Yusuf Tunca

535 total citations
30 papers, 270 citations indexed

About

Yusuf Tunca is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Yusuf Tunca has authored 30 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Immunology. Recurrent topics in Yusuf Tunca's work include Inflammasome and immune disorders (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Prenatal Screening and Diagnostics (4 papers). Yusuf Tunca is often cited by papers focused on Inflammasome and immune disorders (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Prenatal Screening and Diagnostics (4 papers). Yusuf Tunca collaborates with scholars based in Türkiye, Serbia and United States. Yusuf Tunca's co-authors include Avirachan T. Tharapel, R. Sid Wilroy, Paula R. Martens, Stephen S. Wachtel, Davut Gül, Seza Özen, Erkan Demirkaya, Faysal Gök, Necat İmirzalıoğlu and Hakan Erdem and has published in prestigious journals such as American Journal of Medical Genetics, Prenatal Diagnosis and Clinical Rheumatology.

In The Last Decade

Yusuf Tunca

26 papers receiving 258 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yusuf Tunca Türkiye 11 154 90 67 50 41 30 270
Jacqueline Araújo Brazil 10 123 0.8× 130 1.4× 100 1.5× 23 0.5× 16 0.4× 19 305
İbrahim Keser Türkiye 11 108 0.7× 56 0.6× 36 0.5× 26 0.5× 35 0.9× 32 291
Bettina Hansen Denmark 10 99 0.6× 72 0.8× 115 1.7× 43 0.9× 11 0.3× 15 342
Christian Vasseur France 4 459 3.0× 65 0.7× 268 4.0× 61 1.2× 25 0.6× 6 553
Hotaka Kamasaki Japan 9 162 1.1× 59 0.7× 87 1.3× 25 0.5× 10 0.2× 24 282
Keiichi Hara Japan 13 146 0.9× 56 0.6× 48 0.7× 41 0.8× 39 1.0× 37 349
Francesco Favero Italy 7 80 0.5× 43 0.5× 41 0.6× 77 1.5× 25 0.6× 14 228
Malini Sharma United Kingdom 11 110 0.7× 20 0.2× 26 0.4× 13 0.3× 65 1.6× 27 468
L. Harman United States 6 188 1.2× 184 2.0× 26 0.4× 13 0.3× 50 1.2× 10 309
Rajshekhar Chatterjee India 8 112 0.7× 31 0.3× 73 1.1× 8 0.2× 27 0.7× 11 285

Countries citing papers authored by Yusuf Tunca

Since Specialization
Citations

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

Fields of papers citing papers by Yusuf Tunca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yusuf Tunca

