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Dilan Genç-Akdağ

Observed names: Dilan Genç Akdağ, Dilan Genç‐Akdağ, Genç Akdağ, Dilan
Observed institution: Balıkesir University
OpenAlex ID: A5126422901
EMC10 Gene Variants May Cause Dual Molecular Effects on the Neuropsychiatric Disease Pattern
2025 · Hilmi Bolat, Dilan Genç Akdağ, et al. · Developmental Neurobiology · 1
A novel compound heterozygous YY1AP1 variant in Grange syndrome: importance of early signs in preventing life-threatening vascular complications
2026 · Gul Unsel-Bolat, Neslihan Tezcan, et al. · Journal of Human Genetics
OTUD5-related rare X-linked multiple congenital anomalies and neurodevelopmental syndrome: clinical findings and review of the literature
2026 · Arzu Eroğlu, Dilan Genç Akdağ, et al. · Neurogenetics
Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition
2026 · Hilmi Bolat, Hilal Aydın, et al. · Neurological Sciences
Clinical Insights Into a Rare SETD2 Disorder: Report of a Novel Variant
2025 · Gül Ünsel‐Bolat, Dilan Genç‐Akdağ, et al. · Developmental Neurobiology
Prevalence of Fragile X Syndrome in Neurodevelopmental Disorders: A Single-Center Experience
2025 · Ünsel-bolat, Gül, Sönmez, Demirkan, et al. · Harran Üniversitesi Tıp Fakültesi Dergisi
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Spectrum of BRCA1 and BRCA2 Variants in Breast Cancer Cases: A Single-Center Experience
2025 · Esener, Zeynep, Saray, Seray, et al. · Balıkesır Health Sciences Journal
Works count: 7
Citation count: 1
H-index: 1
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