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Akademisyen

GÜLAY CEYLANER

DOÇENT

LOKMAN HEKİM ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

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

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 25
  • Proje 0
  • Kitap 1
  • Bildiri 0
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 8 Q2 13 Q3 3 Q4 0
WoS (JCR) Q1 1 Q2 5 Q3 11 Q4 7
TR Index 2 makale

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

Üst %1 makale 0
Üst %10 makale 1
Ort. yüzdelik 67.6%
Üst %1 payı 0.0%
Üst %10 payı 4.0%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 25 yayın

Scopus (SJR)
Q1 8 Q2 13 Q3 3 Q4 0
WoS (JCR)
Q1 1 Q2 5 Q3 11 Q4 7
TR Index
2 makale

Makale listesi

  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 11.7%
  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 üst %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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