Nihan Hande Akçakaya

6PUBLICATIONS
16CO-AUTHORS
Behavioural neuroscienceInfant and child healthEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesMedical infection agents (incl. prions)
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Publications (6)

|Nov 25, 2025
Missense variants in PKAN: insights from a multi-patient genetic analysis.

Melisa Kılıç, Sevcan Mercan, Banu Özen Barut

|Jul 21, 2025
Medicolegal evaluation of pediatric patients with injection neuropathy.

Hızır Asliyüksek, Caner Beşkoç, Ömer Faruk Şimşeker

|Nov 13, 2022
Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.

Sevcan Mercan, Nihan Hande Akcakaya, Baris Salman

|Apr 04, 2020
Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey.

Nihan H Akçakaya, Burçak Özeş Ak, Michael A Gonzalez

|Dec 06, 2019
Clinical and genetic spectrum of an orphan disease MPAN: a series with new variants and a novel phenotype.

Nihan Hande Akçakaya, Garen Haryanyan, Sevcan Mercan

|Jan 07, 2019
A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analysis.

Nihan Hande Akçakaya, Barış Salman, Zeliha Görmez

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Frequent Collaborators

2 joint publications

Sibel Aylin Ugur Iseri

1 joint publications

Baris Salman

1 joint publications

Ugur Ozbek

1 joint publications

Hızır Asliyüksek