Nejmiye Akkuş

5PUBLICATIONS
6CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Predictive and prognostic markersGene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)
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Publications (5)

|Jan 08, 2026
Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A-Related Intellectual Disability.

Nejmiye Akkus, Abdullah Canbal, Seda Guneysu

|Mar 28, 2025
Unveiling the role of miRNA in laryngeal squamous cell carcinoma progression: a retrospective study.

Nejmiye Akkuş, Elif Kaya Çelik, Suleyman Ozdemir

|Mar 10, 2025
Glutathione S-transferase polymorphisms and their role in recurrent pregnancy loss: A genetic risk assessment.

Nejmiye Akkus, Hande Kucuk Kurtulgan

|Apr 25, 2024
Diagnostic yield of the chromosomal microarray analysis in turkish patients with unexplained development delay/ıntellectual disability(ID), autism spectrum disorders and/or multiple congenital anomalies and new clinical findings.

Nejmiye Akkus, Pelin Ozyavuz Cubuk

|Aug 14, 2023
First Clinical Report of Two RAB3GAP1 Pathogenic Variant in Warburg Micro Syndrome.

Nejmiye Akkuş, Tuğba Akın Duman

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Frequent Collaborators

1 joint publications

Pelin Ozyavuz Cubuk

1 joint publications

Hande Kucuk Kurtulgan

1 joint publications

Elif Kaya Çelik

1 joint publications

Suleyman Ozdemir