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akaturk Akademik ölçüm

Akademisyen

MERVE KOÇ YEKEDÜZ

ÖĞRETİM GÖREVLİSİ

ANKARA ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk Metabolizma Hastalıkları (Çocuk Sağlığı ve Hastalıkları)

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 52
  • Proje 0
  • Kitap 0
  • Bildiri 99
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 12 Q2 12 Q3 11 Q4 3
WoS (JCR) Q1 6 Q2 6 Q3 18 Q4 8
TR Index 11 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 0
Üst %10 makale 3
Ort. yüzdelik 47.3%
Üst %1 payı 0.0%
Üst %10 payı 5.6%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 52 yayın

Makale listesi

  1. 2026 Personalized Low Protein Products Produced with a 3D Food Printer for Inherited Metabolic Diseases on Restricted Diet Annals of Nutrition and Metabolism DOI 10.1159/000550101 YÖKSİS SJR Q2 JCR Q3 OpenAlex 2.9%
  2. 2026 Dual-Risk axis: GBA1 mutations and occupational pesticide exposure in Parkinson's disease JOURNAL OF PARKINSONS DISEASE DOI 10.1177/1877718X251412233 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 91.5%
  3. 2025 Retrospective assessment of hepatic involvement in patients with inherited metabolic disorders: nine-year single-center experience. Journal of pediatric endocrinology & metabolism : JPEM DOI 10.1515/jpem-2024-0511 YÖKSİS SJR Q3 JCR Q3 OpenAlex 4.0%
  4. 2025 Challenges Faced by Newborns with Inherited Metabolic Disorders and Their Mothers During Antepartum, Intrapartum, and Postpartum Periods. Fetal and pediatric pathology DOI 10.1080/15513815.2024.2447082 YÖKSİS SJR Q3 JCR Q4 OpenAlex 66.0%
  5. 2025 Carboxypeptidase D deficiency causes hearing loss amenable to treatment Journal of Clinical Investigation DOI 10.1172/JCI192090. YÖKSİS SJR Q1 JCR Q1 OpenAlex 69.7%
  6. 2025 NOD-m: a novel clinical score for predicting hearing loss in inherited metabolic disorders. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery DOI 10.1007/s00405-025-09477-8 YÖKSİS SJR Q1 JCR Q1 OpenAlex 14.6%
  7. 2025 Evaluation of scientific validity and appropriateness of artificial intelligence-assisted ChatGPT advices in dietary treatment of methylmalonic acidemia Nutrición Hospitalaria DOI 10.20960/nh.06026 YÖKSİS SJR Q3 JCR Q4 OpenAlex 24.1%
  8. 2025 Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology DOI 10.1007/s10072-025-08286-5 YÖKSİS SJR Q1 JCR Q3 OpenAlex 78.4%
  9. 2025 Reduced Cerebellar Volumes Associate with P300 Amplitude Attenuation in Children with Clinical High Risk for Psychosis and Early Onset Psychosis The Cerebellum DOI 10.1007/s12311-025-01822-1 YÖKSİS SJR Q1 JCR Q3 OpenAlex 66.8%
  10. 2025 A Multinational Study of Patient and Caregiver‐Reported Insights Into ADSS1 Myopathy Muscle & Nerve DOI 10.1002/mus.70033 YÖKSİS SJR Q1 JCR Q2 OpenAlex 71.9%
  11. 2024 Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis? Pediatric Neurology DOI 10.1016/j.pediatrneurol.2024.03.032 YÖKSİS SJR Q1 JCR Q2 OpenAlex 61.7%
  12. 2024 Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2023-0490 YÖKSİS SJR Q2 JCR Q3 OpenAlex 45.5%
  13. 2024 Quality of Life and Related Factors in Patients Diagnosed with Mucopolysaccharidosis and Their Caregivers Klinische Pädiatrie DOI 10.1055/a-2451-6562 YÖKSİS SJR Q3 JCR Q3 OpenAlex 66.4%
  14. 2024 Scale consistance in cognitive status awareness of patients with Parkinson’s disease Turkish Journal of Neurology DOI 10.55697/tnd.2024.139 YÖKSİS TR Index OpenAlex 15.1%
  15. 2024 Türkiye’s First Multidisciplinary Gene Therapy Education Program: History and Plans for the Future Journal of Contemporary Medicine DOI 10.16899/jcm.1446436 YÖKSİS OpenAlex 34.1%
  16. 2023 A different approach to the evaluation of the genotype-phenotype relationship in biotinidase deficiency: repeated measurement of biotinidase enzyme activity J Pediatr Endocrinol Metab. DOI 10.1515/jpem-2023-0337 YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.8%
  17. 2023 Cross-Cultural Differences in Stigma Associated with Parkinson’s Disease: A Systematic Review IOS Press DOI 10.3233/JPD-230050 YÖKSİS SJR Q1 JCR Q2 OpenAlex 81.3%
  18. 2023 IGAm: A novel index predicting long-term survival in patients with early-diagnosed inherited metabolic disorders J Pediatr Endocrinol Metab . DOI 10.1515/jpem-2023-0272 YÖKSİS SJR Q2 JCR Q3 OpenAlex 17.3%
  19. 2023 A Cause of Refractory Seizures: Fumarase Deficiency Journal of Pediatric Neurosciences DOI 10.4103/jpn.JPN_105_21 YÖKSİS SJR Q3 JCR Q4 OpenAlex 25.3%
  20. 2023 Kalıtsal Metabolik Hastalıkların Tedavisinde Sekonder Uygulama Alanı Olarak Ketojenik Diyet Tedavisi: Nonketotik Hiperglisinemili Bir Olgu Sunumu Bes Diy Derg Turkish Dietetic Association Partner DOI 10.33076/2023.BDD.1736 YÖKSİS TR Index OpenAlex 6.2%

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