E Tunçbilek

1.1k total citations
52 papers, 814 citations indexed

About

E Tunçbilek is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, E Tunçbilek has authored 52 papers receiving a total of 814 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Pediatrics, Perinatology and Child Health and 13 papers in Surgery. Recurrent topics in E Tunçbilek's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Congenital Diaphragmatic Hernia Studies (4 papers). E Tunçbilek is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Congenital Diaphragmatic Hernia Studies (4 papers). E Tunçbilek collaborates with scholars based in Türkiye, United States and Germany. E Tunçbilek's co-authors include İsmet Koç, Mehmet Alikaşifoğlu, Koray Boduroğlu, Müjgan Alikaşifoğlu, Ayşı̇n Bakkaloğlu, Dilek Aktaş, Seza Özen, Nesrin Beşbaş, Kateřina Jarošová and Dana Němcová and has published in prestigious journals such as The American Journal of Gastroenterology, Heart and Journal of Periodontology.

In The Last Decade

E Tunçbilek

52 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E Tunçbilek Türkiye	15	198	195	175	172	151	52	814
M. Hauge Denmark	16	101 0.5×	232 1.2×	149 0.9×	51 0.3×	161 1.1×	31	827
Rabah M. Shawky Egypt	13	102 0.5×	173 0.9×	184 1.1×	72 0.4×	143 0.9×	66	615
Maria Francesca Messina Italy	21	191 1.0×	285 1.5×	215 1.2×	78 0.5×	125 0.8×	63	1.0k
Piet F. Dijkstra Netherlands	19	456 2.3×	322 1.7×	216 1.2×	225 1.3×	90 0.6×	55	1.1k
Greetje de Jong South Africa	16	185 0.9×	88 0.5×	153 0.9×	70 0.4×	140 0.9×	36	762
Inusha Panigrahi India	17	108 0.5×	254 1.3×	267 1.5×	90 0.5×	153 1.0×	145	1.0k
Norbert Albers Germany	18	145 0.7×	251 1.3×	468 2.7×	147 0.9×	133 0.9×	38	1.1k
Nurçin Saka Türkiye	18	177 0.9×	265 1.4×	307 1.8×	45 0.3×	187 1.2×	63	961
Helen Foster United Kingdom	21	200 1.0×	242 1.2×	532 3.0×	175 1.0×	88 0.6×	54	1.2k
Joel David United Kingdom	21	182 0.9×	90 0.5×	270 1.5×	311 1.8×	70 0.5×	63	1.3k

Countries citing papers authored by E Tunçbilek

Since Specialization

Citations

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

Fields of papers citing papers by E Tunçbilek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E Tunçbilek

This figure shows the co-authorship network connecting the top 25 collaborators of E Tunçbilek. A scholar is included among the top collaborators of E Tunçbilek 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 E Tunçbilek. E Tunçbilek 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

Ütine, Gülen Eda, Yasemin Alanay, Göknur Haliloğlu, et al.. (2011). Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability. Molecular Syndromology. 2(2). 64–71. 7 indexed citations

Aktaş, Dilek, Melis Gültekin, Mehmet Alikaşifoğlu, et al.. (2010). Identification of point mutations and large rearrangements in the BRCA1 gene in 667 Turkish unselected ovarian cancer patients. Gynecologic Oncology. 119(1). 131–135. 13 indexed citations

Tekin, Mustafa, Hatice Akay, Suat Fítöz, et al.. (2008). Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. Clinical Genetics. 73(6). 554–565. 41 indexed citations

Alanay, Yasemin, Fatih Ünal, Güzide Turanlı, et al.. (2007). A multidisciplinary approach to the management of individuals with fragile X syndrome. Journal of Intellectual Disability Research. 51(2). 151–161. 30 indexed citations

Esinler, İbrahim, Dilek Aktaş, Mehmet Alikaşifoğlu, E Tunçbilek, & A. Ayhan. (2006). CYP1A1 gene polymorphism and risk of endometrial hyperplasia and endometrial carcinoma. International Journal of Gynecological Cancer. 16(3). 1407–1411. 13 indexed citations

Tütüncü, Neslihan Başçıl, Tomris Erbaş, Mehmet Alikaşifoğlu, & E Tunçbilek. (2005). Thermolabile methylenetetrahydrofolate reductase enzyme genotype is frequent in type 2 diabetic patients with normal fasting homocysteine levels. Journal of Internal Medicine. 257(5). 446–453. 14 indexed citations

Önderoğlu, Lütfü, et al.. (2003). Prenatal diagnosis of laryngeal atresia. Prenatal Diagnosis. 23(4). 277–280. 18 indexed citations

Yetgin, Sevgi, Murat Tuncer, Mustafa Çetın, et al.. (2003). Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up. Leukemia. 17(2). 328–333. 31 indexed citations

Özen, Seza, Mehmet Alikaşifoğlu, Ayşı̇n Bakkaloğlu, et al.. (2002). Tumour necrosis factor α G→A −238 and G→A −308 polymorphisms in juvenile idiopathic arthritis. Lara D. Veeken. 41(2). 223–227. 68 indexed citations

10.

Tunçbilek, E, Koray Boduroğlu, & Mehmet Alikaşifoğlu. (2000). Results of the Turkish congenital malformation survey.. PubMed. 41(3). 287–97. 22 indexed citations

11.

Boduroğlu, Koray & E Tunçbilek. (1999). Two siblings with Bloom's syndrome exhibit different clinical features: possible effect of sex. The Turkish Journal of Pediatrics. 41(1). 107–111. 5 indexed citations

12.

Koç, Ahmet, R. Öner, C. Öner, et al.. (1999). Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient. PubMed. 41(4). 187–189. 2 indexed citations

13.

Aktaş, Dilek, et al.. (1998). No Evidence for Overexpression of the p53 Protein and Mutations in Exons 4–9 of the p53 Gene in a Large Family With Adenomatous Polyposis. The American Journal of Gastroenterology. 93(9). 1524–1526. 2 indexed citations

14.

Olcay, Lale, Fatma Gümrük, Koray Boduroğlu, Turgay Coşkun, & E Tunçbilek. (1998). Anaemia and thrombocytopenia due to haemophagocytosis in a 7‐month‐old boy with galactosialidosis. Journal of Inherited Metabolic Disease. 21(6). 679–680. 13 indexed citations

15.

Cengiz, Turgut Bora, et al.. (1997). Chlamydial infections and male infertility. International Urology and Nephrology. 29(6). 687–693. 36 indexed citations

16.

Tunçbilek, E & İsmet Koç. (1994). Consanguineous marriage in Turkey and its impact on fertility and mortality. Annals of Human Genetics. 58(4). 321–329. 100 indexed citations

17.

Çataltepe, Sule & E Tunçbilek. (1992). A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity. European Journal of Pediatrics. 151(4). 288–290. 13 indexed citations

18.

Kaya, İsa, et al.. (1988). Achondrogenesis type II. Pediatric Radiology. 19(1). 53–53. 2 indexed citations

19.

Tunçbilek, E, et al.. (1978). Are sex chromosone abnormalities a factor in speech delay?. Archives of Disease in Childhood. 53(10). 831–831. 3 indexed citations

20.

Altay, Çiğdem, Burhan Say, & E Tunçbilek. (1974). Frequency of Red Cell Adenosine Deaminase and 6-Phosphogluconate Dehydrogenase in a Sample of the Turkish Population. Human Heredity. 24(3). 306–308. 14 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.

Explore authors with similar magnitude of impact