Sultan Cingöz

421 total citations
18 papers, 254 citations indexed

About

Sultan Cingöz is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Sultan Cingöz has authored 18 papers receiving a total of 254 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Surgery. Recurrent topics in Sultan Cingöz's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Regulation of Appetite and Obesity (3 papers). Sultan Cingöz is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Regulation of Appetite and Obesity (3 papers). Sultan Cingöz collaborates with scholars based in Türkiye, United States and Denmark. Sultan Cingöz's co-authors include Meral Sakızlı, Nazan Uysal, İlkay Aksu, Ayfer Dayı, Tülay Canda, Gazanfer Aksakoğlu, Serdar Saydam, Ziya Kırkalı, Müge Kıray and Celal Gençoğlu and has published in prestigious journals such as Cancer Letters, BMC Cancer and The Scientific World JOURNAL.

In The Last Decade

Sultan Cingöz

18 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sultan Cingöz Türkiye 10 99 60 46 36 31 18 254
Kotaro Yuge Japan 10 109 1.1× 40 0.7× 17 0.4× 72 2.0× 32 1.0× 35 295
Raffaele Gerlini Germany 10 116 1.2× 29 0.5× 28 0.6× 18 0.5× 17 0.5× 15 210
Rita Holdhus Norway 8 153 1.5× 66 1.1× 64 1.4× 24 0.7× 10 0.3× 9 308
Kathleen J. Krentz United States 9 145 1.5× 74 1.2× 67 1.5× 47 1.3× 24 0.8× 13 396
Luca Pagliaroli Hungary 8 206 2.1× 36 0.6× 54 1.2× 29 0.8× 11 0.4× 11 352
Naoko Tsukamoto Japan 13 200 2.0× 67 1.1× 25 0.5× 25 0.7× 31 1.0× 18 405
Evan M. Lutton United States 9 200 2.0× 53 0.9× 25 0.5× 18 0.5× 26 0.8× 9 393
Kirti Chaturvedi United States 13 363 3.7× 39 0.7× 44 1.0× 40 1.1× 23 0.7× 24 529
Martina Winklmayr Austria 9 213 2.2× 37 0.6× 21 0.5× 32 0.9× 12 0.4× 12 344
Xiameng Chen China 13 112 1.1× 21 0.3× 45 1.0× 12 0.3× 33 1.1× 29 263

Countries citing papers authored by Sultan Cingöz

Since Specialization
Citations

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

Fields of papers citing papers by Sultan Cingöz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sultan Cingöz

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

All Works

18 of 18 papers shown
1.
Cingöz, Sultan, Ezgi Karaca, Burcu Çelet Özden, et al.. (2022). Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations. European Journal of Medical Genetics. 65(6). 104497–104497. 1 indexed citations
2.
3.
Yüksel, Bayram, et al.. (2018). GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria. The Turkish Journal of Pediatrics. 60(3). 229–237. 8 indexed citations
4.
Uysal, Nazan, Ali Rıza Şişman, Ulaş Mehmet Çamsarı, et al.. (2017). Exercise increases leptin levels correlated with IGF-1 in hippocampus and prefrontal cortex of adolescent male and female rats. Journal of Chemical Neuroanatomy. 81. 27–33. 24 indexed citations
5.
Cingöz, Sultan, et al.. (2014). Identification of the Variations in the CPT1B and CHKB Genes Along with the HLA-DQB1*06:02 Allele in Turkish Narcolepsy Patients and Healthy Persons. Genetic Testing and Molecular Biomarkers. 18(4). 261–268. 7 indexed citations
6.
Yörükoğlu, Kutsal, et al.. (2013). The effect of the alternative solutions to formaldehyde and xylene on tissue processing. Indian Journal of Pathology and Microbiology. 56(3). 221–221. 7 indexed citations
7.
Ateş, Mehmet, Ayfer Dayı, Müge Kıray, et al.. (2013). Anxiety- and depression-like behavior are correlated with leptin and leptin receptor expression in prefrontal cortex of streptozotocin-induced diabetic rats. Biotechnic & Histochemistry. 89(3). 161–171. 24 indexed citations
8.
Cokol, Murat, et al.. (2012). Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α. BMC Cancer. 12(1). 450–450. 22 indexed citations
9.
10.
Dayı, Ayfer, Seda Özbal, Ferihan Çeti̇n, et al.. (2012). Maternal Aerobic Exercise during Pregnancy Can Increase Spatial Learning by Affecting Leptin Expression on Offspring's Early and Late Period in Life Depending on Gender. The Scientific World JOURNAL. 2012. 1–8. 34 indexed citations
11.
12.
Cingöz, Sultan, Iben Bache, Hans‐Hilger Ropers, et al.. (2010). Interstitial deletion of 14q24.3‐q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects. American Journal of Medical Genetics Part A. 155(1). 203–206. 6 indexed citations
13.
Soylu, Alper, Sefa Kızıldağ, Salìh Kavukçu, et al.. (2009). TLR-2 Arg753Gln, TLR-4 Asp299Gly, and TLR-4 Thr399Ile polymorphisms in Henoch Schonlein purpura with and without renal involvement. Rheumatology International. 30(5). 667–670. 18 indexed citations
14.
Cingöz, Sultan, Behzat Özkan, Hakan Döneray, & Meral Sakızlı. (2007). Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11β-hydroxylase deficiency. Journal of Endocrinological Investigation. 30(4). 285–291. 6 indexed citations
15.
Cingöz, Sultan, Anne‐Marie Bisgaard, Iben Bache, et al.. (2006). 4q35 deletion and 10p15 duplication associated with immunodeficiency. American Journal of Medical Genetics Part A. 140A(20). 2231–2235. 9 indexed citations
16.
Tümer, Zeynep, Helle Hjalgrim, Johanne M D Hahnemann, et al.. (2005). Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter. BMC Medical Genetics. 6(1). 21–21. 21 indexed citations
17.
Cingöz, Sultan, et al.. (2003). DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors. Cancer Genetics and Cytogenetics. 145(2). 108–114. 33 indexed citations
18.
Koyuncuoğlu, Meral, Aydanur Kargı, Sultan Cingöz, & Ziya Kırkalı. (1998). Investigation of p53, c-erbB-2, PCNA immunoreactivity, DNA content, AgNOR and apoptosis in bladder carcinoma as prognostic parameters. Cancer Letters. 126(2). 143–148. 18 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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