Selma Demır

699 total citations
61 papers, 431 citations indexed

About

Selma Demır is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Selma Demır has authored 61 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 22 papers in Genetics and 12 papers in Surgery. Recurrent topics in Selma Demır's work include Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (6 papers) and Genomics and Rare Diseases (5 papers). Selma Demır is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (6 papers) and Genomics and Rare Diseases (5 papers). Selma Demır collaborates with scholars based in Türkiye, United States and Cyprus. Selma Demır's co-authors include Hakan Gürkan, Aydanur Ekici, Ercan Kurtipek, Ahmet Akın, Mehmet Ekici, Mazyar Javidroozi, Aryeh Shander, Emine İkbal Atlı, Hilmi Tozkır and G. Hempelmann and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and CHEST Journal.

In The Last Decade

Selma Demır

48 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Selma Demır Türkiye 9 94 78 73 71 62 61 431
Dean English Canada 16 179 1.9× 204 2.6× 7 0.1× 57 0.8× 52 0.8× 19 906
Manelle Ramadan United States 11 43 0.5× 73 0.9× 14 0.2× 22 0.3× 16 0.3× 19 331
Joji Miyawaki Japan 12 25 0.3× 298 3.8× 9 0.1× 38 0.5× 34 0.5× 22 557
Teruki Kidani Japan 12 67 0.7× 230 2.9× 6 0.1× 38 0.5× 42 0.7× 38 598
T. Nelson United States 11 101 1.1× 33 0.4× 8 0.1× 28 0.4× 56 0.9× 15 496
Soetkin Van kerckhoven Belgium 11 184 2.0× 90 1.2× 6 0.1× 17 0.2× 15 0.2× 14 588
Jiahao Zhu China 15 143 1.5× 39 0.5× 6 0.1× 18 0.3× 76 1.2× 55 595
Shannon Bainbridge Canada 24 344 3.7× 84 1.1× 4 0.1× 84 1.2× 31 0.5× 57 1.9k
Sun Haeng Kim South Korea 17 121 1.3× 33 0.4× 9 0.1× 8 0.1× 77 1.2× 37 873

Countries citing papers authored by Selma Demır

Since Specialization
Citations

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

Fields of papers citing papers by Selma Demır

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Selma Demır

This figure shows the co-authorship network connecting the top 25 collaborators of Selma Demır. A scholar is included among the top collaborators of Selma Demır 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 Selma Demır. Selma Demır 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.
Demır, Selma, et al.. (2024). Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss. The Journal of International Advanced Otology. 20(4). 312–324.
2.
Atlı, Emine İkbal, et al.. (2024). Next-Generation Sequencing Infertility Panel in Turkey: First Results. SHILAP Revista de lepidopterología. 27(2). 49–57. 1 indexed citations
3.
4.
Demır, Selma, et al.. (2023). The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method. SHILAP Revista de lepidopterología. 10(2). 117–122.
5.
Atlı, Emine İkbal, et al.. (2023). Y chromosome polymorphism in Turkish patients with reproductive problems: a genetic centre experience. The European Research Journal. 9(4). 725–729.
6.
Gürkan, Hakan, et al.. (2022). Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method. SHILAP Revista de lepidopterología. 9(3). 200–207. 1 indexed citations
7.
8.
Atlı, Emine İkbal, et al.. (2022). Prenatal Sitogenetik Anormallikler ve Ultrasonografik olarak Saptanan Fetal Anomalilerin Korelasyonu. OSMANGAZİ JOURNAL OF MEDICINE.
9.
Toksoy, Güven, İbrahim Kalelioğlu, Selma Demır, et al.. (2021). NOONAN SENDROMU’NUN PRENATAL TANISINDA PTPN11 GEN ANALİZLERİNİN ETKİNLİĞİ. SHILAP Revista de lepidopterología. 84(1). 34–39. 1 indexed citations
10.
Demır, Selma, et al.. (2021). RETROSPECTIVE ANALYSIS OF ALPHA GLOBIN COPY NUMBER VARIATIONS DETERMINED BY MLPA IN THE TRAKYA REGION. SHILAP Revista de lepidopterología. 84(3). 348–353. 1 indexed citations
11.
Gürkan, Hakan, et al.. (2021). The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region. Journal of Clinical Research in Pediatric Endocrinology. 13(3). 320–331. 7 indexed citations
12.
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
13.
Görker, İşık, Selma Demır, Emine İkbal Atlı, et al.. (2021). Investigation of the Relationship between Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2 and GABRA4 Genes. Nöro Psikiyatri Arşivi. 58(3). 171–175.
14.
Atlı, Emine İkbal, et al.. (2020). Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma. SHILAP Revista de lepidopterología. 23(2). 59–64. 3 indexed citations
15.
Atlı, Emine İkbal, et al.. (2020). THE IMPORTANCE OF TARGETED NEXT-GENERATION SEQUENCING USAGE IN CYTOGENETICALLY NORMAL MYELOID MALIGNANCIES. Mediterranean Journal of Hematology and Infectious Diseases. 13(1). e2021013–e2021013. 5 indexed citations
16.
Arslan, Selçuk, Hakan Gürkan, Selma Demır, et al.. (2017). Novel EYA1 variants causing Branchio-oto-renal syndrome. International Journal of Pediatric Otorhinolaryngology. 98. 59–63. 15 indexed citations
17.
Atlı, Emine İkbal, et al.. (2016). Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both Fetuses. Fetal and Pediatric Pathology. 35(5). 339–343. 3 indexed citations
18.
Shander, Aryeh, et al.. (2014). An update on mortality and morbidity in patients with very low postoperative hemoglobin levels who decline blood transfusion (CME). Transfusion. 54(10pt2). 2688–2695. 95 indexed citations
19.
Demır, Selma, et al.. (2009). The Analysis of the Relationship Between A1298C and C677T Polymorphisms of the MTHFR Gene with Prostate Cancer in Eskisehir Population. Genetic Testing and Molecular Biomarkers. 13(5). 641–645. 22 indexed citations
20.
Çilingir, Oğuz, et al.. (2006). A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda. British Journal of Dermatology. 155(2). 467–469. 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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