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akaturk Academic measurement
Academic summary YÖKSİS and OpenAlex counted separately.
Articles 35
YÖKSİS35 OpenAlex0
Projects 6
Books 0
Proceedings 77

Field ranking

YÖKSİS ?

Index quartiles

?
Scopus (SJR) 21
  • Q1 7
  • Q2 6
  • Q3 2
  • Q4 6
WoS (JCR) 25
  • Q1 3
  • Q2 3
  • Q3 7
  • Q4 12
TR Index TR Index

3 articles

OpenAlex citation percentile
  • Top 1% 0
  • Top 10% 0
  • Avg 44.0%
  • n 3
Other counts

Scopus (SJR)

  • YÖKSİS rows 21

WoS (JCR)

  • YÖKSİS rows 25

Proceedings

Conference proceedings recorded in YÖKSİS.

Records

Showing 20 / 77

  1. 2017 Anovel mutation in TCIRG1 gene in a Turkish patient with malignant autosomal recessive osteopetrosis ESHG 2017
  2. 2017 A novel mutation in TCIRG1 gene in a Turkish patient with malignant autosomal recessive osteopetrosis European Human Genetics Conference
  3. 2016 Identification of the germline mutations of p53 CHEK2 and PTEN geens in non BRCA1 2 mutation carrier high risk Trukish breast cancer patients European Human Genetics Conference
  4. 2017 Identification of a constitutional t(119)(q23p13) translocation inan Extranodal Natural Killer T cell Lmyphoma patient 11th EuropeanCytogenetics Conference
  5. 2017 Evaluation of three patients with Bannayan-Riley-Ruvalcaba Syndrome European Human Genetics Conference
  6. 2017 Evaluation of three patients with Bannayan-Riley Ruvalcaba syndrome ESHG 2017
  7. 2017 Conventional cytogenetics findings t(1221)(p13q22) translocationand 9p21deletion in pediatric ALL patients Conventional cytogenetics findings t(1221)(p13q22) translocationand 9p21deletion in pediatric ALL patients
  8. 2007 Combination of Hb Knossos Cod 27 G T and IVSII 745 C G in a Turkish Patient with Beta Thalassemia Major European Human Genetics Conference 2007
  9. 2010 Association of Several Genetic Variants with Myocardial Infarction A Pilot Study in Mediterranean Region 9. Ulusal Tıbbi Genetik Kongresi
  10. 2008 Meme ve Prostat Kanserli Hastalarda BRCA Genlerinin Kalıtsal Mutasyonlarının Önemi VIII.Ulusal Tıbbi Genetik Kongresi
  11. 2004 X Kromozom Etkinsizleştirilmesinin Meme Kanseri ile ilişkisi VI.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi
  12. 2005 BRCA1 BRCA2 VIII. Ulusal Meme Hastalıkları Kongresi
  13. 2005 Meme ve veya Over Kanserli Hastalarda BRCA1 ve BRCA2 Gen Mutasyonlarının Taranması VIII. Ulusal Meme Hastalıkları Kongresi
  14. 2004 JPediatric ALL li Olgularda t 12 21 Translokasyonun Önemi Türk Hematoloji Derneği XXXI.Ulusal Kongresi
  15. 2001 Antalya da Beta Talasemi ve Orak Hücre Anemisinin Moleküler Genetik Analiz Sonuçları III.Ulusal Pediatrik Hematoloji Kongresi
  16. 2004 Germline Mutations of BRCA1 ve BRCA2 Genes in High Risk Breast And Or Ovarian Cancer Turkish Patients Familial Cancer konferansı
  17. 2009 No Correlation Between RLIP76 Gene Polymorphisms and Drug Response in Epilepsy Mediterrranean Medical Genetics Meeting
  18. 2004 X Chromosome Inactivaiton and Breast Cancer European Human Genetics Conference 2004
  19. 2009 Periyodik Ateş Sendromlarında TNFRSF1A Gen Mutasyonlarının Rolü XVII. Ulusal Allerji ve Klinik İmmünoloji Kongresi
  20. 2000 Hematolojik Malignansilerde Sitogenetik Çalışmalar IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi

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