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akaturk Akademik ölçüm

Akademisyen

ELİF YILMAZ GÜLEÇ

DOÇENT

İSTANBUL MEDENİYET ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 64
  • Proje 0
  • Kitap 6
  • Bildiri 64
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 25 Q2 23 Q3 2 Q4 5
WoS (JCR) Q1 25 Q2 11 Q3 11 Q4 10
TR Index 16 makale

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

Üst %1 makale 4
Üst %10 makale 20
Ort. yüzdelik 65.8%
Üst %1 payı 6.6%
Üst %10 payı 32.8%

Makaleler

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

Dizin filtreleri

Toplam 64 yayın

Makale listesi

  1. 2025 Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum Balkan Medical Journal DOI 10.4274/balkanmedj.galenos.2025.2025-9-81 YÖKSİS TR Index SJR Q2 JCR Q1 OpenAlex 28.9%
  2. 2025 Two Siblings with Missense Homozygous ABCA3 R43H Mutation Showing Good Response to Glucocorticoid Indian Journal of Pediatrics DOI 10.1007/s12098-025-05602-x YÖKSİS SJR Q2 JCR Q2 OpenAlex 8.7%
  3. 2025 C-terminal TREX1 c.914A>G variant in a patient with IgA nephropathy and thrombotic microangiopathy: expanding the clinical and genetic spectrum of IgA nephropathy with microangiopathic lesions Clinical Kidney Journal DOI 10.1093/ckj/sfaf191 YÖKSİS SJR Q1 JCR Q1 OpenAlex 11.8%
  4. 2024 A Case of Primary Ciliary Dyskinesia Syndrome with Situs Ambiguous Respir Case Rep DOI 10.5505/respircase.2024.89106 YÖKSİS TR Index SJR Q4 OpenAlex 2.8%
  5. 2023 An intermediate phenotype in IDH related enchondromatosis spectrum EUROPEAN JOURNAL OF MEDICAL GENETICS Elsevier BV DOI 10.1016/j.ejmg.2023.104697 YÖKSİS SJR Q2 JCR Q4 OpenAlex 44.8%
  6. 2022 A New Variant of the IER3IP1 Gene: The First Case of Microcephaly, Epilepsy, and Diabetes Syndrome 1 from Turkey JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY Galenos Yayinevi DOI 10.4274/jcrpe.galenos.2022.2022-8-12 YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex 58.9%
  7. 2022 EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis AMERICAN JOURNAL OF HUMAN GENETICS Elsevier BV DOI 10.1016/j.ajhg.2022.10.010 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 93.2%
  8. 2022 Clinical and molecular genetic findings of Crisponi/cold-induced sweating syndrome (CS/CISS) spectrum in patients from Turkey Clinical Genetics DOI 10.1111/cge.14177 YÖKSİS SJR Q1 JCR Q2 OpenAlex 48.5%
  9. 2022 The evaluation of potential global impact of the N501Y mutation in SARS-COV-2 positive patients journal of medical virology DOI 10.1002/jmv.27413 YÖKSİS SJR Q1 JCR Q1 OpenAlex 81.3%
  10. 2022 Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases Frontiers in Genetics DOI 10.3389/fgene.2022.861236 YÖKSİS SJR Q2 JCR Q2 OpenAlex 82.9%
  11. 2022 How to Manage Low Estriol Levels in Pregnancies, One Center Experience Medeniyet Medical Journal DOI 10.4274/MMJ.galenos.2022.22747 YÖKSİS TR Index SJR Q4 JCR Q2 OpenAlex 87.4%
  12. 2022 The Effect of Maternal Age on the Incidence of Major Malformations and Operations in Children with Down Syndrome Medeniyet Medical Journal DOI 10.4274/MMJ.galenos.2022.09086 YÖKSİS TR Index SJR Q4 JCR Q2 OpenAlex 61.8%
  13. 2022 Effects of Chromosomal Translocations on Sperm Count in Azoospermic and Oligospermic Cases Journal of Basic and Clinical Health Sciences DOI 10.30621/jbachs.1069678 YÖKSİS TR Index JCR Q4 OpenAlex 58.4%
  14. 2022 Diagnostic Value of Microarray Method in Autism Spectrum Disorder, Intellectual Disability, and Multiple Congenital Anomalies and Some Candidate Genes for Autism: Experience of Two Centers. Medeniyet Medical Journal DOI 10.4274/mmj.galenos.2022.70962 YÖKSİS TR Index SJR Q4 JCR Q2 OpenAlex 71.9%
  15. 2022 Comparative Analysis of Spermiogram, Hormonal Profile and Genetic Analysis Results in Patients Applying with Male Infertility: A Single Center Experience. Sağlık Bilimlerinde Değer DOI 10.33631/sabd.1054912 YÖKSİS TR Index OpenAlex 59.4%
  16. 2021 The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered European Journal of Human Genetics DOI 10.1038/s41431-020-00743-3 YÖKSİS SJR Q1 JCR Q1 OpenAlex 59.8%
  17. 2021 SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype The American Journal of Human Genetics DOI 10.1016/j.ajhg.2021.09.007 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 96.7%
  18. 2021 High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population The American Journal of Human Genetics DOI 10.1016/j.ajhg.2021.08.009 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.0%
  19. 2021 Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome The American Journal of Human Genetics DOI 10.1016/j.ajhg.2021.04.016 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.3%
  20. 2021 Effect of different storage conditions on COVID‐19 RT‐PCR results Journal of medical virology DOI 10.1002/jmv.27204 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 91.0%

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