Dr. Öğr. Üyesi Mutluay ARSLAN

1. Neurological complications of rotavirus infection in pediatric patients: a retrospective cohort study

Bilgin N., ARSLAN M., TEKİN K., Baştemur M., ÜNAY B.

Acta Neurologica Belgica , cilt.126, sa.4, ss.1355-1363, 2026 (SCI-Expanded, Scopus)

2. Diagnostic value of machine-learning using conventional magnetic resonance imaging markers for pediatric idiopathic intracranial hypertension: a retrospective study

CÜCE F., Tulum G., Işık M. I., Baştemur M., ARSLAN M., ÜNAY B., et al.

Pediatric Radiology , cilt.56, sa.7, ss.1516-1535, 2026 (SCI-Expanded, Scopus)

3. Clinical diversity of different genetic variants changes the way we look at diseases; Two cases of ACTL6B gene-related DECAM syndrome

Üstün C., Coşkun A. N., ARSLAN M., TORUN D., ÜNAY B.

Neurology Asia , cilt.31, sa.2, ss.847-851, 2026 (SCI-Expanded, Scopus)

4. Oligogenic inheritance in epilepsy: A systematic exome-wide analysis

Gravel B., Soblet J., Legros B., Santos S. F., Van Paesschen W., Rikir E., et al.

Epilepsia , 2026 (SCI-Expanded, Scopus)

5. Clinical Characteristics and EEG Findings of Patients with Childhood Absence Epilepsy Çocukluk Çağı Absans Epilepsili Hastaların Klinik Özellikleri ve EEG Bulguları

Baştemur M., Yalçın H. N., Bilgin N., ARSLAN M., ÜNAY B.

Genel Tip Dergisi , cilt.35, sa.6, ss.1178-1189, 2025 (Scopus, TRDizin)

6. Evaluation of resilience in pediatric well-controlled epilepsy patients

ARSLAN M., Coşkun A. N., Üstün C., Hür Ö., ÜNAY B.

Clinical Neurology and Neurosurgery , cilt.249, 2025 (SCI-Expanded, Scopus)

7. Can serum orexin levels be used as a marker in childhood epilepsy?

ARSLAN M., Üstün C., Coşkun A. N., Çelik H., Yalçın H. N., KARAİSMAİLOĞLU E., et al.

Heliyon , cilt.11, sa.1, 2025 (SCI-Expanded, Scopus)

8. Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study

Kanmaz S., Tekgul H., Kayilioglu H., Atas Y., Kart P. O., Yildiz N., et al.

Seizure , cilt.123, ss.17-25, 2024 (SCI-Expanded, Scopus)

9. Screening for creatine transporter deficiency in autism spectrum disorder: a pilot study

ARSLAN M., YILDIZ Y., Olgaç A., Hekim Ö., YÜCEL Ç., SERTOĞLU E.

Turkish Journal of Biochemistry , cilt.49, sa.6, ss.784-791, 2024 (SCI-Expanded, Scopus, TRDizin)

10. Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Berkovic S. F., Neale B. M., Zsurka G., Zizovic M., Zimprich F., Zara F., et al.

Nature Neuroscience , cilt.27, sa.10, ss.1864-1879, 2024 (SCI-Expanded, Scopus)

11. Effectiveness of Peripheral Nerve Block in Terms of Search for a Standardized Treatment Protocol in Diabetic Foot Patients Using Anticoagulants A Double-Center Study

ÖZKAN D. B., ARSLAN M., EŞKİN M. B., Sipahioglu F. O., Ermis Y., ÖZKAN G., et al.

Journal of the American Podiatric Medical Association , cilt.114, sa.2, 2024 (SCI-Expanded, Scopus)

12. Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Montanucci L., Collins R. L., Niestroj L., Parthasarathy S., Xian J., Ganesan S., et al.

Nature Communications , cilt.14, sa.1, 2023 (SCI-Expanded, Scopus)

13. POU3F3-related disorder: Defining the phenotype and expanding the molecular spectrum

Rossi A., Blok L. S., Neuser S., Klöckner C., Platzer K., Faivre L. O., et al.

Clinical Genetics , cilt.104, sa.2, ss.186-197, 2023 (SCI-Expanded, Scopus)

14. Preliminary evaluation of potential urinary organic acid biomarkers with mass spectrometry in children with autism spectrum disorder

SERTOĞLU E., Balik A. R., Duman U. G., Mavis M. E., ARSLAN M., YILDIZ Y., et al.

