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Academician

ZÜHAL YAPICI OBUZ

PROFESÖR

İSTANBUL ÜNİVERSİTESİ İSTANBUL TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

Research topics OpenAlex
Academic summary YÖKSİS and OpenAlex counted separately.
Articles 146
YÖKSİS146 OpenAlex0
Projects 14
Books 16
Proceedings 79

Citation impact

OpenAlex YÖKSİS articles matched in OpenAlex: 110
h-index 35 Percentile in Türkiye: 100 #8 of 2,091 at their university by h-index
i10-index
65
Total citations
4,949
Top 0.4% in Türkiye
Per article
45.0
FWCI
3.20
1.00 = world average
World top 1%
8
World top 10%
33

Most cited articles

  1. Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study 2016 world top 1% 771 citations
  2. Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance 2009 world top 1% 264 citations
  3. Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study 2019 world top 1% 247 citations

h-index and citations are computed from the citation counts of this academic’s YÖKSİS articles matched in OpenAlex (not Google Scholar, WoS or Scopus). Unmatched articles are not included.

Field ranking

YÖKSİS ?

Index quartiles

?
Scopus (SJR) 123
  • Q1 66
  • Q2 38
  • Q3 11
  • Q4 8
WoS (JCR) 126
  • Q1 54
  • Q2 28
  • Q3 19
  • Q4 25
TR Index TR Index

8 articles

OpenAlex citation percentile
  • Top 1% 8
  • Top 10% 33
  • Avg 71.1%
  • n 116
Other counts

Scopus (SJR)

  • YÖKSİS rows 128

WoS (JCR)

  • YÖKSİS rows 131

TR Index

  • YÖKSİS rows 10 articles

Articles

Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.

Journals with publications

74 journals
Scopus (SJR)
Q1 66 Q2 38 Q3 11 Q4 8
WoS (JCR)
Q1 54 Q2 28 Q3 19 Q4 25
TR Index
8 articles

Article list

  1. 2025 QSM ‐Based Evidence of Brain Iron Accumulation in THAP1 Dystonia with Biallelic Mutation Movement Disorders Clinical Practice DOI 10.1002/mdc3.70432 YÖKSİS SJR Q2 JCR Q2 OpenAlex 36.9%
  2. 2025 Genome-wide association meta-analyses of drug-resistant epilepsy eBioMedicine DOI 10.1016/j.ebiom.2025.105675 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.5%
  3. 2025 Quantitative Iron Measurements in the Basal Ganglia of NBIA Patients Using QSM : Insights From a Tertiary Center Annals of Clinical and Translational Neurology DOI 10.1002/acn3.70161 YÖKSİS SJR Q1 JCR Q2 OpenAlex 76.5%
  4. 2025 Effects of immune modulatory treatment on language and psychiatric profile in patients with electrical status epilepticus in sleep (ESES) Epilepsy & Behavior DOI 10.1016/j.yebeh.2024.110225 YÖKSİS SJR Q2 JCR Q2 OpenAlex 78.1%
  5. 2025 Estrogen has a neuroprotective effect by preventing iron accumulation in Kufor Rakeb syndrome Biochemistry & Molecular Biology YÖKSİS SJR Q2 JCR Q3
  6. 2025 Missense variants in PKAN: insights from a multi-patient genetic analysis Neurogenetics DOI 10.1007/s10048-025-00864-1 YÖKSİS SJR Q3 JCR Q4 OpenAlex 29.7%
  7. 2025 A Comprehensive Overview of the Clinical, Electrophysiological, and Neuroimaging Features of BPAN: Insights From a New Case Series Annals of Clinical and Translational Neurology DOI 10.1002/acn3.70220 YÖKSİS SJR Q1 JCR Q2 OpenAlex 25.3%
  8. 2025 USP25 in genetic generalized epilepsy: a gene under scrutiny Brain DOI 10.1093/brain/awaf406 YÖKSİS SJR Q1 JCR Q1 OpenAlex 58.3%
  9. 2025 Factors Associated with COVID-19 Vaccination Status in Adolescents Diagnosed With Epilepsy Neuropsychiatric Investigation DOI 10.5152/NeuropsychiatricInvest.2025.24053 YÖKSİS OpenAlex 8.6%
  10. 2024 The Association Between Serum Levels of Glial Biomarkers, Clinical Severity and Electro-encephalography Features in Idiopathic West and Lennox-Gastaut Syndromes Archives of Neuropsychiatry DOI 10.29399/npa.28669 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 44.4%
  11. 2024 Exploring shared triggers and potential etiopathogenesis between migraine and idiopathic/genetic epilepsy: Insights from a multicenter tertiary-based study Clinical Neurology and Neurosurgery DOI 10.1016/j.clineuro.2024.108146 YÖKSİS SJR Q2 JCR Q3 OpenAlex 69.1%
  12. 2024 Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes Nature Neuroscience DOI 10.1038/s41593-024-01747-8 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.7%
  13. 2024 Epilepsy in dystrophinopathies: A retrospective cohort and review of the literature Epilepsy and Behavior DOI 10.1016/j.yebeh.2023.109595 YÖKSİS SJR Q2 JCR Q2 OpenAlex 56.2%
  14. 2024 Targeted resequencing reveals high-level mosaicism for a novel frameshift variant in WDR45 associated with beta-propeller protein-associated neurodegeneration International Journal of Neuroscience DOI 10.1080/00207454.2023.2208279 YÖKSİS SJR Q2 JCR Q4 OpenAlex 41.2%
  15. 2024 Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes nature neuroscience DOI 10.1016/j.seizure.2023.06.009 2 YÖKSİS records YÖKSİS SJR Q2 JCR Q2 OpenAlex 83.7%
  16. 2024 Lack of SPNS1 results in accumulation of lysolipids and lysosomal storage disease in mouse models JCI Insight DOI 10.1172/jci.insight.175462 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 94.6%
  17. 2023 Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity Springer Science and Business Media LLC DOI 10.1007/s13258-022-01344-8 2 YÖKSİS records YÖKSİS SJR Q3 JCR Q4 OpenAlex 62.7%
  18. 2023 Diagnosis of comorbid migraine without aura in patients with idiopathic/genetic epilepsy based on the gray zone approach to the International Classification of Headache Disorders 3 criteria Frontiers Media SA DOI 10.3389/fneur.2022.1103541 YÖKSİS SJR Q2 JCR Q2 OpenAlex 73.2%
  19. 2023 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Springer Science and Business Media LLC DOI 10.1038/s41588-023-01485-w YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.4%
  20. 2023 Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals Springer Science and Business Media LLC DOI 10.1038/s41467-023-39539-6 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.2%

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