak ÖzeşiD· 1 shared Colin T. MaguireiD· 1 shared Devi Jaganathan· 1 shared Duygu CinariD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Afrooz RashnonejadORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

REMEDY: REpair of heterozygous Mutations independent of Exogenous Donor template with high efficiency using allele specific CRISPR targeting and HDR enhancers

Yasemin Sezgin, Genesis Snyder, Noushin Saljoughian, Colin T. Maguire, Ebru Erzurumluoğlu Gökalp, Devi Jaganathan, Eleonora Silvana D'Ambrosio, Burçak Özeş, Gregory L. Wheeler, Ben Kelly, Mark E. Hester, Zarife Sahenk, Sriram Vaidyanathan, Afrooz Rashnonejad, Jerry R. Mendell, , Meisam Naeimi Kararoudi

REMEDY enables efficient repair of heterozygous mutations in human and mouse cells without exogenous donor DNA by using CRISPR-induced DSBs and HDR enhancers.

bioRxiv · May 29, 2025 · PreprintGenetics

Uncovering the Dual Role of Mitochondrial and Nuclear DNA Variants in Pediatric Cardiomyopathies

Mehmet Arda Temena, Ebru Erzurumluoğlu Gökalp, Ezgi Susam, Duygu Cinar, Hikmet Kıztanır, Pelin Köşger, Beyhan Durak Aras, Sevilhan Artan, Oğuz Cilingir

The paper identifies pathogenic mitochondrial and nuclear DNA variants in pediatric cardiomyopathy patients and highlights their potential interconnected roles in disease mechanisms.

Scientific Reports · May 14, 2025Peer-reviewedGenetic & Genomic Medicine