Research in Autism Spectrum Disorders , cilt.106, 2023 (SSCI, Scopus)

15. Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes

YILMAZ Ü., Gücüyener K., Yavuz M., Öncel İ., CANPOLAT M., ÜNVER O., et al.

European Journal of Paediatric Neurology , cilt.41, ss.8-18, 2022 (SCI-Expanded, Scopus)

16. THE EVALUATION OF PHYSICAL ACTIVITY AND PHYSICAL FITNESS LEVELS IN ADOLESCENT INDIVIDUALS WITH CEREBRAL PALSY Adölesan Serebral Palsili Bireylerde Fiziksel Aktivite ve Fiziksel Uygunluk Seviyelerinin Değerlendirilmesi

Erol H., Sertel M., Alpcan A., ARSLAN M.

Journal of Kirikkale University Faculty of Medicine , cilt.24, sa.1, ss.73-82, 2022 (Scopus, TRDizin)

17. Clinical Heterogeneity in MT-ATP6 Pathogenic Variants: Same Genotype—Different Onset

Capiau S., Smet J., De Paepe B., YILDIZ Y., ARSLAN M., Stevens O., et al.

Cells , cilt.11, sa.3, 2022 (SCI-Expanded, Scopus)

18. Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome

TORUN D., ARSLAN M., Çavdarlı B., Akar H., Cram D. S.

Turkish Journal of Pediatrics , cilt.64, sa.5, ss.956-963, 2022 (SCI-Expanded, Scopus, TRDizin)

19. Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature

Ceylan A. C., Acar Arslan E., ERDEM H. B., Kavus H., ARSLAN M., Topaloğlu H.

Acta Neurologica Belgica , cilt.121, sa.6, ss.1457-1462, 2021 (SCI-Expanded, Scopus)

20. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

Koko M., Krause R., Sander T., Bobbili D. R., Nothnagel M., May P., et al.

eBioMedicine , cilt.72, 2021 (SCI-Expanded, Scopus)

21. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

Motelow J. E., Povysil G., Dhindsa R. S., Stanley K. E., Allen A. S., Feng Y. A., et al.

American Journal of Human Genetics , cilt.108, sa.6, ss.965-982, 2021 (SCI-Expanded, Scopus)

22. Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok-Fisher syndrome suggests the presence of a POU3F3-related SNIBFIS endophenotype: A case report

TORUN D., ARSLAN M., Yüksel Z.

American Journal of Medical Genetics, Part A , cilt.185, sa.5, ss.1554-1560, 2021 (SCI-Expanded, Scopus)

23. The relationship of motor development with sensory processing among infants born very preterm: A prospective case-control study

Kara Ö. K., ŞAHİN S., TONAK H. A., ARSLAN M., KÖSE B., KARA K.

Turkish Journal of Pediatrics , cilt.63, sa.5, ss.855-866, 2021 (SCI-Expanded, Scopus)

24. A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome

Mısırlıgil M., YILDIZ Y., AKIN O., Güneş S. O., ARSLAN M., ÜNAY B.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.4, ss.452-455, 2021 (SCI-Expanded, Scopus, TRDizin)

25. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17458 subjects

Niestroj L., Perez-Palma E., Howrigan D. P., Zhou Y., Cheng F., Saarentaus E., et al.

Brain , cilt.143, sa.7, ss.2106-2118, 2020 (SCI-Expanded, Scopus)

26. Genotypes and estimated prevalence of phosphomannomutase 2 deficiency in Turkey differ significantly from those in Europe

YILDIZ Y., ARSLAN M., Çelik G., Kasapkara Ç. S., CEYLANER S., DURSUN A., et al.

American Journal of Medical Genetics, Part A , cilt.182, sa.4, ss.705-712, 2020 (SCI-Expanded, Scopus)

27. Neuromotor and sensory development in preterm infants: Prospective study Yenidoğan preterm bebeklerde nöromotor ve duyusal gelişim: Prospektif çalışma

Kara Ö. K., ŞAHİN S., KARA K., ARSLAN M.

Turkish Archives of Pediatrics , cilt.55, sa.1, ss.46-53, 2020 (ESCI, Scopus, TRDizin)

28. Polygenic burden in focal and generalized epilepsies

Leu C., Stevelink R., Smith A. W., Goleva S. B., Kanai M., Ferguson L., et al.

