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Academician

GÜLAY CEYLANER

Doçent

Lokman Hekim Üniversitesi Tıp Fakültesi Dahili Tıp Bilimleri Bölümü

Research topics OpenAlex
  1. Ana Dal Sağlık Bilimleri Temel Alanı
  2. Yan Dal Tıbbi Genetik
Articles 25 YÖKSİS 25 · OpenAlex 0 Total citations 401 h-index 12 · OpenAlex Q1 articles 8 Scopus · WoS Q1 1 Best field rank #12,569 / 39,749 Main field · top 31.6%

Citation impact

OpenAlex YÖKSİS articles matched in OpenAlex: 25 + YÖKSİS · co-author record: 6
h-index 12 Percentile in Türkiye: 89 #36 of 254 at their university by h-index
i10-index
15
Total citations
401
Top 16% in Türkiye
Per article
12.9
FWCI
0.93
1.00 = world average
World top 1%
0
World top 10%
1

Most cited articles

  1. Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin–Lowry syndrome 2006 51 citations
  2. A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data. 1995 37 citations
  3. Genetic abnormalities in Turkish women with premature ovarian failure 2010 34 citations
How is this computed?

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. 6 articles (32 citations) tagged with this academic’s YÖK author id in co-authors’ YÖKSİS records count only towards citations, h-index and i10; article counts, percentiles and rankings use their own YÖKSİS list.

Field ranking

YÖKSİS ?

Indexes and citation percentiles

?
TR Index 2 articles
OpenAlex citation percentile
Top 1%0
Top 10%1
Avg · n 25 %67.6
Other counts

Scopus (SJR)

  • YÖKSİS rows 24

WoS (JCR)

  • YÖKSİS rows 24

Articles

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

25articles

Journals with publications

18 journals

Narrow down

Scopus (SJR)
Q18 Q213 Q33 Q40
WoS (JCR)
Q11 Q25 Q311 Q47
TR Index
2articles

Article list

  1. 2021 The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS. Neuropediatrics DOI 10.1055/s-0040-1722691 YÖKSİS SJR Q2 JCR Q4 OpenAlex 62.1%
  2. 2021 Isolated congenital diaphragm hernia associated with homozygous SLIT3 gene variant in dizygous twins. European journal of medical genetics DOI 10.1016/j.ejmg.2021.104215 YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.0%
  3. 2016 A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus Elsevier BV DOI 10.1016/j.ejmg.2016.09.009 YÖKSİS SJR Q1 JCR Q3 OpenAlex 86.9%
  4. 2016 Genotypic and phenotypic features of the cystinosis patients from the south eastern part of turkey The Turkish Journal of Pediatrics DOI 10.24953/turkjped.2016.04.003 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 63.1%
  5. 2016 Congenital Glucose–Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene Springer Science and Business Media LLC DOI 10.1007/s10620-016-4348-2 YÖKSİS SJR Q1 JCR Q2 OpenAlex 73.0%
  6. 2013 Nephron-sparing Surgery for Renal Cell Carcinoma of the Allograft After Renal Transplantation: Report of Two Cases Elsevier BV DOI 10.1016/j.transproceed.2013.02.054 YÖKSİS SJR Q2 JCR Q3 OpenAlex 79.5%
  7. 2011 High frequency of p.Thr93Met in Smith‐Lemli‐Opitz syndrome patients in Turkey Wiley DOI 10.1111/j.1399-0004.2011.01750.x YÖKSİS SJR Q2 JCR Q2 OpenAlex 12.9%
  8. 2010 Genetic abnormalities in Turkish women with premature ovarian failure Wiley DOI 10.1016/j.ijgo.2010.03.023 YÖKSİS SJR Q2 JCR Q2 OpenAlex 86.0%
  9. 2009 Familial primary carpal tunnel syndrome with possible skipped generation Springer Science and Business Media LLC DOI 10.1007/s00431-009-1055-4 YÖKSİS SJR Q2 JCR Q2 OpenAlex 12.2%
  10. 2009 A boy with trisomy 13 presenting with a subtle clinical picture and metopic synostosis Wiley DOI 10.1002/ajmg.a.32912 YÖKSİS SJR Q2 JCR Q3 OpenAlex 82.1%
  11. 2009 Vascular endothelial growth factor +405 C/G polymorphism is highly associated with an increased risk of endometriosis in Turkish women Springer Science and Business Media LLC DOI 10.1007/s00404-009-1344-1 YÖKSİS SJR Q2 JCR Q4 OpenAlex top 10% OpenAlex 90.5%
  12. 2008 GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals Springer Science and Business Media LLC DOI 10.1007/s12041-008-0007-5 YÖKSİS SJR Q3 JCR Q4 OpenAlex 65.1%
  13. 2008 Autosomal dominant inheritance of congenital dislocation of the hip in 16 members of a family AVES YAYINCILIK A.Ş. DOI 10.3944/AOTT.2008.289 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 87.3%
  14. 2008 Neu-Laxova syndrome in an appropriate for gestational age newborn Scientific Scholar DOI 10.4103/0378-6323.44307 YÖKSİS SJR Q2 JCR Q4 OpenAlex 62.8%
  15. 2007 Chromosomal heteromorphisms may help for the diagnosis of uniparental disomy (UPD): a case report Wiley DOI 10.1002/pd.1814 YÖKSİS SJR Q1 JCR Q3 OpenAlex 62.2%
  16. 2007 Prenatal diagnosis of a Turkish Bartsocas–Papas syndrome case with upper limb pterigia Wiley DOI 10.1002/pd.1723 YÖKSİS SJR Q1 JCR Q3 OpenAlex 14.0%
  17. 2007 Evaluation of 2407 fetuses in a Turkish population Wiley DOI 10.1002/pd.1762 YÖKSİS SJR Q1 JCR Q3 OpenAlex 81.3%
  18. 2006 Extremely skewed X‐chromosome inactivation patterns in women with recurrent spontaneous abortion Wiley DOI 10.1111/j.1479-828X.2006.00622.x YÖKSİS SJR Q2 JCR Q4 OpenAlex 84.1%
  19. 2006 Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin–Lowry syndrome Wiley DOI 10.1111/j.1399-0004.2006.00660.x YÖKSİS SJR Q2 JCR Q2 OpenAlex 83.8%
  20. 2006 Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population Wiley DOI 10.1002/pd.1378 YÖKSİS SJR Q1 JCR Q3 OpenAlex 78.1%

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