Kadri Karaer

6PUBLICATIONS
9CO-AUTHORS
NeurogeneticsNumerical modelling and mechanical characterisationNeurology and neuromuscular diseasesCraniofacial biology
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Publications (6)

|Jul 03, 2026
Clinical utility and genetic landscape of exome sequencing in a large pediatric epilepsy cohort: Insights from a Turkish tertiary care center.

|May 05, 2026
A Rare Case: NGLY1 Deficiency and Diaphragmatic Eventration.

|Jan 03, 2025
NRXN2 Homozygous Variant Identified in a Family with Global Developmental Delay, Severe Intellectual Disability, EEG Abnormalities and Speech Delay: A new Syndrome?

Derya Karaer, Ayşe Aysima Özçelik, Kadri Karaer

|Jun 27, 2022
Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias.

Akgün Ölmez, Gökhan Ozan Çetin, Kadri Karaer

|Feb 28, 2022
Two novel variants in SCARF2 gene underlie van den Ende-Gupta syndrome.

Derya Karaer, Kadri Karaer

|Mar 16, 2021
Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort.

Gül Keskin, Kadri Karaer, Zübeyde Uçar Gündoğar

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Frequent Collaborators

2 joint publications

Derya Karaer

1 joint publications

Gül Keskin

1 joint publications

Zübeyde Uçar Gündoğar

1 joint publications

Akgün Ölmez