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

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

#	Title	Journal	Authors	Indexed citations
1	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	Engi̇n Köse, Figen Özçay et al.	1
2	Wolcott–Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure – a case report	Journal of Pediatric Endocrinology and Metabolism	Zarife Kuloğlu, Arzu Meltem Demir et al.	0
3	Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor	Neurological Sciences	Rezzak Yılmaz, Ahmet Yalçın et al.	0
4	Challenges Faced by Newborns with Inherited Metabolic Disorders and Their Mothers During Antepartum, Intrapartum, and Postpartum Periods	Fetal and Pediatric Pathology	Engi̇n Köse, Fatma Tuba Eminoğlu et al.	0
5	Türkiye’s First Multidisciplinary Gene Therapy Education Program: History and Plans for the Future	Journal of Contemporary Medicine	Engi̇n Köse, Ömer Erdeve et al.	0
6	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	Fatma Tuba Eminoğlu et al.	0
7	Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review	Journal of Pediatric Endocrinology and Metabolism	Engi̇n Köse, Fatma Tuba Eminoğlu et al.	0
8	Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis?	Pediatric Neurology	Engi̇n Köse, Miraç Yıldırım et al.	0
9	Metabolic etiologies in children with infantile epileptic spasm syndrome: Experience at a tertiary pediatric neurology center	Brain and Development	Miraç Yıldırım, Engi̇n Köse et al.	3
10	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	Engi̇n Köse, Fatma Tuba Eminoğlu et al.	4
11	Pros and Cons of Telemedicine for Inherited Metabolic Disorders in a Developing Country During the COVID-19 Pandemic	Telemedicine Journal and e-Health	Batuhan Bakırarar, Engi̇n Köse et al.	5
12	Unmet Needs of Children with Inherited Metabolic Disorders in the COVID-19 Pandemic	Turkish Archives of Pediatrics	Fatma Tuba Eminoğlu et al.	5
13	Inherited metabolic disorders in the neonatal intensive care unit: Red flags to look out for	Pediatrics International	Fatma Tuba Eminoğlu, Engi̇n Köse et al.	2
14	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	Engi̇n Köse, Fatma Tuba Eminoğlu et al.	2
15	An Atypical Presentation of Mevalonate Kinase Deficiency in Response to Colchicine Treatment	Molecular Syndromology	Engi̇n Köse, Serdar Ceylaner et al.	1
16	A Mild Phenotype of Mitochondrial DNA Depletion Syndrome Type 13 with a Novel <b><i>FBXL4</i></b> Variant	Molecular Syndromology	Engi̇n Köse, Fatma Tuba Eminoğlu et al.	1
17	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	Fatma Tuba Eminoğlu et al.	1
18	Continuous venovenous hemodiafiltration in the treatment of newborns with an inborn metabolic disease: a single center experience	TURKISH JOURNAL OF MEDICAL SCIENCES	Hasan Akduman, Emel Okulu et al.	5
19	Effects of levetiracetam and valproic acid treatment on liver function tests, plasma free carnitine and lipid peroxidation in childhood epilepsies	Epilepsy Research	Özlem Doğan, Serap Teber et al.	23
20	An overlooked case of a treatable hyperinsulinemic hypoglycemia: congenital glycosylation defect type ıb	Türk Pediatri Arşivi	Fatma Tuba Eminoğlu et al.	1

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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