Academician
ÇİĞDEM SEHER KASAPKARA
PROFESÖR
GAZİ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk Metabolizma Hastalıkları (Çocuk Sağlığı ve Hastalıkları)
A quick look at recorded outputs — details below.
- Articles 116
- Projects 0
- Books 28
- Proceedings 126
- Patents 0
- Artistic 0
Scopus (SJR)
Q1
18
Q2
35
Q3
32
Q4
6
WoS (JCR)
Q1
9
Q2
15
Q3
24
Q4
45
TR Index
19
articles
Field+year+type normalized OpenAlex percentiles — not Clarivate ESI / SciVal.
Top 1% articles
1
Top 10% articles
2
Avg percentile
61.3%
Top 1% share
7.7%
Top 10% share
15.4%
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Article list
- 2025 Expert opinion on clinical presentation, diagnosis and treatment of infantile onset pompe disease: a delphi study in Türkiye YÖKSİS TR Index SJR Q3 JCR Q2
- 2025 Long‐Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response YÖKSİS SJR Q1 JCR Q2
- 2025 Genetic, neuroimaging, and clinical characteristics of a cohort of individuals with L-2-hydroxyglutaric aciduria from Türkiye YÖKSİS SJR Q3 JCR Q3
- 2025 Evaluation of Lysosphingolipid Analysis for the Diagnosis of Lysosomal Storage Disease YÖKSİS SJR Q3 JCR Q4
- 2025 Psychiatric Presentation of Hereditary Coproporphyria with Coproporphyrinogen Oxidase Gene Mutation c.734 C>T: A Case Report YÖKSİS TR Index SJR Q3 JCR Q4
- 2025 Effect of empagliflozin treatment on laboratory and clinical findings of patients with glycogen storage disease type Ib: first study from Türkiye YÖKSİS SJR Q3 JCR Q3
- 2025 Outcome of Haemopoietic Stem Cell Transplantation in 21 Patients With Alpha‐Mannosidosis YÖKSİS SJR Q1 JCR Q2 OpenAlex 88.6%
- 2025 The First Case of 4H Syndrome with Type 1 Diabetes Mellitus YÖKSİS TR Index SJR Q2 JCR Q2
- 2025 D-bifunctional protein deficiency type III: Two Turkish cases and a novel HSD17B4 gene variant YÖKSİS SJR Q3 JCR Q4
- 2025 Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect YÖKSİS SJR Q3 JCR Q4
- 2025 Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy YÖKSİS SJR Q3 JCR Q4
- 2025 Evaluation of the Effect of Diet Adherence on Nutritional Status and Metabolic Control in Children with Phenylketonuria Consuming a Phenylalanine-Restricted Diet: A Single-Center Study YÖKSİS TR Index
- 2024 Sepiapterin Reductase Deficiency Misdiagnosed as Neurological Sequelae of Meningitis YÖKSİS SJR Q3 JCR Q4 OpenAlex 56.3%
- 2024 Long-term clinical evaluation of patients with alpha-mannosidosis – A multicenter study YÖKSİS SJR Q2 JCR Q3
- 2024 Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency YÖKSİS SJR Q1 JCR Q1 OpenAlex 80.5%
- 2024 Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration YÖKSİS SJR Q2 JCR Q3 OpenAlex 1.3%
- 2024 Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals YÖKSİS SJR Q2 JCR Q2
- 2024 Mitochondrial DNA Depletion Syndromes Gene Panel versus Clinical Exome Sequencing in Children with Suspected Mitochondrial Hepatopathies YÖKSİS SJR Q3 JCR Q4
- 2024 Is 5-Oxoprolinase Deficiency More than Just a Benign Condition? YÖKSİS SJR Q3 JCR Q4
- 2024 Mitochondrial phosphate‐carrier deficiency mimicking infantile‐onset Pompe disease YÖKSİS SJR Q2 JCR Q3