Fatma Tuba Eminoğlu

595 total citations
58 papers, 244 citations indexed

About

Fatma Tuba Eminoğlu is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Fatma Tuba Eminoğlu has authored 58 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Clinical Biochemistry, 19 papers in Molecular Biology and 14 papers in Physiology. Recurrent topics in Fatma Tuba Eminoğlu's work include Metabolism and Genetic Disorders (24 papers), Lysosomal Storage Disorders Research (12 papers) and Folate and B Vitamins Research (9 papers). Fatma Tuba Eminoğlu is often cited by papers focused on Metabolism and Genetic Disorders (24 papers), Lysosomal Storage Disorders Research (12 papers) and Folate and B Vitamins Research (9 papers). Fatma Tuba Eminoğlu collaborates with scholars based in Türkiye, United States and Italy. Fatma Tuba Eminoğlu's co-authors include Engi̇n Köse, Leyla Tümer, İlyas Okur, Alev Hasanoğlu, Serap Teber, Gürsel Biberoğlu, Fatih Süheyl Ezgü, Özlem Doğan, Yasemin Erten and Nilgün Karadağ and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Epilepsy Research.

In The Last Decade

Fatma Tuba Eminoğlu

47 papers receiving 241 citations

Peers

Fatma Tuba Eminoğlu

PHYSI

PPCH

RHEUM

İlyas Okur Türkiye

Tanyel Zübarioğlu Türkiye

Marian Girgis Egypt

Vladimı́r Bzdúch Slovakia

Hatice Serap Sivri Türkiye

Andrea M. Atherton United States

Natan Brand Israel

Paula Frassinetti Vasconcelos de Medeiros Brazil

Ebru Canda Türkiye

Lénaïg Abily-Donval France

İlyas Okur Türkiye

Fatma Tuba Eminoğlu

124 ×1.5

136 ×2.2

PHYSI

78 ×1.3

42 ×1.1

PPCH

86 ×2.5

RHEUM

Citations per year, relative to Fatma Tuba Eminoğlu Fatma Tuba Eminoğlu (= 1×) peers İlyas Okur

Countries citing papers authored by Fatma Tuba Eminoğlu

Since Specialization

Citations

This map shows the geographic impact of Fatma Tuba Eminoğlu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fatma Tuba Eminoğlu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fatma Tuba Eminoğlu more than expected).

Fields of papers citing papers by Fatma Tuba Eminoğlu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fatma Tuba Eminoğlu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fatma Tuba Eminoğlu. The network helps show where Fatma Tuba Eminoğlu may publish in the future.

Co-authorship network of co-authors of Fatma Tuba Eminoğlu

This figure shows the co-authorship network connecting the top 25 collaborators of Fatma Tuba Eminoğlu. A scholar is included among the top collaborators of Fatma Tuba Eminoğlu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Fatma Tuba Eminoğlu. Fatma Tuba Eminoğlu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Köse, Engi̇n, Figen Özçay, Halil İbrahim Aydın, et al.. (2025). Effect of empagliflozin treatment on laboratory and clinical findings of patients with glycogen storage disease type Ib: first study from Türkiye. Journal of Pediatric Endocrinology and Metabolism. 38(4). 391–398. 1 indexed citations

Kuloğlu, Zarife, Arzu Meltem Demir, Ceyda Tuna Kırşaçlıoğlu, et al.. (2025). Wolcott–Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure – a case report. Journal of Pediatric Endocrinology and Metabolism. 38(8). 868–872.

Yılmaz, Rezzak, et al.. (2025). Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor. Neurological Sciences. 46(9). 4361–4373.

Köse, Engi̇n, et al.. (2025). Challenges Faced by Newborns with Inherited Metabolic Disorders and Their Mothers During Antepartum, Intrapartum, and Postpartum Periods. Fetal and Pediatric Pathology. 44(1). 53–62.

