Sacide Pehlıvan

1.6k total citations
137 papers, 1.1k citations indexed

About

Sacide Pehlıvan is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, Sacide Pehlıvan has authored 137 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 33 papers in Immunology and 20 papers in Oncology. Recurrent topics in Sacide Pehlıvan's work include Tryptophan and brain disorders (9 papers), Epigenetics and DNA Methylation (9 papers) and Cannabis and Cannabinoid Research (9 papers). Sacide Pehlıvan is often cited by papers focused on Tryptophan and brain disorders (9 papers), Epigenetics and DNA Methylation (9 papers) and Cannabis and Cannabinoid Research (9 papers). Sacide Pehlıvan collaborates with scholars based in Türkiye, Antigua and Barbuda and Cambodia. Sacide Pehlıvan's co-authors include Mustafa Pehlıvan, Ferda Özkınay, Sibel Oğuzkan Balcı, Hüseyin Önay, Cihangir Özkınay, Vahap Okan, Ziya Kırkalı, M. Yılmaz, Meral Koyuncuoğlu and Ayşe Balat and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Plastic & Reconstructive Surgery.

In The Last Decade

Sacide Pehlıvan

124 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sacide Pehlıvan Türkiye 18 330 300 143 137 107 137 1.1k
Ghasem Solgi Iran 20 291 0.9× 392 1.3× 128 0.9× 162 1.2× 100 0.9× 93 1.3k
Min Kyoung Kim South Korea 17 227 0.7× 163 0.5× 146 1.0× 208 1.5× 77 0.7× 62 932
Mustafa Pehlıvan Türkiye 17 219 0.7× 189 0.6× 204 1.4× 180 1.3× 41 0.4× 117 867
Babs O. Fabriek Netherlands 12 297 0.9× 574 1.9× 50 0.3× 102 0.7× 105 1.0× 13 1.4k
Tzu Phang United States 21 529 1.6× 201 0.7× 90 0.6× 199 1.5× 189 1.8× 40 1.3k
Marı́a-Luisa Gaspar Spain 21 395 1.2× 471 1.6× 71 0.5× 108 0.8× 134 1.3× 53 1.2k
Mónica Martínez‐Gallo Spain 20 210 0.6× 481 1.6× 60 0.4× 65 0.5× 177 1.7× 77 1.2k
Walter Sibrowski Germany 22 470 1.4× 156 0.5× 331 2.3× 157 1.1× 85 0.8× 109 1.5k
Mary M. DeSouza United States 15 229 0.7× 473 1.6× 102 0.7× 52 0.4× 87 0.8× 22 1.2k

Countries citing papers authored by Sacide Pehlıvan

Since Specialization
Citations

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

Fields of papers citing papers by Sacide Pehlıvan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sacide Pehlıvan

