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Psychiatry and Clinical Psychopharmacology|May 20, 2024
Peripheral Expression of MACROD2 Gene Is Reduced Among a Sample of Turkish Children with Autism Spectrum DisorderAlper Alnak, İpek Kuşcu Özücer, Ahmet Okay Çağlayan, et al.
The Turkish Journal of Pediatrics|December 30, 2022
Familial clustering of nasopharyngeal carcinoma in the family of an adolescent with nasopharyngeal carcinomaBuket Kara, Kübra Ertan, Mürsel Düzova, et al.
The Turkish Journal of Pediatrics|December 30, 2022
Cerebral developmental venous anomalies in children with mismatch repair deficiencyBuket Kara, Yahya Paksoy, Ahmet Okay Çağlayan, et al.
Psychiatry and Clinical Psychopharmacology|May 20, 2024
Peripheral Expression of ADORA2A Is Increased and Is Correlated with Autism Spectrum Disorder Severity in a Sample of Turkish ChildrenHilal Akköprü, Alper Alnak, Zeynep Nur Karadoğan, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 10, 2025
Rare Genetic Variants of Cell Adhesion Molecules in Transgender Men Suggest a Potential Role in Gender DysphoriaDuygu Onur Cura, Tufan Çankaya, Özden Altiok Clark, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 7, 2023
Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single centerMehmet Kocabey, Hande Özkalaycı, Tufan Çankaya, et al.
European Journal of Ophthalmology|May 12, 2021
Analysis of genotype-phenotype correlation in Walker-Warburg syndrome with a novel CRPPA mutation in different clinical manifestationsNurettin Bayram, Ayşe Kaçar Bayram, Hüseyin Per, et al.
Neuropediatrics|August 13, 2015
The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency SyndromeHakan Gumus, Ayşe Kaçar Bayram, Fatih Kardas, et al.
American Journal of Medical Genetics. Part A|March 15, 2023
An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variantAylin Yüksel Ülker, Dilek Uludağ Alkaya, Ahmet Okay Çağlayan, et al.
The Turkish Journal of Pediatrics|March 9, 2021
Nasopharyngeal carcinoma in a child with Kartagener`s syndromeBuket Kara, Nusret Seher, Meryem İlkay Eren-Karanis, et al.
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