Ajlan Tükün

1.2k total citations
54 papers, 902 citations indexed

About

Ajlan Tükün is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Ajlan Tükün has authored 54 papers receiving a total of 902 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Physiology. Recurrent topics in Ajlan Tükün's work include Telomeres, Telomerase, and Senescence (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Sexual Differentiation and Disorders (5 papers). Ajlan Tükün is often cited by papers focused on Telomeres, Telomerase, and Senescence (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Sexual Differentiation and Disorders (5 papers). Ajlan Tükün collaborates with scholars based in Türkiye, United States and United Kingdom. Ajlan Tükün's co-authors include Güvem Gümüş‐Akay, Serçin Karahüseyinoğlu, Duygu Özel Demiralp, Duygu Uçkan, Fadıl Kara, Alp Can, Emine Kılıç, Atilla Halil Elhan, Halil Gürhan Karabulut and Sena Aydos and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Ajlan Tükün

51 papers receiving 868 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ajlan Tükün Türkiye 14 374 339 272 108 100 54 902
Audrey Cras France 19 352 0.9× 421 1.2× 181 0.7× 56 0.5× 153 1.5× 43 950
Veronica Lisi Italy 14 619 1.7× 418 1.2× 267 1.0× 61 0.6× 93 0.9× 29 1.2k
Shlomo Bulvik Israel 18 548 1.5× 461 1.4× 343 1.3× 133 1.2× 89 0.9× 32 1.3k
Nayoun Kim South Korea 18 562 1.5× 313 0.9× 232 0.9× 74 0.7× 116 1.2× 40 1.1k
Cathérine Henry France 14 354 0.9× 504 1.5× 192 0.7× 262 2.4× 85 0.8× 23 1.0k
Stefania Crippa Italy 21 421 1.1× 892 2.6× 351 1.3× 76 0.7× 121 1.2× 46 1.5k
Yumi Fukuchi Japan 19 487 1.3× 748 2.2× 292 1.1× 74 0.7× 265 2.6× 39 1.5k
Hyun Hwa Cho South Korea 18 693 1.9× 703 2.1× 337 1.2× 70 0.6× 46 0.5× 20 1.5k
Mika Wada Japan 18 242 0.6× 497 1.5× 231 0.8× 60 0.6× 67 0.7× 32 920
Valerie D. Roobrouck Belgium 13 503 1.3× 322 0.9× 346 1.3× 51 0.5× 51 0.5× 20 897

Countries citing papers authored by Ajlan Tükün

Since Specialization
Citations

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

Fields of papers citing papers by Ajlan Tükün

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ajlan Tükün

This figure shows the co-authorship network connecting the top 25 collaborators of Ajlan Tükün. A scholar is included among the top collaborators of Ajlan Tükün 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 Ajlan Tükün. Ajlan Tükün 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.
Topçuoğlu, Mehmet Akif, et al.. (2021). The association between telomere length and ischemic stroke risk and phenotype. Scientific Reports. 11(1). 10967–10967. 13 indexed citations
2.
Tükün, Ajlan, et al.. (2020). Vitamin D receptor polymorphisms and bone health after kidney transplantation. TURKISH JOURNAL OF MEDICAL SCIENCES. 51(2). 802–812. 5 indexed citations
3.
4.
Doğan, Mutlu, et al.. (2015). Molecular Spectrum of PIK3CA Gene Mutations in Patients with Nonsmall-Cell Lung Cancer in Turkey. Genetic Testing and Molecular Biomarkers. 19(7). 353–358. 4 indexed citations
5.
Öçal, Gönül, Merih Berberoğlu, Zeynep Şıklar, et al.. (2014). Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification. Journal of Pediatric and Adolescent Gynecology. 28(1). 6–11. 15 indexed citations
6.
Hazan, Fılız, et al.. (2013). A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.. PubMed. 19. 196–202. 13 indexed citations
7.
Hazan, Fılız, et al.. (2012). Hypochondroplasia in a Child With 1620c>G (Asn540lys) Mutation in FGFR3. Journal of Clinical Research in Pediatric Endocrinology. 4(4). 220–2. 5 indexed citations
8.
Doğan, Mutlu, Halil Gürhan Karabulut, Ajlan Tükün, et al.. (2012). Relationship Between Antimetabolite Toxicity and Pharmacogenetics in Turkish Cancer Patients. Asian Pacific Journal of Cancer Prevention. 13(4). 1553–1556. 8 indexed citations
9.
Öçal, Gönül, Merih Berberoğlu, Zeynep Şıklar, et al.. (2012). The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?. European Journal of Pediatrics. 171(10). 1497–1502. 18 indexed citations
10.
Tükün, Ajlan, et al.. (2011). Meme kanserinde risk faktörleri, riskin değerlendirilmesi ve prevansiyon: İstanbul 2010 konsensus raporu. 7(2). 47–67. 6 indexed citations
11.
Ekız, Fuat, Necati Örmecı, Şahin Çoban, et al.. (2011). Association of methylenetetrahydrofolate reductase C677T-A1298C polymorphisms with risk for esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis. Diseases of the Esophagus. 25(5). 437–441. 8 indexed citations
12.
13.
Olcay, Lale, et al.. (2010). A Child With Myelodysplastic Syndrome With Hypocellular Fibrosis. Journal of Pediatric Hematology/Oncology. 32(8). 617–620. 2 indexed citations
14.
Polat, Onur, et al.. (2009). Bone Fracture Healing with Umbilico-Placental Mononuclear Cells: A Controlled Animal Study. European Journal of Trauma and Emergency Surgery. 36(1). 60–66. 1 indexed citations
15.
Gümüş‐Akay, Güvem, Atilla Halil Elhan, Ali Ekrem Ünal, et al.. (2009). Effects of Genomic Imbalances on Telomerase Activity in Gastric Cancer: Clues to Telomerase Regulation. Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics. 17(10). 455–462. 3 indexed citations
16.
Sadeghi, Fatemeh, Merih Berberoğlu, Zehra Aycan, et al.. (2008). Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey. Journal of Pediatric Endocrinology and Metabolism. 21(8). 781–7. 25 indexed citations
17.
Topçuoğlu, Pervin, et al.. (2006). Translocation (13;17)(q14;q25) as a novel chromosomal abnormality in acute myeloid leukemia-M4. Leukemia Research. 30(7). 903–905. 4 indexed citations
18.
Tükün, Ajlan, et al.. (2005). The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey. European Journal of Medical Genetics. 48(1). 13–19. 4 indexed citations
19.
Aydos, Sena, Atilla Halil Elhan, & Ajlan Tükün. (2005). Is telomere length one of the determinants of reproductive life span?. Archives of Gynecology and Obstetrics. 272(2). 113–116. 50 indexed citations
20.
Tükün, Ajlan, et al.. (2000). Mental retardation with rare fragile site expressed at 2q11. Brain and Development. 22(8). 498–500. 3 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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