Oktay Ismail Kaplan

11PUBLICATIONS
26CO-AUTHORS
Cancer geneticsCell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Structural properties of condensed matterGenome structure and regulation
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Publications (11)

|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

|Jul 11, 2024
CilioGenics: an integrated method and database for predicting novel ciliary genes.

Mustafa S Pir, Efe Begar, Ferhan Yenisert

|Nov 07, 2023
Matching variants for functional characterization of genetic variants.

Sebiha Cevik, Pei Zhao, Atiyye Zorluer

|Aug 05, 2023
CiliaMiner: an integrated database for ciliopathy genes and ciliopathies.

Merve Gül Turan, Mehmet Emin Orhan, Sebiha Cevik

|Aug 02, 2023
RPI-1 (human DCDC2) displays functional redundancy with Nephronophthisis 4 in regulating cilia biogenesis in C. elegans.

Oktay I Kaplan

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Frequent Collaborators

3 joint publications

Sukru Sadik Oner

2 joint publications

Sebiha Cevik

2 joint publications

Mustafa S Pir

2 joint publications

Ferhan Yenisert