Dilek Aktaş

617 total citations
14 papers, 106 citations indexed

About

Dilek Aktaş is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Dilek Aktaş has authored 14 papers receiving a total of 106 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Dilek Aktaş's work include Acute Myeloid Leukemia Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Lysosomal Storage Disorders Research (2 papers). Dilek Aktaş is often cited by papers focused on Acute Myeloid Leukemia Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Lysosomal Storage Disorders Research (2 papers). Dilek Aktaş collaborates with scholars based in Türkiye and Germany. Dilek Aktaş's co-authors include Ergül Tunçbılek, Mehmet Alikaşifoğlu, Koray Boduroğlu, Yasemin Alanay, Lale Olcay, Murat Tuncer, İdil Yenicesu, Mualla Çetin, Ahmet Koç and Gönül Hiçsönmez and has published in prestigious journals such as SHILAP Revista de lepidopterología, Developmental Medicine & Child Neurology and American Journal of Hematology.

In The Last Decade

Dilek Aktaş

14 papers receiving 92 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dilek Aktaş Türkiye 6 38 29 26 25 23 14 106
Yasufumi Ohtsuka Japan 9 68 1.8× 78 2.7× 25 1.0× 10 0.4× 12 0.5× 20 228
Oğuz Çilingir Türkiye 8 47 1.2× 87 3.0× 12 0.5× 14 0.6× 12 0.5× 39 166
Guillaume Jedraszak France 7 62 1.6× 53 1.8× 18 0.7× 8 0.3× 12 0.5× 26 147
Evelin Mihailov Estonia 7 30 0.8× 37 1.3× 6 0.2× 12 0.5× 16 0.7× 10 114
Figen Celep Türkiye 9 80 2.1× 47 1.6× 4 0.2× 35 1.4× 18 0.8× 17 194
Ruth Armstrong United Kingdom 6 27 0.7× 25 0.9× 7 0.3× 14 0.6× 6 0.3× 16 108
Ernst Mayerhofer United States 6 12 0.3× 25 0.9× 17 0.7× 15 0.6× 9 0.4× 20 103
Susan Maillard United Kingdom 5 9 0.2× 12 0.4× 14 0.5× 14 0.6× 39 1.7× 6 115
Mohammadreza Dehghani Iran 7 41 1.1× 75 2.6× 3 0.1× 17 0.7× 5 0.2× 24 133
Sandhya Parkash Canada 4 35 0.9× 23 0.8× 4 0.2× 7 0.3× 27 1.2× 6 75

Countries citing papers authored by Dilek Aktaş

Since Specialization
Citations

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

Fields of papers citing papers by Dilek Aktaş

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dilek Aktaş

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

All Works

14 of 14 papers shown
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Haliloğlu, Göknur, et al.. (2016). Congenital myasthenic syndrome due to COLQ mutations: Clues for diagnosis. Neuromuscular Disorders. 26. S112–S112. 1 indexed citations
4.
KILIÇ, Esra KAYA, İlker Ertuğrul, Sema Özer, et al.. (2016). Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene.. SHILAP Revista de lepidopterología. 56(5). 542–5. 3 indexed citations
5.
Demir, Hacı Ahmet, et al.. (2011). WAGR Syndrome With Tetralogy of Fallot and Hydrocephalus. Journal of Pediatric Hematology/Oncology. 33(4). e174–e175. 4 indexed citations
6.
Ütine, Gülen Eda, Hasan Tolga Çelik, Yasemin Alanay, et al.. (2009). Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients. The Turkish Journal of Pediatrics. 51(3). 199–206. 5 indexed citations
7.
Ütine, Gülen Eda, et al.. (2008). Unilateral Peters' anomaly in an infant with 22q11.2 deletion syndrome. Clinical Dysmorphology. 17(4). 289–290. 5 indexed citations
8.
Balcı, Sevim, Aysun Ünal, Dilek Aktaş, et al.. (2007). Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1–11.2;p13.3). Developmental Medicine & Child Neurology. 49(3). 219–224. 19 indexed citations
9.
Aktaş, Dilek, et al.. (2007). Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.. PubMed. 18(2). 171–7. 5 indexed citations
10.
Olcay, Lale, Sevgi Yetgin, Esra Erdemlı, et al.. (2006). Congenital dysgranulopoietic neutropenia. Pediatric Blood & Cancer. 50(1). 115–119. 5 indexed citations
11.
Boduroğlu, Koray, Yasemin Alanay, Mehmet Alikaşifoğlu, Dilek Aktaş, & Ergül Tunçbılek. (2006). Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.. PubMed. 47(4). 327–33. 22 indexed citations
12.
Hiçsönmez, Gönül, Mualla Çetin, İdil Yenicesu, et al.. (2001). Evaluation of Children with Myelodysplastic Syndrome: Importance of Extramedullary Disease as a Presenting Symptom. Leukemia & lymphoma. 42(4). 665–674. 27 indexed citations
13.
Aktaş, Dilek, et al.. (1999). Loss of maternal allele in a child with myelodysplastic syndrome and monosomy 7. American Journal of Hematology. 62(1). 49–51. 3 indexed citations
14.
Topaloğlu, Rezan, Dilek Aktaş, Ayşı̇n Bakkaloğlu, et al.. (1998). Diploid-triploid and tetraploid mosaicism in a child with cryptogenic cirrhosis and membranous glomerulonephritis: a causal relationship or coincidental association?. PubMed. 40(1). 139–43. 1 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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