Academician profile · PROFESÖR
ASLI SUBAŞIOĞLU
İZMİR KATİP ÇELEBİ ÜNİVERSİTESİ
- TIP FAKÜLTESİ
- DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Scopus (SJR)
Q1
8
Q2
15
Q3
9
Q4
8
WoS (JCR)
Q1
7
Q2
7
Q3
8
Q4
18
TR Index
9
articles
Articles
- 2022 Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
- 2026 Clinical Significance of MTHFR C677T and A1298C Polymorphisms in Adult Patients with ALL and NHL
- 2026 Clinicopathological and genotypic characteristics of colorectal cancer patients carrying a germline MUTYH mutation
- 2026 Expanding the Genetic and Phenotypic Spectrum of DYT‐VPS16: The Importance of Splice‐Site Variants
- 2026 A rare large homozygous deletion of the HFE gene in a patient with hemochromatosis: a case report
- 2025 Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a Family
- 2025 Lynch syndrome association and clinicopathological features in early-onset colorectal cancers: A single-center retrospective study
- 2024 IL-1 blocking experience in a case with Majeed syndrome diagnosed in adulthood
- 2024 Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss
- 2023 Genetic, Surgical and Oncological Approach to Breast Cancer, with BRCA1, BRCA2, CDH1, PALB2, PTEN and TP53 Variants
- 2023 De Novo BETA-2 adrenergic receptor gene variant associated with obesity
- 2023 Afetlerde Kimliklendirme ve Genetik Yaklaşımlar
- 2023 A Rare Neuromuscular Disease: Limb Girdle Muscular DystrophyR18 Case Report
- 2022 Somut Olmayan Kültürel Miras Unsurlarından Ebru Sanatının Ortaokul Öğrencilerindeki Farkındalık Durumunda Medyanın Etkisi
- 2022 TEKRARLAYAN GEBELİK KAYBI OLAN HASTALARIN TROMBOFİLİ PANELİNİN RETROSPEKTİF ANALİZİ
- 2021 Mitochondrial Mutations in Multiple Sclerosis Patients with Atypical Optic Neuropathy
- 2021 Kronik Lenfositik Lösemi/Lenfoma Hastalarımızın Tek Merkezli 5 Yıllık Retrospektif Değerlendirmesi
- 2020 Factors influencing the acceptance ofprenatal testing by pregnant women
- 2020 Radixin modulates the function of outer hair cell stereocilia
- 2020 A case with a rare chromosomal abnormality: isochromosome 18p