Şehime Gülsün Temel

1.7k total citations
62 papers, 540 citations indexed

About

Şehime Gülsün Temel is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Şehime Gülsün Temel has authored 62 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 20 papers in Genetics and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Şehime Gülsün Temel's work include RNA modifications and cancer (6 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (4 papers). Şehime Gülsün Temel is often cited by papers focused on RNA modifications and cancer (6 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (4 papers). Şehime Gülsün Temel collaborates with scholars based in Türkiye, Cyprus and United Kingdom. Şehime Gülsün Temel's co-authors include Tuncay Küsbeci, Berkant Kaderli, Remzi Avcı, Berrin Avcı, Mahmut Çerkez Ergören, Özgür Kütük, Şahsine Tolunay, Hüveyda Başağa, Lothar Jennes and Tülin Alkan and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Şehime Gülsün Temel

55 papers receiving 526 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Şehime Gülsün Temel Türkiye 13 244 111 92 76 56 62 540
Bibiana Moreno-Carranza Mexico 12 151 0.6× 55 0.5× 64 0.7× 44 0.6× 24 0.4× 18 457
Bo Ma China 19 333 1.4× 44 0.4× 254 2.8× 153 2.0× 26 0.5× 56 762
Zachariah G. Goldsmith United States 12 294 1.2× 25 0.2× 41 0.4× 74 1.0× 22 0.4× 23 742
Takahisa Koga Japan 16 301 1.2× 35 0.3× 356 3.9× 161 2.1× 23 0.4× 24 651
Chang-Jun Zhang China 13 308 1.3× 45 0.4× 87 0.9× 39 0.5× 8 0.1× 26 677
Scott Sayers United States 12 196 0.8× 28 0.3× 47 0.5× 18 0.2× 84 1.5× 30 587
Teng He China 12 259 1.1× 13 0.1× 94 1.0× 56 0.7× 60 1.1× 24 543
Juan E. Gallo Argentina 17 130 0.5× 24 0.2× 209 2.3× 361 4.8× 31 0.6× 43 721
Takahisa Noto Japan 17 280 1.1× 29 0.3× 20 0.2× 16 0.2× 28 0.5× 47 636

Countries citing papers authored by Şehime Gülsün Temel

Since Specialization
Citations

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

Fields of papers citing papers by Şehime Gülsün Temel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Şehime Gülsün Temel. 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 Şehime Gülsün Temel. The network helps show where Şehime Gülsün Temel may publish in the future.

Co-authorship network of co-authors of Şehime Gülsün Temel

This figure shows the co-authorship network connecting the top 25 collaborators of Şehime Gülsün Temel. A scholar is included among the top collaborators of Şehime Gülsün Temel 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 Şehime Gülsün Temel. Şehime Gülsün Temel 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.
Ji, Weizhen, Saquib A. Lakhani, Fatma Sılan, et al.. (2024). CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life Science Alliance. 7(10). e202402708–e202402708. 2 indexed citations
2.
Karpat, Fatih, et al.. (2024). Investigation of infectious droplet dispersion in a hospital examination room cooled by split-type air conditioner. Journal of Environmental Health Science and Engineering. 22(2). 471–482.
3.
Altay, Özlem, et al.. (2024). Identifying Hub Genes and Metabolic Pathways in Collagen VI-Related Dystrophies: A Roadmap to Therapeutic Intervention. Biomolecules. 14(11). 1376–1376. 2 indexed citations
4.
Eren, Erdal, et al.. (2024). Genotype and Phenotype Correlation of Patients with Osteogenesis Imperfecta. Journal of Molecular Diagnostics. 26(9). 754–769. 2 indexed citations
5.
Eren, Erdal, et al.. (2023). A Novel PHEX Mutation in A Case Followed Up with A Diagnosis of X-linked Hypophosphatemic Rickets. Güncel Pediatri. 21(1). 98–101.
6.
Kubar, Ayhan, Şehime Gülsün Temel, Serdar Beken, et al.. (2023). A new line method; A direct test in spinal muscular atrophy screening for DBS. Molecular Genetics & Genomic Medicine. 11(12). e2270–e2270. 1 indexed citations
7.
8.
Ergören, Mahmut Çerkez, et al.. (2022). Structural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility. PeerJ. 10. e12947–e12947. 3 indexed citations
9.
Bişgin, Atıl, et al.. (2022). Nanobubble Ozone Stored in Hyaluronic Acid Decorated Liposomes: Antibacterial, Anti-SARS-CoV-2 Effect and Biocompatibility Tests. Dove Medical Press (Taylor and Francis Group). 9 indexed citations
10.
Temel, Şehime Gülsün, et al.. (2021). Mitochondrial estrogen receptors alter mitochondrial priming and response to endocrine therapy in breast cancer cells. Cell Death Discovery. 7(1). 189–189. 10 indexed citations
11.
Demır, Selma, Emine İkbal Atlı, Ruken Yıldırım, et al.. (2021). Targeted High-Throughput Sequencing Analysis Results of Osteogenesis Imperfecta Patients from Different Regions of Turkey. Genetic Testing and Molecular Biomarkers. 25(1). 59–67. 2 indexed citations
12.
Temel, Şehime Gülsün, et al.. (2021). BRCA Variations Risk Assessment in Breast Cancers Using Different Artificial Intelligence Models. Genes. 12(11). 1774–1774. 3 indexed citations
13.
14.
Temel, Şehime Gülsün, Mahmut Çerkez Ergören, Elena Manara, et al.. (2020). Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann–Rautenstrauch syndrome. European Journal of Human Genetics. 28(12). 1675–1680. 7 indexed citations
15.
Ergören, Mahmut Çerkez, et al.. (2020). A rare case of fructose-1,6-bisphosphatase deficiency: a delayed diagnosis story. Turkish Journal of Biochemistry. 45(5). 613–616. 3 indexed citations
16.
Temel, Şehime Gülsün, et al.. (2019). Strong association between VDR FokI (rs2228570) gene variant and serum vitamin D levels in Turkish Cypriots. Molecular Biology Reports. 46(3). 3349–3355. 23 indexed citations
17.
Temel, Şehime Gülsün, et al.. (2018). The use of ACE INDEL polymorphism as a biomarker of coronary artery disease (CAD) in humans with Mediterranean-style diet. International Journal of Biological Macromolecules. 123. 576–580. 3 indexed citations
18.
Kütük, Özgür, Şehime Gülsün Temel, Şahsine Tolunay, & Hüveyda Başağa. (2010). Aven blocks DNA damage-induced apoptosis by stabilising Bcl-xL. European Journal of Cancer. 46(13). 2494–2505. 28 indexed citations
19.
Temel, Şehime Gülsün, et al.. (2006). Extended Pedigree with Multiple Cases of XX Sex Reversal in the Absence of <i>SRY</i> and of a Mutation at the <i>SOX9</i> Locus. Sexual Development. 1(1). 24–34. 29 indexed citations
20.
Temel, Şehime Gülsün, et al.. (2001). Rapid Polymerisation with Microwave Irradiation for Transmission Electron Microscopy. European Journal of Morphology. 39(5). 313–317. 8 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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