Brain , cilt.142, sa.11, ss.3473-3481, 2019 (SCI-Expanded, Scopus)

29. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Feng Y. A., Howrigan D. P., Abbott L. E., Tashman K., Cerrato F., Singh T., et al.

American Journal of Human Genetics , cilt.105, sa.2, ss.267-282, 2019 (SCI-Expanded, Scopus)

30. Hypertrophic Neuropathy of the Sciatic Nerve

YİŞ U., ARSLAN M., GÜLERYÜZ UÇAR H.

Pediatric Neurology , cilt.87, ss.77, 2018 (SCI-Expanded, Scopus)

31. A multicenter cross-sectional study to evaluate the clinical characteristics and nutritional status of children with cerebral palsy

Aydin K., Aydin K., Akbas Y., ÜNAY B., ARSLAN M., CANSU A., et al.

Clinical Nutrition ESPEN , cilt.26, ss.27-34, 2018 (Scopus)

32. Perinatal risk factors for asthma in children with allergic rhinitis and grass pollen sensitization

Yavuz S. T., Siebert S., Akin O., ARSLAN M., Civelek E., Bagci S.

Allergy and Asthma Proceedings , cilt.39, sa.3, 2018 (SCI-Expanded, Scopus)

33. Evaluation of somatosensory evoked potentials (SEPs) in obese children

Akin O., ÜNAY B., ARSLAN M., Mazman S., Taşçilar E., Eker I.

Gulhane Medical Journal , cilt.60, sa.1, ss.5-8, 2018 (Scopus, TRDizin)

34. Basics of bone metabolism and osteoporosis in common pediatric neuromuscular disabilities

YAŞAR E., Adigüzel E., ARSLAN M., Matthews D. J.

European Journal of Paediatric Neurology , cilt.22, sa.1, ss.17-26, 2018 (SCI-Expanded, Scopus)

35. Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

YILMAZ Ü., Anlar B., Gücüyener K., Yaramış A., CANSU A., ÜNALP A., et al.

European Journal of Paediatric Neurology , cilt.21, sa.6, ss.864-872, 2017 (SCI-Expanded, Scopus)

36. Relation of insulin resistance to neurocognitive function and electroencephalography in obese children

Akin O., Eker I., ARSLAN M., Yavuz S. T., Akman S., Taşçllar M. E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.30, sa.10, ss.1027-1032, 2017 (SCI-Expanded, Scopus)

37. Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies

Masnada S., Hedrich U. B., Gardella E., Schubert J., Kaiwar C., Klee E. W., et al.

Brain , cilt.140, sa.9, ss.2337-2354, 2017 (SCI-Expanded, Scopus)

38. Association of neck circumference and pulmonary function in children

Akın O., ARSLAN M., HAYMANA C., KARABULUT E., Hacihamdioglu B., Yavuz S. T.

Annals of Allergy, Asthma and Immunology , cilt.119, sa.1, ss.27-30, 2017 (SCI-Expanded, Scopus)

39. Association of nerve conduction impairment and insulin resistance in children with obesity

Akın O., Eker İ., ARSLAN M., Taşdemir S., Taşçılar M. E., Ulaş Ü. H., et al.

Child's Nervous System , cilt.32, sa.11, ss.2219-2224, 2016 (SCI-Expanded, Scopus)

40. SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations

Usluer S., Salar S., ARSLAN M., YİŞ U., KARA B., Tektürk P., et al.

Seizure , cilt.39, ss.34-43, 2016 (SCI-Expanded, Scopus)

41. Association of wider neck circumference and asthma in obese children

Akin O., Sari E., ARSLAN M., Yeşilkaya E., Hacihamdioglu B., Yavuz S. T.

Annals of Allergy, Asthma and Immunology , cilt.116, sa.6, ss.514-517, 2016 (SCI-Expanded, Scopus)

42. Evaluation of plasma melatonin levels in children with afebrile and febrile seizures

Dabak O., Altun D., ARSLAN M., Yaman H., VURUCU S., Yesilkaya E., et al.

Pediatric Neurology , cilt.57, ss.51-55, 2016 (SCI-Expanded, Scopus)

43. Visual and brainstem auditory evoked potentials in children with obesity

Akin O., ARSLAN M., Akgün H., Yavuz S. T., Sari E., Taşçilar M. E., et al.

