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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

Articles

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

95articles

Journals with publications

55 journals

Narrow down

Scopus (SJR)
WoS (JCR)
TR Index

Article filter applied. Journal filter: Neuromuscular Disorders Clear filter ×

Article list

4 / 95 articles

  1. 2022 The functional and structural evaluation of small fibers in asymptomatic carriers of p. Val50Met mutation NEUROMUSCULAR DISORDERS YÖKSİS SJR Q1 JCR Q3
  2. 2018 A database for screening and registering late onset Pompe disease in Turkey Neuromuscular Disorders DOI doi.org/10.1016/j.nmd.2017.12.008 YÖKSİS SJR Q1 JCR Q3
  3. 2017 Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease Neuromuscular Disorders DOI 10.1016/j.nmd.2017.06.004 YÖKSİS SJR Q1 JCR Q3 OpenAlex 84.3%
  4. 2015 Three Turkish families with different transthyretin mutations Neuromuscular Disorders DOI 10.1016/j.nmd.2015.05.010 YÖKSİS SJR Q1 JCR Q2 OpenAlex 66.7%

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