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Akademisyen

FİLİZ BAŞAK ERGİN

DOKTOR ÖĞRETİM ÜYESİ

GAZİ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

Araştırma konuları OpenAlex
Akademik özet YÖKSİS ve OpenAlex ayrı sayılır.
Makale 50
YÖKSİS50 OpenAlex0
Proje 2
Kitap 1
Bildiri 26

Atıf etkisi

OpenAlex YÖKSİS makalelerinden OpenAlex’te eşleşen: 4
h-indeks 4 Türkiye yüzdelik dilimi: 58 Üniversitesinde h-indekse göre 499. / 1.484
i10-indeks
4
Toplam atıf
151
Türkiye’de üst %26
Makale başına
37,8
FWCI
2,20
1,00 = dünya ortalaması
Dünyada üst %1
0
Dünyada üst %10
2

En çok atıf alan makaleleri

  1. Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss 2016 dünyada üst %10 61 atıf
  2. FOXF2 is required for cochlear development in humans and mice 2019 dünyada üst %10 42 atıf
  3. SLC26A4 mutations are associated with a specific inner ear malformation 2007 30 atıf

h-indeks ve atıflar, bu akademisyenin YÖKSİS makalelerinden OpenAlex’te eşleşenlerin atıf sayılarından hesaplanır (Google Scholar, WoS veya Scopus değildir). Eşleşmeyen makalelerin atıfı dahil değildir.

Alan sıralaması

YÖKSİS ?

Dizin çeyrekleri

?
Scopus (SJR) 47
  • Q1 20
  • Q2 21
  • Q3 3
  • Q4 3
WoS (JCR) 46
  • Q1 18
  • Q2 6
  • Q3 14
  • Q4 8
TR Index TR Index

2 makale

OpenAlex atıf yüzdelik
  • Üst %1 0
  • Üst %10 2
  • Ort. 80.4%
  • n 4
Diğer sayımlar

Scopus (SJR)

  • YÖKSİS satırı 47

WoS (JCR)

  • YÖKSİS satırı 46

Makaleler

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

Yayını olan dergiler

34 dergi
Scopus (SJR)
Q1 20 Q2 21 Q3 3 Q4 3
WoS (JCR)
Q1 18 Q2 6 Q3 14 Q4 8
TR Index
2 makale

Makale listesi

  1. 2025 Clinical, laboratory and molecular features of glycogen storage disease type 1a and 1b patients from Turkey: novel mutations and phenotypes European Journal of Pediatrics DOI 10.1007/s00431-025-06371-7 YÖKSİS SJR Q1 JCR Q1
  2. 2025 Expert opinion on clinical presentation, diagnosis and treatment of infantile onset pompe disease: a delphi study in Türkiye Turkish Journal of Medical Sciences DOI 10.55730/1300-0144.6005 YÖKSİS TR Index SJR Q3 JCR Q2
  3. 2024 Association between CLOCK gene polymorphisms with circadian rhythm, chrononutrition, dietary intake, and metabolic parameters in adolescents Frontiers in Public Health DOI 10.3389/fpubh.2024.1435460 YÖKSİS SJR Q1 JCR Q1
  4. 2024 A very rare presentation of mitochondrial elongation factor Tu deficiency-TUFM mutation and literature review Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2023-0569 YÖKSİS SJR Q2 JCR Q3
  5. 2023 A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation Elsevier BV DOI 10.1016/j.jbspin.2022.105490 YÖKSİS SJR Q2 JCR Q1
  6. 2022 Expected or unexpected clinical findings in liver glycogen storage disease type IX: distinct clinical and molecular variability Walter de Gruyter GmbH DOI 10.1515/jpem-2021-0278 YÖKSİS SJR Q2 JCR Q4
  7. 2022 m.3010G>A Değişikliğinin Türk Populasyonunda Siklik Kusma Sendromuna Etkisi Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi YÖKSİS TR Index
  8. 2022 MITOKONDRIYAL HASTALIK NEDENIYLE TETKIK EDILEN HASTALARDA M.16189T>C DEGIŞIKLIGININ METABOLIK SENDROM AÇISINDAN INCELENMESI Afyon Kocatepe Üniversitesi Kocatepe Tıp Dergisi YÖKSİS
  9. 2022 A Turkish case of incontinentia pigmenti with a deletion mutation at Inhibitor of kappa B kinase gamma gene Egyptian Journal of Medical Human Genetics DOI 10.1186/s43042-022-00215-x YÖKSİS SJR Q4 JCR Q4
  10. 2021 The first case with FBXL4 mutation successfully treated with a parenteral ketogenic diet for lactic acidosis Journal of Parenteral and Enteral Nutrition DOI 10.1002/jpen.2121 YÖKSİS SJR Q2 JCR Q3
  11. 2021 Hypophosphatasia: is it an underdiagnosed disease even by expert physicians? Journal of Bone and Mineral Metabolism DOI 10.1007/s00774-020-01193-z YÖKSİS SJR Q2 JCR Q3
  12. 2021 Congenital defects of glycosylation: Novel presentations with mainly neurological involvement and variable dysmorphic features American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.62247 YÖKSİS SJR Q2 JCR Q3
  13. 2021 Two patients from Turkey with a novel variant in the GM2A gene and review of the literature Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2020-0655 YÖKSİS SJR Q2 JCR Q4
  14. 2020 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida Genes DOI 10.3390/genes11040350 YÖKSİS SJR Q2 JCR Q2
  15. 2020 Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development JOURNAL OF CLINICAL INVESTIGATION DOI 10.1172/JCI136951 YÖKSİS SJR Q1 JCR Q1 OpenAlex 75.5%
  16. 2019 Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA DOI 10.1073/pnas.1810951116 YÖKSİS SJR Q1 JCR Q1
  17. 2019 FOXF2 is required for cochlear development in humans and mice HUMAN MOLECULAR GENETICS DOI 10.1093/hmg/ddy431 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 94.8%
  18. 2018 Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies MOLECULAR CYTOGENETICS DOI 10.1186/s13039-018-0390-4 YÖKSİS SJR Q2 JCR Q4
  19. 2018 Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability PLOS ONE DOI 10.1371/journal.pone.0208324 YÖKSİS SJR Q1 JCR Q2
  20. 2018 MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss HUMAN GENETICS DOI 10.1007/s00439-018-1901-4 YÖKSİS SJR Q1 JCR Q1

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