Merve Koç Yekedüz

Ankara University — Turkey

Biochemistry, Genetics and Molecular Biology · Life Sciences

6h-index78citations39works0.42yr avg
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Research Topics

Metabolism and Genetic Disorders(15), Lysosomal Storage Disorders Research(7), Folate and B Vitamins Research(5), Cellular transport and secretion(4), Parkinson's Disease Mechanisms and Treatments(3)

Publications39 total

Dual-Risk axis: <i>GBA1</i> mutations and occupational pesticide exposure in Parkinson's disease
Journal of Parkinson s Disease·2026Open Access
When It’s Not Phenylketonuria: Alternative Diagnoses Revealed by Newborn Screening for Hyperphenylalaninemia
Turkish Archives of Pediatrics·2025Open Access
Carboxypeptidase D deficiency causes hearing loss amenable to treatment
Journal of Clinical Investigation·2025Open Access
A Multinational Study of Patient and Caregiver‐Reported Insights Into <scp>ADSS1</scp> Myopathy
Muscle & Nerve·2025· 1 cited
NOD-m: a novel clinical score for predicting hearing loss in inherited metabolic disorders
European Archives of Oto-Rhino-Laryngology·2025Open Access
Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor
Neurological Sciences·2025· 1 citedOpen Access
Enhancing clinical decision-making: a scenario-based patient simulation study using QR code-based algorithms for the management of acute intoxication-type inborn errors of metabolism
The Turkish Journal of Pediatrics·2025Open Access
Canpolat&amp;Karaman&amp;Kardaş - Temel Pediatrik Nöroradyoloji Nörometabolik ve Heredodejeneratif Hastalıklarda Klinik ve Radyolojik Yaklaşım
2025Open Access
Reduced Cerebellar Volumes Associate with P300 Amplitude Attenuation in Children with Clinical High Risk for Psychosis and Early Onset Psychosis
The Cerebellum·2025
Retrospective assessment of hepatic involvement in patients with inherited metabolic disorders: nine-year single-center experience
Journal of Pediatric Endocrinology and Metabolism·2025Open Access
Çocuk ve Ergenlerde Beyin Gelişimi ve Beyin Gelişimini Etkileyen Faktörler
2025Open Access
Challenges Faced by Newborns with Inherited Metabolic Disorders and Their Mothers During Antepartum, Intrapartum, and Postpartum Periods
Fetal and Pediatric Pathology·2025
Evaluation of scientific validity and appropriateness of artificial intelligence-assisted ChatGPT advices in dietary treatment of methylmalonic acidemia
Nutrición Hospitalaria·2025Open Access
Fronto-Cerebellar Features Associate with Cognitive Dysfunction in Childhood-Onset Systemic Lupus Erythematosus
SSRN Electronic Journal·2025Open Access
Quality of Life and Related Factors in Patients Diagnosed with Mucopolysaccharidosis and Their Caregivers
Klinische Pädiatrie·2024· 1 cited
Scale consistance in cognitive status awareness of patients with Parkinson’s disease
Turkish Journal Of Neurology·2024Open Access
Diagnosis and Treatment of Newborns Referred to the Metabolism Department From the National Newborn Screening Program in Türkiye: A 5-Year Single-Center Experience
Turkish Journal of Pediatric Disease·2024· 2 citedOpen Access
Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis?
Pediatric Neurology·2024· 1 cited
Türkiye’s First Multidisciplinary Gene Therapy Education Program: History and Plans for the Future
Journal of Contemporary Medicine·2024· 1 citedOpen Access
Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review
Journal of Pediatric Endocrinology and Metabolism·2024· 1 cited
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Frequent Co-authors

Fatma Tuba Eminoğlu(31), Engi̇n Köse(20), Neslihan Doğulu(10), Ümmühan Öncül(10), İlknur Sürücü Kara(6), Talha Abalı(4), Muhittin Cenk Akbostancı(4), Rezzak Yılmaz(4), Ahmet Veli Karacan(3), Sema Nur Kibrit(3), Elif Yüsra Unutmaz(3), Serdar Ceylaner(3), Hanne van der Heijden(3), Jaymin Upadhyay(3), Fatma Ceren Sarıoğlu(3), Görkem Kayiş(2), Zeynep Şıklar(2), Emel Okulu(2), Ömer Erdeve(2), Saadet Arsan(2)