Gül Ünsel-Bolat

20PUBLICATIONS
47CO-AUTHORS
Medical infection agents (incl. prions)Paediatrics not elsewhere classifiedNeurogeneticsGene mappingGenome structure and regulation
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Publications (20)

|Jul 19, 2026
Rare Variants in Purinergic P2X Receptor Genes (P2RX4, P2RX5, P2RX7) in Individuals With Autism Spectrum Disorder: An Exploratory Study.

|May 25, 2026
TRMT10A-Related Neurodevelopmental Disorder Without Metabolic Findings.

|Apr 27, 2026
Testing DAT1 and DRD4 Genes in Attention Deficit Hyperactivity Disorder Using a Wide Spectrum of Neurocognitive Batteries.

|Feb 24, 2026
ATP6V0A2-Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant.

Zeynep Esener, Murat Öztürk, Esra Habiloğlu

|Feb 18, 2026
Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition.

Hilmi Bolat, Hilal Aydın, Dilan Genç-Akdağ

|Dec 12, 2025
Novel RORA Variants Reveal Genotype-Phenotype Diversity and Variable Expressivity in Neurodevelopmental Disorders.

Gul Unsel-Bolat, Hilmi Bolat, Senol Citli

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Frequent Collaborators

8 joint publications

Hilmi Bolat

1 joint publications

Zehra Manav Yiğit

1 joint publications

Aydan Mengübaş Erbaş

1 joint publications

Ayberk Türkyılmaz