Oktay I. Kaplan

Kayseri, Turkey

Last Updated: 09/26/2026

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Found 20 publications

Bi-allelic variants in OLA1 cause a neurodevelopmental disorder with joint hypermobility.

Bi-allelic variants in OLA1 cause a neurodevelopmental disorder with joint hypermobility.

Journal: American journal of human genetics

Published: September 16, 2025

A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia.

A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia.

Journal: European journal of human genetics : EJHG

Published: January 26, 2025

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow.

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow.

Journal: Life science alliance

Published: March 11, 2024

ARL13B regulates juxtaposed cilia-cilia elongation in BBSome dependent manner in Caenorhabditis elegans.

ARL13B regulates juxtaposed cilia-cilia elongation in BBSome dependent manner in Caenorhabditis elegans.

Journal: iScience

Published: February 02, 2024

Effects of essential oil mixtures on expression of genes involved in lipogenesis and fatty acid oxidation in geese (Anser anser).

Effects of essential oil mixtures on expression of genes involved in lipogenesis and fatty acid oxidation in geese (Anser anser).

Journal: Tropical animal health and production

Published: August 18, 2023

CilioGenics: an integrated method and database for predicting novel ciliary genes.

CilioGenics: an integrated method and database for predicting novel ciliary genes.

Journal: Nucleic acids research

Published: April 11, 2023

Matching variants for functional characterization of genetic variants.

Matching variants for functional characterization of genetic variants.

Journal: G3 (Bethesda, Md.)

Published: February 22, 2023

CiliaMiner: an integrated database for ciliopathy genes and ciliopathies.

CiliaMiner: an integrated database for ciliopathy genes and ciliopathies.

Journal: Database : the journal of biological databases and curation

Published: December 08, 2022

ConVarT: Search Engine for Missense Variants Between Humans and Other Organisms.

ConVarT: Search Engine for Missense Variants Between Humans and Other Organisms.

Journal: Current protocols

Published: November 22, 2022

WDR31 displays functional redundancy with GTPase-activating proteins (GAPs) ELMOD and RP2 in regulating IFT complex and recruiting the BBSome to cilium.

WDR31 displays functional redundancy with GTPase-activating proteins (GAPs) ELMOD and RP2 in regulating IFT complex and recruiting the BBSome to cilium.

Journal: Life science alliance

Published: November 21, 2022

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

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

Journal: Turkish journal of biology = Turk biyoloji dergisi

Published: June 22, 2022

Protocol for determining the average speed and frequency of kinesin and dynein-driven intraflagellar transport (IFT) in C. elegans.

Protocol for determining the average speed and frequency of kinesin and dynein-driven intraflagellar transport (IFT) in C. elegans.

Journal: STAR protocols

Published: March 31, 2022

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Last Updated: 09/26/2026