Ayça Aykut

939 total citations
81 papers, 553 citations indexed

About

Ayça Aykut is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Ayça Aykut has authored 81 papers receiving a total of 553 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 30 papers in Molecular Biology and 17 papers in Immunology. Recurrent topics in Ayça Aykut's work include Prenatal Screening and Diagnostics (12 papers), Immunodeficiency and Autoimmune Disorders (11 papers) and Blood disorders and treatments (8 papers). Ayça Aykut is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Immunodeficiency and Autoimmune Disorders (11 papers) and Blood disorders and treatments (8 papers). Ayça Aykut collaborates with scholars based in Türkiye, United States and Germany. Ayça Aykut's co-authors include Ferda Özkınay, Hüseyin Önay, Özgür Çoğulu, Tahir Atık, Asude Durmaz, Burak Durmaz, Emin Karaca, Cumhur Gündüz, Damla Gökşen and Fılız Hazan and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Ayça Aykut

70 papers receiving 538 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ayça Aykut Türkiye 12 247 180 76 71 71 81 553
Rhonda E. Schnur United States 20 505 2.0× 333 1.9× 44 0.6× 72 1.0× 74 1.0× 52 919
Norma Leonard Canada 14 279 1.1× 103 0.6× 55 0.7× 78 1.1× 68 1.0× 30 520
Denny Schanze Germany 18 393 1.6× 223 1.2× 88 1.2× 101 1.4× 20 0.3× 55 749
Ihtisham Bukhari China 16 350 1.4× 120 0.7× 64 0.8× 62 0.9× 34 0.5× 51 724
Heasoo Koo South Korea 18 316 1.3× 75 0.4× 44 0.6× 90 1.3× 25 0.4× 54 875
Moin Mohamed United Kingdom 19 562 2.3× 209 1.2× 41 0.5× 27 0.4× 33 0.5× 36 1.2k
Navid Almadani Iran 14 352 1.4× 233 1.3× 19 0.3× 56 0.8× 76 1.1× 45 702
Juliette Gimenez Spain 12 286 1.2× 108 0.6× 49 0.6× 36 0.5× 72 1.0× 25 603
Matthew Donne United States 7 438 1.8× 39 0.2× 83 1.1× 51 0.7× 81 1.1× 9 793
Ju Gao China 14 335 1.4× 122 0.7× 141 1.9× 48 0.7× 32 0.5× 67 797

Countries citing papers authored by Ayça Aykut

Since Specialization
Citations

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

Fields of papers citing papers by Ayça Aykut

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ayça Aykut

This figure shows the co-authorship network connecting the top 25 collaborators of Ayça Aykut. A scholar is included among the top collaborators of Ayça Aykut 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 Ayça Aykut. Ayça Aykut 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.
2.
Canda, Ebru, Havva Yazıcı, Ayça Aykut, et al.. (2025). Insights into skeletal involvement in adult Gaucher disease: a single-center experience. Journal of Bone and Mineral Metabolism. 43(2). 166–173. 1 indexed citations
3.
Uçar, Sema Kalkan, Havva Yazıcı, Yasemin Atik Altınok, et al.. (2025). Nutritional management and geno-phenotyping of clinical nutrition in patients with glycogen storage diseases type VI and IX. European Journal of Clinical Nutrition. 79(8). 723–730. 1 indexed citations
4.
5.
Çelmeli, Fatih, et al.. (2024). Inborn Errors of Immunity in Pediatric Intensive Care: Prevalence, Characteristics, and Prognosis. Journal of Clinical Immunology. 45(1). 25–25. 1 indexed citations
6.
Aykut, Ayça, et al.. (2024). P-15 A rare case of Trichorhinophalangeal Syndrome Type I. JCEM Case Reports. 2(Supplement_1). 1 indexed citations
7.
Geyik, Mehmet Faruk, Neslihan Edeer Karaca, Asude Durmaz, et al.. (2023). Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience. Immunologic Research. 72(2). 225–233.
8.
Durmaz, Asude, et al.. (2023). A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment. Journal of Clinical Research in Pediatric Endocrinology. 17(3). 337–344. 2 indexed citations
9.
Durmaz, Burak, Hilmi Bolat, Fuat Akercan, et al.. (2021). 20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey. TURKISH JOURNAL OF MEDICAL SCIENCES. 51(4). 1775–1780. 3 indexed citations
10.
Bağca, Bakiye Göker, Emin Karaca, Asude Durmaz, et al.. (2021). Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain CancerStem Cells. Anti-Cancer Agents in Medicinal Chemistry. 22(2). 378–389. 10 indexed citations
11.
Serdaroğlu, Erkin, et al.. (2020). Partial Treatment with Exchange Transfusion in Neonatal Atypical Hemolytic Uremic Syndrome: Case Report. 5(4). 1 indexed citations
12.
Vardarli, Aslı Teti̇k, Levent Pelit, Ayça Aykut, et al.. (2020). * Concordance in molecular genetic analysis of tumour tissue, plasma, and exhaled breath condensate samples from lung cancer patients. Journal of Breath Research. 14(3). 36001–36001. 9 indexed citations
13.
Gürsoy, Semra, Fılız Hazan, Ayça Aykut, et al.. (2020). Detection of <i>SHOX</i> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature. Journal of Clinical Research in Pediatric Endocrinology. 12(4). 358–365. 9 indexed citations
14.
Aykut, Ayça, et al.. (2017). Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation. Journal of Clinical Research in Pediatric Endocrinology. 10(2). 179–182. 8 indexed citations
15.
Karaca, Emin, Ayça Aykut, Burak Durmaz, et al.. (2017). Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome. Balkan Medical Journal. 35(2). 163–166. 24 indexed citations
16.
Karaca, Irmak, Suzan Güven Yılmaz, Melis Palamar, et al.. (2017). Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome. International Ophthalmology. 39(1). 167–173. 2 indexed citations
17.
Aykut, Ayça, Samim Özen, Damla Gökşen, et al.. (2016). Prevalence of Melanocortin 4 Receptor Mutations in Turkish Obese Children. 86. 1 indexed citations
18.
Yılmaz, Suzan Güven, Melis Palamar, Hüseyin Önay, et al.. (2016). LOXL1 gene analysis in Turkish patients with exfoliation glaucoma. International Ophthalmology. 36(5). 629–635. 10 indexed citations
19.
Atık, Tahir, Hüseyin Önay, Ayça Aykut, et al.. (2015). Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. PLoS ONE. 10(11). e0142154–e0142154. 49 indexed citations
20.
Hazan, Fılız, et al.. (2012). Ventricular septal defect in Crouzon Syndrome: case report.. PubMed. 23(4). 519–22. 2 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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