Sevilhan Artan

1.1k total citations
84 papers, 760 citations indexed

About

Sevilhan Artan is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sevilhan Artan has authored 84 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 21 papers in Genetics and 12 papers in Genetics. Recurrent topics in Sevilhan Artan's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers) and Chromosomal and Genetic Variations (6 papers). Sevilhan Artan is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers) and Chromosomal and Genetic Variations (6 papers). Sevilhan Artan collaborates with scholars based in Türkiye, United States and Switzerland. Sevilhan Artan's co-authors include Alı Arslantaş, Metin Ant Atasoy, Bekir Sıtkı Şaylı, Oğuz Çilingir, Ramazan Durmaz, Eşref Tel, Ülkü Öner, Murat Vural, Cavit Can and Albert Schinzel and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Gene.

In The Last Decade

Sevilhan Artan

69 papers receiving 733 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sevilhan Artan Türkiye 18 308 187 156 148 106 84 760
Pamela S. Karnes United States 17 430 1.4× 199 1.1× 105 0.7× 138 0.9× 123 1.2× 29 992
Lesa Nelson United States 17 205 0.7× 247 1.3× 127 0.8× 108 0.7× 75 0.7× 31 1.3k
Tony Frisk Sweden 13 349 1.1× 125 0.7× 64 0.4× 131 0.9× 79 0.7× 23 857
Bożenna Dembowska–Bagińska Poland 17 448 1.5× 104 0.6× 239 1.5× 111 0.8× 186 1.8× 68 1.0k
Shlomit Goldman Israel 23 366 1.2× 194 1.0× 56 0.4× 167 1.1× 220 2.1× 53 1.6k
Yi Dai China 17 348 1.1× 142 0.8× 65 0.4× 92 0.6× 40 0.4× 50 958
Christine Pérot France 17 357 1.2× 178 1.0× 175 1.1× 61 0.4× 89 0.8× 31 934
Martin Mynarek Germany 16 197 0.6× 71 0.4× 307 2.0× 168 1.1× 78 0.7× 47 672
Sadao Tokimasa Japan 17 385 1.3× 59 0.3× 101 0.6× 157 1.1× 47 0.4× 39 986
Stacy Mosier United States 9 275 0.9× 95 0.5× 126 0.8× 131 0.9× 258 2.4× 9 747

Countries citing papers authored by Sevilhan Artan

Since Specialization
Citations

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

Fields of papers citing papers by Sevilhan Artan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sevilhan Artan

This figure shows the co-authorship network connecting the top 25 collaborators of Sevilhan Artan. A scholar is included among the top collaborators of Sevilhan Artan 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 Sevilhan Artan. Sevilhan Artan 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.
Artan, Sevilhan, et al.. (2025). Comparison of conventional karyotype analysis and CMA results with ultrasound findings in pregnancies with normal QF-PCR results. Journal of Turkish Society of Obstetric and Gynecology. 22(2). 106–113. 1 indexed citations
2.
Artan, Sevilhan, et al.. (2025). Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies. Scientific Reports. 15(1). 16678–16678.
3.
Artan, Sevilhan, et al.. (2024). Interstitial 3p25.3 deletion syndrome: 13 years’-long follow-up of an affected individual. Clinical Dysmorphology. 33(4). 183–186.
4.
Balcıoğlu, Hüseyin, et al.. (2024). Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions?. TURKISH JOURNAL OF MEDICAL SCIENCES. 54(4). 682–687. 1 indexed citations
5.
Dışıbeyaz, Selçuk, et al.. (2023). Genetic Investigations in Turkish Idiopathic Pancreatitis Patients Show Unique Characteristics. The Turkish Journal of Gastroenterology. 34(12). 1240–1248.
6.
Çilingir, Oğuz, et al.. (2023). KLL Olgularında NOTCH1 Gen Amplifikasyonu. OSMANGAZİ JOURNAL OF MEDICINE. 46(1).
7.
Özben, Serkan, et al.. (2023). A novel mutation in RNF216 gene in a Turkish case with Gordon Holmes syndrome. BMC Medical Genomics. 16(1). 98–98. 2 indexed citations
8.
9.
Teke, Hava Üsküdar, et al.. (2021). A new four-way complex translocation variant involving the t(8;5;21;4)(q21;q13;q22;q31) and the relocalization of AML1/ETO fusion gene. Cancer Genetics. 256-257. 1–4. 2 indexed citations
10.
Özdemir, Zeynep Canan, et al.. (2021). A pediatric BAL case with double Ph chromosomes and trisomy 5. Cancer Genetics. 258-259. 7–9.
11.
Şaylısoy, Suzan, et al.. (2021). NDE1‐related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly. American Journal of Medical Genetics Part A. 188(1). 326–331. 1 indexed citations
12.
Artan, Sevilhan, Bedia Samancı, Başar Bılgıç, et al.. (2021). Frequency of frontotemporal dementia-related gene variants in Turkey. Neurobiology of Aging. 106. 332.e1–332.e11. 3 indexed citations
13.
Gündüz, Eren, et al.. (2021). An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3. Cytogenetic and Genome Research. 161(10-11). 479–487. 3 indexed citations
14.
Çilingir, Oğuz, et al.. (2020). A Turkish patient with novel AHCY variants and presumed diagnosis of S‐adenosylhomocysteine hydrolase deficiency. American Journal of Medical Genetics Part A. 182(4). 740–745. 5 indexed citations
15.
Çilingir, Oğuz, et al.. (2017). Association of functional RAGE gene polymorphisms with Parkinson's disease in a Turkish cohort. Biomedical Research-tokyo. 28(19). 8454–8460. 1 indexed citations
16.
Aslan, Hüseyi̇n, Serdar Erkasap, Ayşegül Özakyol, et al.. (2014). Detection of kinase amplifications in gastric adenocarcinomas. TURKISH JOURNAL OF MEDICAL SCIENCES. 44(3). 461–470. 2 indexed citations
17.
Kurt, Emel, et al.. (2014). Is there a genetic predisposition for Turkish patients with sarcoidosis in the 329-bp region containing the BTNL2 rs2076530 polymorphism?. TURKISH JOURNAL OF MEDICAL SCIENCES. 44(4). 590–594. 2 indexed citations
18.
Arslantaş, Alı, Sevilhan Artan, Ülkü Öner, et al.. (2007). Genomic alterations in low-grade, anaplastic astrocytomas and glioblastomas. Pathology & Oncology Research. 13(1). 39–46. 26 indexed citations
19.
Tanir, H. Mete, et al.. (2005). Programmed cell death (apoptosis) in placentas from normal pregnancy and pregnancy complicated by term (t) and preterm (p) premature rupture of membranes (PROM). Archives of Gynecology and Obstetrics. 273(2). 98–103. 26 indexed citations
20.
Artan, Sevilhan, et al.. (1994). Effects of consanguinity on anthropometric measurements of newborn infants. Clinical Genetics. 45(4). 208–211. 16 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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