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.
Makale listesi
- 2025 Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum YÖKSİS TR Index SJR Q2 JCR Q1 OpenAlex 28.9%
- 2025 Two Siblings with Missense Homozygous ABCA3 R43H Mutation Showing Good Response to Glucocorticoid YÖKSİS SJR Q2 JCR Q2 OpenAlex 8.7%
- 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 YÖKSİS SJR Q1 JCR Q1 OpenAlex 11.8%
- 2024 A Case of Primary Ciliary Dyskinesia Syndrome with Situs Ambiguous YÖKSİS TR Index SJR Q4 OpenAlex 2.8%
- 2023 An intermediate phenotype in IDH related enchondromatosis spectrum YÖKSİS SJR Q2 JCR Q4 OpenAlex 44.8%
- 2022 A New Variant of the IER3IP1 Gene: The First Case of Microcephaly, Epilepsy, and Diabetes Syndrome 1 from Turkey YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex 58.9%
- 2022 EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 93.2%
- 2022 Clinical and molecular genetic findings of Crisponi/cold-induced sweating syndrome (CS/CISS) spectrum in patients from Turkey YÖKSİS SJR Q1 JCR Q2 OpenAlex 48.5%
- 2022 The evaluation of potential global impact of the N501Y mutation in SARS-COV-2 positive patients YÖKSİS SJR Q1 JCR Q1 OpenAlex 81.3%
- 2022 Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases YÖKSİS SJR Q2 JCR Q2 OpenAlex 82.9%
- 2022 How to Manage Low Estriol Levels in Pregnancies, One Center Experience YÖKSİS TR Index SJR Q4 JCR Q2 OpenAlex 87.4%
- 2022 The Effect of Maternal Age on the Incidence of Major Malformations and Operations in Children with Down Syndrome YÖKSİS TR Index SJR Q4 JCR Q2 OpenAlex 61.8%
- 2022 Effects of Chromosomal Translocations on Sperm Count in Azoospermic and Oligospermic Cases YÖKSİS TR Index JCR Q4 OpenAlex 58.4%
- 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. YÖKSİS TR Index SJR Q4 JCR Q2 OpenAlex 71.9%
- 2022 Comparative Analysis of Spermiogram, Hormonal Profile and Genetic Analysis Results in Patients Applying with Male Infertility: A Single Center Experience. YÖKSİS TR Index OpenAlex 59.4%
- 2021 The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered YÖKSİS SJR Q1 JCR Q1 OpenAlex 59.8%
- 2021 SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 96.7%
- 2021 High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.0%
- 2021 Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.3%
- 2021 Effect of different storage conditions on COVID‐19 RT‐PCR results YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 91.0%