Özlem Sezer

701 total citations
35 papers, 150 citations indexed

About

Özlem Sezer is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Özlem Sezer has authored 35 papers receiving a total of 150 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 7 papers in Immunology. Recurrent topics in Özlem Sezer's work include Inflammasome and immune disorders (5 papers), COVID-19 Clinical Research Studies (4 papers) and Vitamin D Research Studies (3 papers). Özlem Sezer is often cited by papers focused on Inflammasome and immune disorders (5 papers), COVID-19 Clinical Research Studies (4 papers) and Vitamin D Research Studies (3 papers). Özlem Sezer collaborates with scholars based in Türkiye, Canada and Taiwan. Özlem Sezer's co-authors include Serbülent Yi̇ği̇t, Özgür Günal, Mehmet Derya Demirağ, Ahmet Şen, Süleyman Sırrı KILIÇ, Rauf Taner Di̇vri̇k, Ebru Çakır, Ümit Bayol, Serdar Ceylaner and Emel Ebru Pala and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Scandinavian Journal of Clinical and Laboratory Investigation.

In The Last Decade

Özlem Sezer

28 papers receiving 148 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Özlem Sezer Türkiye 7 41 39 38 24 19 35 150
Eoin O’Connor Spain 4 24 0.6× 9 0.2× 49 1.3× 11 0.5× 14 0.7× 6 107
Víctor Acuña-Alonzo Mexico 6 36 0.9× 87 2.2× 33 0.9× 25 1.0× 9 0.5× 8 224
Johann Rahmöller Germany 5 65 1.6× 72 1.8× 35 0.9× 11 0.5× 11 0.6× 6 170
Florian Fronhoffs Germany 6 108 2.6× 40 1.0× 5 0.1× 36 1.5× 29 1.5× 11 214
Victoria Connor United Kingdom 7 18 0.4× 29 0.7× 16 0.4× 6 0.3× 9 0.5× 8 137
John Widdrington United Kingdom 6 30 0.7× 28 0.7× 46 1.2× 43 1.8× 12 0.6× 7 163
G. Monasterolo Italy 15 34 0.8× 49 1.3× 9 0.2× 9 0.4× 11 0.6× 25 566
Koen van Aerde Netherlands 7 133 3.2× 27 0.7× 8 0.2× 85 3.5× 14 0.7× 22 255
Janina Petry Germany 2 45 1.1× 72 1.8× 15 0.4× 9 0.4× 9 0.5× 3 124
Sian Kirkham United Kingdom 9 63 1.5× 36 0.9× 8 0.2× 49 2.0× 9 0.5× 13 234

Countries citing papers authored by Özlem Sezer

Since Specialization
Citations

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

Fields of papers citing papers by Özlem Sezer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Özlem Sezer

This figure shows the co-authorship network connecting the top 25 collaborators of Özlem Sezer. A scholar is included among the top collaborators of Özlem Sezer 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 Özlem Sezer. Özlem Sezer 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.
Sezer, Özlem, et al.. (2025). The frequency of JAK2 V617F mutation and its association with low EPO levels in polycythemia vera patients. Scandinavian Journal of Clinical and Laboratory Investigation. 85(4). 259–262.
3.
4.
Sezer, Özlem, et al.. (2024). Hyperekplexia: A Single-Center Experience. Journal of Child Neurology. 39(7-8). 260–267. 1 indexed citations
5.
Sezer, Özlem, et al.. (2023). Evaluating interleukin-6 levels and the rs1800795 variant in Turkish patients with COVID-19: a prospective cohort study. Nucleosides Nucleotides & Nucleic Acids. 43(4). 377–390. 1 indexed citations
6.
Yi̇ği̇t, Serbülent, et al.. (2023). Clock 3111 T/C and Period3 VNTR gene polymorphisms and proteins, and melatonin levels in women with infertility. Journal of Assisted Reproduction and Genetics. 40(5). 1109–1116. 1 indexed citations
7.
Dahan, Michael H., Özlem Sezer, Alper Başbuğ, et al.. (2023). TUBB8 mutations as a cause of oocyte maturation abnormalities: presentation of oocyte and embryo profiles and novel mutations. Reproductive BioMedicine Online. 47(5). 103257–103257. 2 indexed citations
8.
Yi̇ği̇t, Serbülent, et al.. (2023). Effect of vitamin D receptor gene BsmI polymorphism on hospitalization of SARS-CoV-2 positive patients. Nucleosides Nucleotides & Nucleic Acids. 43(3). 264–275. 1 indexed citations
9.
Sezer, Özlem, et al.. (2023). YIF1B-related Kaya-Barakat-Masson Syndrome: Report of a new patient and literature review. European Journal of Medical Genetics. 66(6). 104751–104751. 1 indexed citations
10.
Hatırnaz, Şafak, Aşkı Ellibeş Kaya, Özlem Sezer, et al.. (2022). Oocyte maturation abnormalities - A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina. Journal of Turkish Society of Obstetric and Gynecology. 19(1). 60–80. 11 indexed citations
11.
Sezer, Özlem, et al.. (2022). Possible effect of genetic background in thrombophilia genes on clinical severity of patients with coronavirus disease-2019: A prospective cohort study. SHILAP Revista de lepidopterología. 3(3). 183–199. 1 indexed citations
12.
Türkmen, Ercan, et al.. (2018). Angiotensin Converting Enzyme Gene Insertion/Deletion Variant and Familial Mediterranean Fever-related Amyloidosis.. PubMed. 12(3). 150–155. 3 indexed citations
13.
Günal, Özgür, Serbülent Yi̇ği̇t, Arzu Didem Yalçın, et al.. (2016). The IL4-VNTR P1 Allele, IL4-VNTR P2P2 Genotype, and IL4-VNTR_IL6-174CG P2P1-GG Genotype Are Associated with an Increased Risk of Brucellosis. Japanese Journal of Infectious Diseases. 70(1). 61–64. 4 indexed citations
14.
Sezer, Özlem, et al.. (2016). Interleukin-1Ra rs2234663 and Interleukin-4 rs79071878 Polymorphisms in Familial Mediterranean Fever. Gene. 582(2). 173–177. 6 indexed citations
15.
Mete, Türkan, et al.. (2015). Association between colchicine resistance and vitamin D in familial Mediterranean fever. Renal Failure. 37(7). 1122–1125. 12 indexed citations
16.
Pala, Emel Ebru, et al.. (2015). Problems In Determining Her2 Status In Breast Carcinoma. SHILAP Revista de lepidopterología. 11(1). 10–16. 1 indexed citations
17.
Pala, Emel Ebru, Ebru Çakır, Özlem Sezer, et al.. (2015). Clınical, demographic and histopathological prognostic factors for urothelial carcinoma of the bladder. Editor-in-Chief s Voice List of Authors is an Important Element in a Scientific Publication. 68(1). 30–6. 14 indexed citations
18.
Küçük, Uğur, et al.. (2015). Significance of TNM staging, Demographic and Histologic Features in Predicting the Prognosis of Renal Cell Carcinoma. Acta Chirurgica Belgica. 115(3). 202–207. 5 indexed citations
19.
Sezer, Özlem, et al.. (2014). Fibular aplasia, tibial campomelia, and oligosyndactyly. Clinical Dysmorphology. 23(4). 121–126. 8 indexed citations
20.
Güneş, Sezgin, et al.. (2008). 45,X/46,X,i(Xq) Karyotipe Sahip İki Mozaik Turner Sendromu Olgusu. Turkiye Klinikleri Tip Bilimleri Dergisi. 28(2). 236–238.

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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