Ergül Tunçbılek

1.5k total citations
55 papers, 831 citations indexed

About

Ergül Tunçbılek is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Ergül Tunçbılek has authored 55 papers receiving a total of 831 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 13 papers in Molecular Biology and 10 papers in Surgery. Recurrent topics in Ergül Tunçbılek's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Ergül Tunçbılek is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Ergül Tunçbılek collaborates with scholars based in Türkiye, Germany and United States. Ergül Tunçbılek's co-authors include Yasemin Alanay, Dilek Aktaş, Koray Boduroğlu, Mehmet Alikaşifoğlu, Meral Özgüç, Burhan Say, Sinan Sözen, Haluk Özen, K. Yüce and Ali̇ Ayhan and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and American Journal of Kidney Diseases.

In The Last Decade

Ergül Tunçbılek

53 papers receiving 786 citations

Peers

Ergül Tunçbılek

GENET

PPCH

RHEUM

SURGE

S. F. Ahmed United Kingdom

Tahsin Yakut Türkiye

M.P. Sachdeva India

Susumu Kanzaki Japan

Tonia C. Carter United States

M. Hauge Denmark

Isabelle Fajardy France

M J Mahoney United States

Michael Gornish Israel

Alessandra Carnevale Mexico

S. F. Ahmed United Kingdom

Ergül Tunçbılek

460 ×1.7

324 ×1.3

GENET

198 ×1.1

PPCH

120 ×0.9

RHEUM

95 ×0.7

SURGE

Citations per year, relative to Ergül Tunçbılek Ergül Tunçbılek (= 1×) peers S. F. Ahmed

Countries citing papers authored by Ergül Tunçbılek

Since Specialization

Citations

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

Fields of papers citing papers by Ergül Tunçbılek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ergül Tunçbılek

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Aktaş, Dilek, Kristin Mrasek, Anja Weise, et al.. (2010). Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair. Molecular Cytogenetics. 3(1). 10–10. 14 indexed citations

Aktaş, Dilek, Anja Weise, Eda Ütine, et al.. (2009). Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report. Molecular Cytogenetics. 2(1). 14–14. 3 indexed citations

Yalçın, Sıddika Songül, et al.. (2007). A Hypotonic Infant With Tachycardia and Fever of Unknown Origin. Journal of Pediatric Health Care. 21(2). 115–116. 1 indexed citations

Taşkıran, Çağatay, Dilek Aktaş, Mehmet Alikaşifoğlu, et al.. (2006). CYP1A1 gene polymorphism as a risk factor for cervical intraepithelial neoplasia and invasive cervical cancer. Gynecologic Oncology. 101(3). 503–506. 19 indexed citations

Tunçbılek, Ergül & Yasemin Alanay. (2006). Congenital contractural arachnodactyly (Beals syndrome). Orphanet Journal of Rare Diseases. 1(1). 20–20. 40 indexed citations

Alanay, Yasemin, Dilek Aktaş, Eda Ütine, et al.. (2005). Is Dandy-Walker malformation associated with “distal 13q deletion syndrome”? Findings in a fetus supporting previous observations. American Journal of Medical Genetics Part A. 136A(3). 265–268. 28 indexed citations

Aktaş, Dilek, Mehmet Alikaşifoğlu, Nazlı Gönç, Mehmet Emin S̆enocak, & Ergül Tunçbılek. (2005). Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis. European Journal of Medical Genetics. 49(2). 141–149. 8 indexed citations

Ütine, Gülen Eda, Ayfer Alikaşifoğlu, Mehmet Alikaşifoğlu, & Ergül Tunçbılek. (2005). Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogue. European Journal of Medical Genetics. 49(1). 79–82. 2 indexed citations

Aktaş, Dilek, et al.. (2004). CYP1A1 and GSTM1 polymorphic genotypes in patients with prostate cancer in a Turkish population. Cancer Genetics and Cytogenetics. 154(1). 81–85. 38 indexed citations

10.

Aktaş, Dilek, et al.. (2002). CYP1A1 Gene Polymorphism and Risk of Epithelial Ovarian Neoplasm. Gynecologic Oncology. 86(2). 124–128. 44 indexed citations

11.

Aktaş, Dilek, Haluk Özen, Necmettın Atsü, et al.. (2001). Glutathione S-transferase M1 gene polymorphism in bladder cancer patients. Cancer Genetics and Cytogenetics. 125(1). 1–4. 29 indexed citations

12.

Aktaş, Dilek, et al.. (2001). Chromosomal Mosaicism in a Pregnant Woman Treated with Acyclovir for Herpes Simplex Encephalitis. American Journal of Perinatology. 18(4). 179–184. 1 indexed citations

13.

Aktaş, Dilek, Ergül Tunçbılek, Mualla Çetin, & Gönül Hiçsönmez. (2001). Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia. Cancer Genetics and Cytogenetics. 126(2). 166–168. 8 indexed citations

14.

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

15.

Aktaş, Dilek, Ahmet Koç, Koray Boduroğlu, Gönül Hiçsönmez, & Ergül Tunçbılek. (2000). Myelodysplastic Syndrome Associated with Monosomy 7 in a Child with Bloom Syndrome. Cancer Genetics and Cytogenetics. 116(1). 44–46. 22 indexed citations

16.

Tokgözoğlu, S. Lale, Enver Atalar, Necla Özer, et al.. (1999). Effects of Plasma Homocysteine Level and MTHFR Genotype on Presence and Extent of Coronary Artery Disease. Archives of the Turkish Society of Cardiology. 27(9). 598–603. 1 indexed citations

17.

Özen, Seza, U Saatçi, A Bakkaloğlu, et al.. (1999). Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: Importance of ace polymorphism. American Journal of Kidney Diseases. 34(1). 140–145. 51 indexed citations

18.

Alikaşifoğlu, Mehmet, et al.. (1997). Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non‐Fanconi anemia): Hacettepe experience. Clinical Genetics. 51(5). 296–302. 25 indexed citations

19.

Saraçlar, Y, Şule Yiğit, Gönül Adalıoğlu, Ayfer Tuncer, & Ergül Tunçbılek. (1997). Prevalence of Allergic Diseases and Influencing Factors in Primary-School Children in the Ankara Region of Turkey. Journal of Asthma. 34(1). 23–30. 29 indexed citations

20.

Say, Burhan, et al.. (1973). Incidence of Congenital Malformations in a Sample of the Turkish Population. Human Heredity. 23(5). 434–441. 21 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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