Elif Özsu

489 total citations
52 papers, 318 citations indexed

About

Elif Özsu is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Elif Özsu has authored 52 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 16 papers in Endocrinology, Diabetes and Metabolism and 12 papers in Genetics. Recurrent topics in Elif Özsu's work include Pancreatic function and diabetes (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Thyroid Disorders and Treatments (4 papers). Elif Özsu is often cited by papers focused on Pancreatic function and diabetes (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Thyroid Disorders and Treatments (4 papers). Elif Özsu collaborates with scholars based in Türkiye, United States and United Kingdom. Elif Özsu's co-authors include Gül Yeşiltepe Mutlu, Şükrü Hatun, Filiz Çizmecioğlu, Ferah Genel, Zeynep Şıklar, Gürkan Altun, Serdar Ceylaner, Kadir Babaoğlu, Allison Bahm and Merih Berberoğlu and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Clinical Endocrinology.

In The Last Decade

Elif Özsu

41 papers receiving 312 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Elif Özsu Türkiye 9 73 61 59 54 48 52 318
Pramila Kalra India 12 59 0.8× 78 1.3× 85 1.4× 129 2.4× 31 0.6× 67 441
Moon Bae Ahn South Korea 11 40 0.5× 96 1.6× 33 0.6× 123 2.3× 61 1.3× 58 410
Paola Galoppi Italy 11 43 0.6× 65 1.1× 62 1.1× 85 1.6× 92 1.9× 42 349
Anastasios Serbis Greece 11 91 1.2× 64 1.0× 31 0.5× 127 2.4× 42 0.9× 42 363
Philippos Kaldrymides Greece 8 45 0.6× 68 1.1× 122 2.1× 112 2.1× 36 0.8× 12 383
Vardit Gepstein Israel 8 36 0.5× 38 0.6× 154 2.6× 55 1.0× 58 1.2× 17 312
Serena Ottanelli Italy 11 55 0.8× 36 0.6× 26 0.4× 77 1.4× 43 0.9× 26 413
О. D. Belyaeva Russia 10 91 1.2× 35 0.6× 140 2.4× 25 0.5× 28 0.6× 45 318
Silvana Lauriola Italy 12 61 0.8× 43 0.7× 39 0.7× 129 2.4× 102 2.1× 27 390
Vincenzo Salpietro Italy 9 102 1.4× 51 0.8× 12 0.2× 50 0.9× 39 0.8× 12 360

Countries citing papers authored by Elif Özsu

Since Specialization
Citations

This map shows the geographic impact of Elif Özsu'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 Elif Özsu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elif Özsu more than expected).

Fields of papers citing papers by Elif Özsu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elif Özsu. 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 Elif Özsu. The network helps show where Elif Özsu may publish in the future.

Co-authorship network of co-authors of Elif Özsu

This figure shows the co-authorship network connecting the top 25 collaborators of Elif Özsu. A scholar is included among the top collaborators of Elif Özsu 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 Elif Özsu. Elif Özsu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
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.
3.
Berberoğlu, Merih, et al.. (2024). Assessment of the Admission and Follow-up Characteristics of Children Diagnosed with Secondary Osteoporosis. Journal of Clinical Research in Pediatric Endocrinology. 16(4). 466–474.
4.
Joustra, Sjoerd D., Jan M. Wit, Gönül Çatlı, et al.. (2024). Genetic Findings in Short Turkish Children Born to Consanguineous Parents. Hormone Research in Paediatrics. 98(5). 532–542.
5.
Özen, Samim, Semra Çeti̇nkaya, Leyla Akın, et al.. (2023). A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review. The Journal of Clinical Endocrinology & Metabolism. 108(9). 2371–2388. 7 indexed citations
6.
Şıklar, Zeynep, et al.. (2023). Clinical Characteristics and Treatment Outcomes of Children with Primary Osteoporosis. Turkish Archives of Pediatrics. 58(3). 314–321. 2 indexed citations
7.
Şıklar, Zeynep, et al.. (2023). Clinical Profile of Parathyroid Adenoma in Children and Adolescents: A Single-Center Experience. Turkish Archives of Pediatrics. 58(1). 56–61. 2 indexed citations
8.
Çeti̇nkaya, Semra, et al.. (2023). Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasia. Clinical Endocrinology. 99(2). 135–141.
9.
Şıklar, Zeynep, et al.. (2022). Fibroblast Growth Factor 21 Levels and Bone Mineral Density in Metabolically Healthy and Metabolically Unhealthy Obese Children. Journal of Clinical Research in Pediatric Endocrinology. 14(4). 433–443. 4 indexed citations
10.
Eminoğlu, Fatma Tuba, et al.. (2021). Serum biotin interference: A troublemaker in hormone immunoassays. Clinical Biochemistry. 99. 97–102. 5 indexed citations
11.
Okulu, Emel, et al.. (2020). A Newborn with Bilateral Breast Enlargement: Neonatal Mastauxe. SHILAP Revista de lepidopterología. 73(3). 312–314.
12.
Özsu, Elif, et al.. (2020). A Rare Cause of Sleep-Disordered Breathing: ROHHAD Syndrome. Frontiers in Pediatrics. 8. 573227–573227. 5 indexed citations
13.
Şıklar, Zeynep, Çiğdem Soydal, Elif Özsu, et al.. (2020). Treatment Management with 18F-Fluoro-L-DOPA PET/CT Imaging of Focal Congenital Hyperinsulinemic Hypoglycemia Case. 29(3). 187–194.
14.
15.
Özsu, Elif, Gül Yeşiltepe Mutlu, Filiz Çizmecioğlu, & Şükrü Hatun. (2015). McCune Albright syndrome in association with excessive GH secretion: case report. Türk Pediatri Arşivi. 50(2). 114–117. 3 indexed citations
16.
Özsu, Elif, et al.. (2014). Features of Two Cases with 18q Deletion Syndrome. Journal of Clinical Research in Pediatric Endocrinology. 6(1). 51–54. 8 indexed citations
17.
Mutlu, Gül Yeşiltepe, Heves Kırmızıbekmez, Elif Özsu, İlkay Er, & Şükrü Hatun. (2014). Metabolic Bone Disease of Prematurity: Report of Four Cases. Journal of Clinical Research in Pediatric Endocrinology. 6(2). 111–115. 13 indexed citations
18.
Özsu, Elif, et al.. (2014). Ring Chromosome 13 and Ambiguous Genitalia. Journal of Clinical Research in Pediatric Endocrinology. 6(2). 122–124. 4 indexed citations
19.
Mutlu, Gül Yeşiltepe, et al.. (2011). Prevention of Vitamin D deficiency in infancy: daily 400 IU vitamin D is sufficient. International Journal of Pediatric Endocrinology. 2011(1). 4–4. 34 indexed citations
20.
Genel, Ferah, et al.. (2009). Monocyte HLA-DR expression as predictor of poor outcome in neonates with late onset neonatal sepsis. Journal of Infection. 60(3). 224–228. 47 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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