This figure shows the co-authorship network connecting the top 25 collaborators of Sacide Pehlıvan. A scholar is included among the top collaborators of Sacide Pehlıvan 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 Sacide Pehlıvan. Sacide Pehlıvan 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.
Pehlıvan, Mustafa, et al.. (2024). The effect of leptin gene polymorphisms (LEP rs7799039 and LEPR rs1137101) on febrile neutropenia. Heliyon. 10(7). e28788–e28788. 1 indexed citations
2.
Pehlıvan, Sacide, Mustafa Pehlıvan, Gözde Yeşil, et al.. (2023). The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course. Nucleosides Nucleotides & Nucleic Acids. 42(8). 571–585. 3 indexed citations
3.
Pehlıvan, Mustafa, et al.. (2023). Genetic polymorphism of IL-17F rs763780 contributes to the susceptibility to bipolar disorder but not to schizophrenia in the Turkish population. Nucleosides Nucleotides & Nucleic Acids. 42(11). 852–866. 4 indexed citations
4.
Pehlıvan, Mustafa, et al.. (2023). Effect of interleukin-2 (IL-2) polymorphisms on multiple myeloma: IL-2RA rs2104286, IL-2 rs2069762 and rs2069763 polymorphisms. Cytokine. 172. 156401–156401. 1 indexed citations
5.
Köse, Murat, Mustafa Önel, Gözde Yeşil, et al.. (2023). ASSOCIATING eNOS GENE VARIANTS WITH COVID-19 SUSCEPTIBILITY IN THE TURKISH POPULATION. SHILAP Revista de lepidopterología. 86(1). 1–6. 1 indexed citations
6.
Pehlıvan, Sacide, et al.. (2022). Quantitative detection of methylated SOCS-1 in schizophrenia and bipolar disorder considering SOCS-1 -1478CA/del polymorphism and clinical parameters. Irish Journal of Medical Science (1971 -). 192(2). 775–783. 4 indexed citations
7.
Tükek, Tufan, et al.. (2022). The suppressor of cytokine signaling-1 ( SOCS1 ) gene polymorphism and promoter methylation correlate with the course of COVID-19. Pathogens and Global Health. 117(4). 392–400. 2 indexed citations
8.
Özdilli, Kürşat, et al.. (2022). Cytokine gene polymorphism frequencies in Turkish population living in Marmara region. SHILAP Revista de lepidopterología. 47(5). 580–587.
9.
Pehlıvan, Sacide, et al.. (2021). Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (–) patients. Pathogens and Global Health. 116(3). 178–184. 7 indexed citations
10.
Pehlıvan, Mustafa, et al.. (2021). DNA Methylation Pattern of Gene Promoters of MB-COMT, DRD2, and NR3C1 in Turkish Patients Diagnosed with Schizophrenia. Clinical Psychopharmacology and Neuroscience. 20(4). 685–693. 8 indexed citations
11.
12.
Pehlıvan, Sacide, et al.. (2021). What are the roles of global DNA and APC 2 gene promotor hypermethylation in multiple myeloma?. Molecular Biology Reports. 48(12). 7875–7882. 5 indexed citations
13.
Pehlıvan, Sacide, et al.. (2020). Viral Pandemics as Possible Psycho-immunological Causes of Psychiatric Symptoms: From Past to Present. 3(1). 92–98. 1 indexed citations
14.
Pehlıvan, Mustafa, et al.. (2020). The miRNA 196a2 rs11614913 variant has prognostic impact on Turkish patients with multiple myeloma. BMC Research Notes. 13(1). 545–545. 2 indexed citations
15.
Özdilli, Kürşat, et al.. (2020). Tumor Necrosis Factor-alpha (TNF-α) −238 G/A Polymorphism Is Associated with the Treatment Resistance and Attempted Suicide in Schizophrenia. Immunological Investigations. 51(2). 368–380. 16 indexed citations
16.
Pehlıvan, Mustafa, et al.. (2020). Role of MIF-173G/C and Mbl2 Codon 54A/B Variants in the Risk of Multiple Myeloma: An Association Study. Endocrine Metabolic & Immune Disorders - Drug Targets. 21(5). 925–931. 1 indexed citations
17.
Pehlıvan, Sacide, Ali Aydeniz, Özlem Altındağ, et al.. (2016). The functional variants of endothelial nitric oxide synthase gene associated with rheumatoid arthritis in Turkish adults. Clinical Rheumatology. 36(3). 537–540. 3 indexed citations
18.
Aydeniz, Ali, et al.. (2011). Investigation of Glucocorticoid Receptor Gene Bcl-1 Polymorphism in Rheumatoid Arthritis. Archives of Rheumatology. 26(3). 199–203. 2 indexed citations
19.
Ercıyas, Kamile, Sacide Pehlıvan, Mehri İğci, et al.. (2010). Endothelial nitric oxide synthase gene polymorphisms associated with periodontal diseases in Turkish adults. AFRICAN JOURNAL OF BIOTECHNOLOGY. 9(21). 3042–3047. 11 indexed citations
20.
Pehlıvan, Sacide, et al.. (2008). Angiotensin Converting Enzyme Gene Polymorphisms In Male Infertility. European Journal of Therapeutics. 14(2). 15–17.

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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