Author

Tuğba Kalaycı

Istanbul UniversityORCID 0000-0002-9963-5916Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

Zehra Oya UyguneriD· 2 shared Alexander ZimprichiD· 1 shared Alexandra DürriD· 1 shared Ángeles Montero· 1 shared Anna L. PeljtoiD· 1 shared Anthea CheungiD· 1 shared Birsen KaramaniD· 1 shared Bonnie R. SullivaniD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Zehra Oya UygunerORCID

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2 papers

Recent·Most cited

Rare bi-allelic loss-of-function variants in the LRRK2 kinase cause interstitial lung disease

Tuğba Kalaycı, Kathryn A. Wikenheiser‐Brokamp, Sara Gomes, Eshaan S. Rawat, Anna L. Peljto, Anthea Cheung, Sevinç Çitak, Mustafa Vayvada, Ángeles Montero, Nesrin Moğulkoç, N. Gulfer Okumus, İlknur Süer, Joseph A. Kitzmiller, Cheng-Lun Na, Xinyuan Li, , Esther M. Sammler

This study identifies biallelic LRRK2 loss-of-function variants as a cause of interstitial lung disease, showing reduced LRRK2 protein and impaired lung function in affected individuals.

medRxiv · May 19, 2026 · PreprintGenetic & Genomic Medicine

Basic helix-loop-helix transcription factor BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, tone and movement abnormalities

Carolyn Le, Emanuela Argilli, Elizabeth George, Tuğba Kalaycı, Zehra Oya Uyguner, Birsen Karaman, Tanju Demirören, Stephanie P. DiTroia, Delphine Héron, Isabelle Sabatier, Lance H. Rodan, Katta M. Girisha, Periyasamy Radhakrishnan, Carol Saunders, Bonnie R. Sullivan, , Elliott H. Sherr

medRxiv · Oct 11, 2024 · PreprintGenetic & Genomic Medicine