Skip to content
akaturk Academic measurement
  1. Ana Dal Sağlık Bilimleri Temel Alanı
  2. Yan Dal Nöroloji
Academic summary YÖKSİS and OpenAlex counted separately.
Articles 95
YÖKSİS95 OpenAlex0
Projects 11
Books 17
Proceedings 77

Citation impact

OpenAlex YÖKSİS articles matched in OpenAlex: 71
h-index 20 Percentile in Türkiye: 98 #160 of 2,315 at their university by h-index
i10-index
33
Total citations
4,035
Top 0.5% in Türkiye
Per article
56.8
FWCI
2.51
1.00 = world average
World top 1%
4
World top 10%
14

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) 78
  • Q1 29 %37.2
  • Q2 24 %30.8
  • Q3 16 %20.5
  • Q4 9 %11.5
WoS (JCR) 78
  • Q1 15 %19.0
  • Q2 20 %25.3
  • Q3 25 %31.6
  • Q4 19 %24.1
TR Index 10 articles
OpenAlex citation percentile
Top 1%4
Top 10%14
Avg · n 74 %63.0
Other counts

Scopus (SJR)

  • YÖKSİS rows 81

WoS (JCR)

  • Best Q 78 Q1 15 Q2 20 Q3 25 Q4 18
  • YÖKSİS rows 81

TR Index

  • YÖKSİS rows 11 articles

Proceedings

Conference proceedings recorded in YÖKSİS.

77proceedings

Records

Showing 20 / 77

  1. 2018 The expression of epidermal growth factor (EGF) and keratinocyte growth factor (KGF) in skin biopsy of amyotrophic lateral sclerosis patients AAN Congress 2018
  2. 2018 The expression of epidermal growth factor (EGF) and keratinocyte growth factor (KGF) in skin biopsy of amyotrophic lateral sclerosis patients AAN Congress 2018
  3. 2017 The Evaluation of Small Fibers in Multiple Sclerosis American Academy of Neurology
  4. 2019 Toscana virus associated with Guillain-Barré Syndrome: A case-control study 2019 PNS Meeting
  5. 2019 Erişkin Kas Hastalarında Fiziksel Aktiviteyi Objektif ve Subjektif Olarak Değerlendiren Yöntemlerin Karşılaştırılması TND II. Nöromusküler Hastalıklar Kongresi
  6. 2018 The functional and structural evaluation of small fibers in asymptomatic patients with Val30Met mutation 15th ICNMD Congress
  7. 2017 İmmünsupresif Kullanan Myastenia Gravis Hastalarının Yan Etki Profillerinin Değerlendirilmesi TND NÖROMUSKÜLER HASTALIKLAR KONGRESİ
  8. 2015 A Novel Mutation in the HTRA1 Gene in a Turkish Family with CARASIL European Academy of Neurology Meeting 2015 18 June Berlin European Academy of Neurology Meeting;
  9. — Precision diagnosis of myopathies through clinical exome sequencing 30th world muscle society congress
  10. 2020 MİYASTENİA GRAVİS HASTALARINDA RİTUKSİMAB TEDAVİSİ İLE KAS SPESİFİK KİNAZ (MUSK) ANTİKORLARINDANEGATİFLEŞME VE KLİNİK REMİSYON 56. ULUSAL NÖROLOJİ KONGRESİ
  11. 2019 Evaluation of the role of anti-sulfatide and anti-myelin oligodendrocyte glycoprotein (MOG) antibodies in demyelinating leukodystrophies. SSIEM 2019
  12. 2019 A novel ARMS-PCR assay for screening MT-TL1 mutations causing mitochondrial cytopathies 44th FEBS Congress
  13. 2019 Laboratory diagnosis of Metachromatic Leukodystrophy requires more than arylsulfatase A assay 44th FEBS Congress
  14. 2019 Nöroloji Yoğun Bakım Ünitesi'ndeki İnme Hastalarında Yoğun Bakım Ünitesinde Edinilmiş Güçsüzlüğün (YBÜ-EG) Multimodal İncelemesi 35. ULUSAL KLİNİK NÖROFİZYOLOJİ EEG-EMG KONGRESİ
  15. 2019 Multimodal Assessment Of Intensive Care Unit-Acquired Weakness (ICU-AW) In Severe Acute Stroke Patients 2019 PNS Meeting
  16. 2018 DONDURULMUŞ OLARAK BANKALANAN KAS BİYOPSİSİ ÖRNEKLERİNDEN PRİMER MİYOBLAST HÜCRE KÜLTÜRÜ KURULMASI 54. Ulusal Nöroloji Kongresi
  17. 2018 Metakromatik lökodistrofi hastalığının doğru ve erken tanısında önemli laboratuvar testleri 6. Uluslarası katılımlı lizozomal hastalıklar kongresi
  18. 2022 Home-infusion experience in patients with Pompe disease receiving avalglucosidase alfa during three clinical trials (COMET, NEO-EXT, and Mini-COMET) 18th Annual WORLDSymposium
  19. 2015 G Inal Gültekin 1 B Toptas Hekimog lu 1 Z Görmez 2 H Durmus 3 H Demirci 2 M Sag ırog lu 2 Y Parman 3 F Deymeer 3 H Yılmaz 1 S Pençe 1 C Kurt 4 E Tan 4 S Özdamar 4 U Giger 5 O Öztürk 1 P Serdarog lu Oflazer 3 Myophosphorylase PYGM mutations in Turkish patients with McArdle disease A next generation sequencing study October 2015 Neuromuscular Disorders Volume 25 Supplement 2 S145 S334 20th International Congress of The World Muscle Society
  20. 2023 Evaluation of the role of glial factors in the pathogenesis of spinal muscular atrophy 2023 Neuromuscular Study Group Annual Scientific Meeting

← Back to academicians