İçeriğe geç
akaturk Akademik ölçüm
Giriş Kayıt

Akademisyen

ASLI GÜNDOĞDU EKEN

ARAŞTIRMA GÖREVLİSİ

BOĞAZİÇİ ÜNİVERSİTESİ FEN FAKÜLTESİ MOLEKÜLER BİYOLOJİ VE GENETİK BÖLÜMÜ

  • Ana Dal Fen Bilimleri ve Matematik Temel Alanı
  • Yan Dal Biyoloji

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 26
  • Proje 0
  • Kitap 0
  • Bildiri 0
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 12 Q2 7 Q3 3 Q4 1
WoS (JCR) Q1 6 Q2 11 Q3 5 Q4 3
TR Index 1 makale

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

Üst %1 makale 2
Üst %10 makale 5
Ort. yüzdelik 73.1%
Üst %1 payı 9.1%
Üst %10 payı 22.7%

Makaleler

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

Dizin filtreleri

Toplam 26 yayın

Scopus (SJR)
Q1 12 Q2 7 Q3 3 Q4 1
WoS (JCR)
Q1 6 Q2 11 Q3 5 Q4 3
TR Index
1 makale

Makale listesi

  1. 2018 Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey Archives of Neuropsychiatry DOI 10.5152/npa.2017.20525 YÖKSİS SJR Q4 JCR Q4 OpenAlex 10.1%
  2. 2018 Clinical and molecular characterization and response to acitretin in three families with Sjögren-Larsson syndrome International Journal of Dermatology DOI 10.1111/ijd.14013 YÖKSİS SJR Q2 JCR Q3 OpenAlex 65.9%
  3. 2018 Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2 Neurodegenerative Diseases DOI 10.1159/000486201 YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 90.1%
  4. 2017 Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE) European Journal of Paediatric Neurology DOI 10.1016/j.ejpn.2017.05.001 YÖKSİS SJR Q1 JCR Q2 OpenAlex 51.7%
  5. 2016 Atypical Features in a Large Turkish Family Affected with Friedreich Ataxia Neurological Medicine DOI 10.1155/2016/4515938 YÖKSİS JCR Q4 OpenAlex 62.3%
  6. 2016 SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations Seizure DOI 10.1016/j.seizure.2016.05.008 YÖKSİS SJR Q1 JCR Q2 OpenAlex 73.6%
  7. 2014 FBXO7eR498X mutation: Phenotypic variability from chorea to early onset parkinsonism within a family Parkinsonism and Related Disorders DOI 10.1016/j.parkreldis.2014.07.016 YÖKSİS SJR Q3 JCR Q3 OpenAlex 86.3%
  8. 2009 Two Young Sisters with Spinocerebellar Ataxia Type 2 Showing Different Clinical Progression of Disease CEREBELLUM DOI 10.1007/s12311-008-0080-6 YÖKSİS SJR Q1 JCR Q2 OpenAlex 40.5%
  9. 2009 Bell's palsy and choreiform movements during peginterferon alpha and ribavirin therapy WORLD JOURNAL OF GASTROENTEROLOGY DOI 10.3748/wjg.15.3694 YÖKSİS SJR Q1 JCR Q3 OpenAlex 58.5%
  10. 2023 Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals Nature Communications DOI 10.1038/s41467-023-39539-6 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.2%
  11. 2021 Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations Epilepsia DOI 10.1111/epi.16922 YÖKSİS SJR Q1 JCR Q1 OpenAlex 82.4%
  12. 2021 Distinct gene-set burden patterns underlie common generalized and focal epilepsies EBio Midicine DOI 10.1016/j.ebiom.2021.103588 YÖKSİS SJR Q1 JCR Q1 OpenAlex 85.4%
  13. 2020 Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects BRAIN DOI 10.1093/brain/awaa171 YÖKSİS SJR Q3 JCR Q3 OpenAlex üst %10 OpenAlex 98.3%
  14. 2019 Possible role of SCN4A skeletal muscle mutation in apnea during seizure Epilepsia Open DOI 10.1002/epi4.12347 YÖKSİS SJR Q2 JCR Q2 OpenAlex 58.9%
  15. 2019 Polygenic burden in focal and generalized epilepsies Brain DOI 10.1093/brain/awz292 YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 98.8%
  16. 2019 Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals American Journal of Human Genetics DOI 10.1016/j.ajhg.2019.05.020 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.8%
  17. 2018 ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree European Journal of Human Genetics DOI 10.1038/s41431-018-0107-5 YÖKSİS SJR Q1 JCR Q2 OpenAlex 85.8%
  18. 2018 Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families Neurology Genetics DOI 10.1212/NXG.0000000000000218 YÖKSİS SJR Q1 JCR Q2 OpenAlex 79.2%
  19. 2016 Successful treatment of Juvenile parkinsonism with bilateral subthalamic deep brain stimulation in a 14-year-old patient with parkin gene mutation Parkinsonism and Related Disorder DOI 10.1016/j.parkreldis.2016.01.018 YÖKSİS SJR Q1 JCR Q1 OpenAlex 82.9%
  20. 2015 The distinct genetic pattern of ALS in Turkey and novel mutations Neurobiol Aging YÖKSİS SJR Q1 JCR Q1

Akademisyenlere dön