This figure shows the co-authorship network connecting the top 25 collaborators of Yusuf Tunca. A scholar is included among the top collaborators of Yusuf Tunca 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 Yusuf Tunca. Yusuf Tunca 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.
Sarı, İ̇smail, İsmail Şimşek, Yusuf Tunca, et al.. (2015). Is there a relationship between gouty arthritis and Mediterranean fever gene mutations?. Revista Brasileira de Reumatologia (English Edition). 55(4). 325–329. 5 indexed citations
2.
Gül, Hanefi Cem, et al.. (2014). Investigation of the Association Between Paraoxonase-1 Gene Polymorphisms and Response to Therapy in Chronic Hepatitis C Patients. Mikrobiyoloji Bulteni. 48(4). 596–605. 2 indexed citations
3.
Sarı, İ̇smail, İsmail Şimşek, Yusuf Tunca, et al.. (2014). Existe uma relação entre a artrite gotosa e as mutações genéticas da febre familiar do Mediterrâneo?. Revista Brasileira de Reumatologia. 55(4). 325–329. 4 indexed citations
4.
Çınar, Muhammet, Sedat Yılmaz, İsmail Şimşek, et al.. (2013). A polymorphism in ERAP1 is associated with susceptibility to ankylosing spondylitis in a Turkish population. Rheumatology International. 33(11). 2851–2858. 18 indexed citations
5.
Karaşahin, Kazım Emre, et al.. (2013). Travelling after amniocentesis: Answer to a frequent question. Journal of Obstetrics and Gynaecology. 33(4). 343–345.
6.
Tunca, Yusuf, Altuğ Koç, Halide Kaya, et al.. (2013). Prenatal Diagnosis of an Autosomal Translocation with Regular Trisomy 21. Fetal and Pediatric Pathology. 32(3). 210–212.
7.
Arslan, Mutluay, Uluç Yiş, Sebahattin Vurucu, et al.. (2011). Ring chromosome 21 in the differential diagnosis of waddling gait. Brain and Development. 34(9). 792–795. 3 indexed citations
8.
Çelik, Serkan, Alev Akyol Erikçi, Yusuf Tunca, et al.. (2010). The rate of MEFV gene mutations in hematolymphoid neoplasms. International Journal of Immunogenetics. 37(5). 387–391. 11 indexed citations
9.
Öktenli, Çağatay, Özkan Sayan, Serkan Çelik, et al.. (2010). High frequency of MEFV gene mutations in patients with myeloid neoplasm. International Journal of Hematology. 91(5). 758–761. 6 indexed citations
10.
Müngen, Ercüment, Özgür Dündar, Murat Muhçu, Aptullah Haholu, & Yusuf Tunca. (2008). Placental mesenchymal dysplasia associated with trisomy 13: Sonographic findings. Journal of Clinical Ultrasound. 36(7). 454–456. 18 indexed citations
11.
Demirkaya, Erkan, Yusuf Tunca, Faysal Gök, Seza Özen, & Davut Gül. (2007). A very frequent mutation and remarkable association of R761H with M694V mutations in Turkish familial Mediterranean fever patients. Clinical Rheumatology. 27(6). 729–732. 31 indexed citations
12.
Solmazgül, Emrullah, et al.. (2006). Çorum İli ve Çevresinde Ailesel Akdeniz Ateşi Artriti Olarak Farklı Bir Fenotip mi Var. Turkiye Klinikleri Tip Bilimleri Dergisi. 26(1). 20–23.
13.
Tunca, Yusuf, Sebahattin Vurucu, Jasmine Parma, et al.. (2006). Prenatal diagnosis of primary microcephaly in two consanguineous families by confrontation of morphometry with DNA data. Prenatal Diagnosis. 26(5). 449–453. 6 indexed citations
14.
Tunca, Yusuf, et al.. (2003). New heritable fragile site at 15q13 in both members of a nonconsanguineous couple. American Journal of Medical Genetics Part A. 118A(3). 290–292. 8 indexed citations
15.
Wachtel, Stephen S., et al.. (2001). Deletion of RBM and DAZ in azoospermia: Evaluation by PRINS. American Journal of Medical Genetics. 107(2). 105–108. 16 indexed citations
16.
Tunca, Yusuf, et al.. (2000). Chromosomal Localization of Single Copy Genes SRY and SOX3 by Primed In Situ Labeling (PRINS). PubMed. 5(2). 71–74. 15 indexed citations
17.
Tunca, Yusuf, et al.. (2000). Hypomelanosis of Ito and a ‘mirror image’ whole chromosome duplication resulting in trisomy 14 mosaicism. Annales de Génétique. 43(1). 39–43. 17 indexed citations
18.
Wachtel, Stephen S., et al.. (2000). Localization of SRY by primed in situ labeling in XX and XY sex reversal. American Journal of Medical Genetics. 95(1). 71–74. 27 indexed citations
19.
Güran, Şefık, et al.. (1999). Hereditary TP53 Codon 292 and Somatic P16INK4A Codon 94 Mutations in a Li-Fraumeni Syndrome Family. Cancer Genetics and Cytogenetics. 113(2). 145–151. 11 indexed citations
20.
Oğur, Gönül, Samim Özen, Necat İmirzalıoğlu, et al.. (1997). Application of the ‘Apt test’ in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies. Prenatal Diagnosis. 17(9). 879–882. 7 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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