Köse, Engi̇n, et al.. (2024). Türkiye’s First Multidisciplinary Gene Therapy Education Program: History and Plans for the Future. Journal of Contemporary Medicine. 14(2). 77–82.

Eminoğlu, Fatma Tuba, et al.. (2024). Diagnosis and Treatment of Newborns Referred to the Metabolism Department From the National Newborn Screening Program in Türkiye: A 5-Year Single-Center Experience. Turkish Journal of Pediatric Disease. 18(5). 274–280.

Köse, Engi̇n, et al.. (2024). Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review. Journal of Pediatric Endocrinology and Metabolism. 37(3). 260–270.

Köse, Engi̇n, Miraç Yıldırım, Suat Fítöz, et al.. (2024). Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis?. Pediatric Neurology. 155. 171–176.

Yıldırım, Miraç, et al.. (2024). Metabolic etiologies in children with infantile epileptic spasm syndrome: Experience at a tertiary pediatric neurology center. Brain and Development. 46(6). 213–218. 3 indexed citations

10.

Köse, Engi̇n, et al.. (2023). A different approach to the evaluation of the genotype-phenotype relationship in biotinidase deficiency: repeated measurement of biotinidase enzyme activity. Journal of Pediatric Endocrinology and Metabolism. 36(11). 1061–1071. 4 indexed citations

11.

Bakırarar, Batuhan, et al.. (2022). Pros and Cons of Telemedicine for Inherited Metabolic Disorders in a Developing Country During the COVID-19 Pandemic. Telemedicine Journal and e-Health. 28(11). 1604–1612. 5 indexed citations

12.

Eminoğlu, Fatma Tuba, et al.. (2022). Unmet Needs of Children with Inherited Metabolic Disorders in the COVID-19 Pandemic. Turkish Archives of Pediatrics. 57(3). 335–341. 5 indexed citations

13.

Eminoğlu, Fatma Tuba, Engi̇n Köse, Emel Okulu, et al.. (2021). Inherited metabolic disorders in the neonatal intensive care unit: Red flags to look out for. Pediatrics International. 64(1). e14953–e14953. 2 indexed citations

14.

Köse, Engi̇n, et al.. (2021). A case with Gaucher disease unable to reach enzyme replacement therapy because of COVID-19 quarantine: The first case from Turkey. Turkish Archives of Pediatrics. 56(3). 270–271. 2 indexed citations

15.

Köse, Engi̇n, et al.. (2021). An Atypical Presentation of Mevalonate Kinase Deficiency in Response to Colchicine Treatment. Molecular Syndromology. 13(2). 146–151. 1 indexed citations

16.

Köse, Engi̇n, et al.. (2021). A Mild Phenotype of Mitochondrial DNA Depletion Syndrome Type 13 with a Novel <b><i>FBXL4</i></b> Variant. Molecular Syndromology. 12(5). 294–299. 1 indexed citations

17.

Eminoğlu, Fatma Tuba, et al.. (2020). International classification of functioning, disability and health framework (ICF) based adaptive functioning outcomes of children with organic acidemias from a middle-income country. Brain and Development. 43(3). 389–395. 1 indexed citations

18.

Akduman, Hasan, Emel Okulu, Fatma Tuba Eminoğlu, et al.. (2019). Continuous venovenous hemodiafiltration in the treatment of newborns with an inborn metabolic disease: a single center experience. TURKISH JOURNAL OF MEDICAL SCIENCES. 50(1). 12–17. 5 indexed citations

19.

Doğan, Özlem, et al.. (2019). Effects of levetiracetam and valproic acid treatment on liver function tests, plasma free carnitine and lipid peroxidation in childhood epilepsies. Epilepsy Research. 153. 7–13. 23 indexed citations

20.

Eminoğlu, Fatma Tuba, et al.. (2018). An overlooked case of a treatable hyperinsulinemic hypoglycemia: congenital glycosylation defect type ıb. Türk Pediatri Arşivi. 55(1). 79–81. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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