Brain and Development , cilt.38, sa.3, ss.310-316, 2016 (SCI-Expanded, Scopus)

44. Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-mb deletion of 14q12 q21.2 and a 550-kb deletion of 18p11.23: Microarray delineation of an unbalanced chromosome rearrangement and a literature review

TORUN D., ARSLAN M., Akar H., Karaer K., ÜNAY B., TUNCA Y.

Genetic Counseling , cilt.27, sa.2, ss.165-176, 2016 (SCI-Expanded, Scopus)

45. A rare complication of wasp sting: acute cervical dystonia

ARSLAN M., GÜNGÖR A., Akın O., ÜNAY B., Yavuz S. T.

Child's Nervous System , cilt.31, sa.12, ss.2213-2214, 2015 (SCI-Expanded, Scopus)

46. Is there any difference between high-risk infants with different birth weight and gestational age in neurodevelopmental characters? Farklı doğum ağırlığı ve gebelik yaşına sahip yüksek riskli bebeklerin nörogelişimsel özellikleri arasında fark var mıdır?

Kara Ö. K., KEREM GÜNEL M., Açıkel C., Yiğit Ş., ARSLAN M.

Turk Pediatri Arsivi , cilt.50, sa.3, ss.151-157, 2015 (Scopus, TRDizin)

47. KIAA0586 is Mutated in Joubert Syndrome

Bachmann-Gagescu R., Phelps I. G., Dempsey J. C., Sharma V. A., Ishak G. E., Boyle E. A., et al.

Human Mutation , cilt.36, sa.9, ss.831-835, 2015 (SCI-Expanded, Scopus)

48. Wider neck circumference is related to severe asthma in children

Hacihamdioglu B., ARSLAN M., Yeşilkaya E., Gok F., Yavuz S. T.

Pediatric Allergy and Immunology , cilt.26, sa.5, ss.456-460, 2015 (SCI-Expanded, Scopus)

49. De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Syrbe S., Hedrich U. B., Riesch E., Djémié T., Müller S., Møller R. S., et al.

Nature Genetics , cilt.47, sa.4, ss.393-399, 2015 (SCI-Expanded, Scopus)

50. Stevens-johnson syndrome triggered by a combination of clobazam, lamotrigine and valproic acid in a 7-year-old child

Yapici A. K., Fidanci M., Kilic S., Balamtekin N., ARSLAN M., Yavuz S., et al.

Annals of Burns and Fire Disasters , cilt.27, sa.3, ss.121-125, 2014 (Scopus)

51. Brachydactyly mental retardation syndrome in differential diagnosis of pseudopseudohypoparathyroidism

Hacihamdioǎlu B., ARSLAN M., Sari E., Kurtçu K., Yesilkaya E.

Journal of Pediatric Endocrinology and Metabolism , cilt.26, sa.7-8, ss.793-795, 2013 (SCI-Expanded, Scopus)

52. A novel mutation in the sodium channel α1 subunit gene in a child with dravet syndrome in Turkey

ARSLAN M., YİŞ U., Çaǧlayan H., Akin R.

Neural Regeneration Research , cilt.8, sa.10, ss.955-958, 2013 (SCI-Expanded, Scopus)

53. Ring chromosome 21 in the differential diagnosis of waddling gait

ARSLAN M., YİŞ U., VURUCU S., TUNCA Y., ÜNAY B., Akin R.

Brain and Development , cilt.34, sa.9, ss.792-795, 2012 (SCI-Expanded, Scopus)

54. Acquired epileptiform opercular syndrome: F-18 fluorodeoxyglucose positron emission tomography (FDG-PET) findings and efficacy of levetiracetam therapy

ARSLAN M., YİŞ U., VURUCU S., İNCE S., ÜNAY B., Akin R.

Epilepsy and Behavior , cilt.25, sa.1, ss.50-53, 2012 (SCI-Expanded, Scopus)

55. The effects of biotin supplementation on serum and liver tissue biotinidase enzyme activity and alopecia in rats which were administrated to valproic acid

ARSLAN M., VURUCU S., Balamtekin N., ÜNAY B., Akin R., Kurt I., et al.

Brain and Development , cilt.31, sa.6, ss.405-410, 2009 (SCI-Expanded, Scopus)

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Yayın (WoS)

Yayın (Scopus)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Atıf (TrDizin)

H-İndeks (TrDizin)

Atıf (Diğer Toplam)

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