Sukru Sadik Oner
3PUBLICATIONS
21CO-AUTHORS
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Publications (3)
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|Jul 04, 2025
A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia.Abdullah Sezer, Sukru S Oner, Hanife Saat
|Aug 21, 2024
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow.Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano
|May 19, 2023
WDR31 displays functional redundancy with GTPase-activating proteins (GAPs) ELMOD and RP2 in regulating IFT complex and recruiting the BBSome to cilium.Sebiha Cevik, Xiaoyu Peng, Tina Beyer
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Frequent Collaborators
3 joint publications
Oktay I Kaplan
2 joint publications
Ferhan Yenisert
1 joint publications
Sebiha Cevik
1 joint publications
Tina Beyer
1 joint publications
Mustafa S Pir
1 joint publications
Karsten Boldt
1 joint publications
Miray Cakiroglu
1 joint publications
Abdullah Sezer
1 joint publications
Hanife Saat
1 joint publications
Asli Erol
