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Akademisyen

HİLMİ BOLAT

DOÇENT

BALIKESİR ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Tıbbi Genetik

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 75
  • Proje 0
  • Kitap 0
  • Bildiri 0
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 14 Q2 27 Q3 21 Q4 6
WoS (JCR) Q1 8 Q2 8 Q3 23 Q4 26
TR Index 12 makale

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

Üst %1 makale 0
Üst %10 makale 4
Ort. yüzdelik 50.6%
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 75 yayın

Scopus (SJR)
Q1 14 Q2 27 Q3 21 Q4 6
WoS (JCR)
Q1 8 Q2 8 Q3 23 Q4 26
TR Index
12 makale

Makale listesi

  1. 2026 Circulating miR-221/222 and Serum IL-23 in Treatment-Naïve Multiple Sclerosis: A Case–Control Study Medicina DOI 10.3390/medicina62081468 YÖKSİS SJR Q2 JCR Q1 OpenAlex 69.4%
  2. 2026 Symptom-Based Classification of 16p11. 2 Copy Number Variations Underlying the Multidimensional Autism Spectrum Disorder Phenotype Using Machine Learning Methods Research in Autism DOI 10.1016/j.reia.2026.202865 YÖKSİS SJR Q2 OpenAlex 13.7%
  3. 2026 OTUD5-related rare X-linked multiple congenital anomalies and neurodevelopmental syndrome: clinical findings and review of the literature Neurogenetics DOI 10.1007/s10048-026-00896-1 YÖKSİS SJR Q3 JCR Q4 OpenAlex 20.2%
  4. 2026 Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition Neurological Sciences DOI 10.1007/s10072-026-08883-y YÖKSİS SJR Q1 JCR Q3 OpenAlex 13.7%
  5. 2026 TRMT10A‐Related Neurodevelopmental Disorder Without Metabolic Findings Human Mutation DOI 10.1155/humu/8058409 YÖKSİS SJR Q1 JCR Q4 OpenAlex 46.0%
  6. 2026 Testing DAT1 and DRD4 Genes in Attention Deficit Hyperactivity Disorder Using a Wide Spectrum of Neurocognitive Batteries and DRD4 Genes in Attention Deficit Hyperactivity Disorder Using a Wide Spectrum of Neurocognitive Batteries International Journal of Developmental Neuroscience DOI 10.1002/jdn.70133 YÖKSİS SJR Q3 JCR Q4 OpenAlex 42.5%
  7. 2026 A novel compound heterozygous YY1AP1 variant in Grange syndrome: importance of early signs in preventing life-threatening vascular complications Journal of Human Genetics DOI 10.1038/s10038-026-01471-0 YÖKSİS SJR Q2 JCR Q3 OpenAlex 25.4%
  8. 2026 ATP6V0A2-Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.70102 YÖKSİS SJR Q2 JCR Q4 OpenAlex 14.6%
  9. 2026 Epigenetic regulators and inflammation antagonists in familial Mediterranean fever: the role of hsa-miR-335-5p, hsa-miR-26b-5p, hsa-miR-16-5p miRNAs and IL-36Ra levels in pathogenesis Immunologic Research DOI 10.1007/s12026-026-09771-5 YÖKSİS SJR Q3 JCR Q3 OpenAlex 27.8%
  10. 2026 Relationship between BDNF rs6265 (VAL66MET) polymorphism and serum BDNF LEVELS in anxiety disorders Molecular Biology Reports DOI 10.1007/s11033-026-12395-5 YÖKSİS SJR Q2 JCR Q3 OpenAlex 72.8%
  11. 2026 Rare Variants in Purinergic P2X Receptor Genes (P2RX4, P2RX5, P2RX7) in Individuals With Autism Spectrum Disorder: An Exploratory Study Human Mutation DOI 10.1155/humu/5522396 YÖKSİS SJR Q1 JCR Q4 OpenAlex 72.5%
  12. 2026 ATP6V0A2 ‐Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.70102 YÖKSİS SJR Q2 JCR Q4 OpenAlex 14.6%
  13. 2026 Multimodal Imaging and Electrophysiological Features of Genetically Confirmed Inherited Retinal Dystrophies Balıkesır Health Sciences Journal DOI 10.53424/balikesirsbd.1757960 YÖKSİS TR Index OpenAlex 15.6%
  14. 2025 Relationship between symptom severity, glutamate levels, and N-methyl-D-aspartate receptor target microRNA expression in patients with panic disorder Psychiatric Genetics DOI 10.1097/YPG.0000000000000402 YÖKSİS SJR Q3 JCR Q4 OpenAlex 24.9%
  15. 2025 Could Transforming Growth Factor Beta and Target MicroRNA Dysregulation Serve as Biomarkers of Symptom Severity in Patients With Obsessive‐Compulsive Disorder? International Journal of Developmental Neuroscience DOI 10.1002/jdn.70070 YÖKSİS SJR Q3 JCR Q4 OpenAlex 84.0%
  16. 2025 Clinical and Genetic Characteristics of Patients with Essential Tremor Who Develop Parkinson’s Disease Medicina DOI 10.3390/medicina61071184 YÖKSİS SJR Q2 JCR Q1 OpenAlex 19.4%
  17. 2025 Clinical Insights Into a Rare SETD2 Disorder: Report of a Novel Variant Developmental Neurobiology DOI 10.1002/dneu.70002 YÖKSİS SJR Q2 JCR Q3 OpenAlex 64.1%
  18. 2025 Genetic Syndromes Including Intellectual Disability and Different Cancer Types Molecular Syndromology DOI 10.1159/000549291 YÖKSİS SJR Q3 JCR Q4 OpenAlex 25.4%
  19. 2025 EMC10 Gene Variants May Cause Dual Molecular Effects on the Neuropsychiatric Disease Pattern Developmental Neurobiology DOI 10.1002/dneu.22994 YÖKSİS SJR Q2 JCR Q3 OpenAlex 76.5%
  20. 2025 Novel RORA Variants Reveal Genotype-Phenotype Diversity and Variable Expressivity in Neurodevelopmental Disorders Clinical Genetics DOI 10.1111/cge.70120 YÖKSİS SJR Q2 JCR Q3 OpenAlex 65.2%

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