Eda Ütine

516 total citations
24 papers, 218 citations indexed

About

Eda Ütine is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Eda Ütine has authored 24 papers receiving a total of 218 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Eda Ütine's work include Genomic variations and chromosomal abnormalities (4 papers), Congenital Diaphragmatic Hernia Studies (2 papers) and Connective tissue disorders research (2 papers). Eda Ütine is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Congenital Diaphragmatic Hernia Studies (2 papers) and Connective tissue disorders research (2 papers). Eda Ütine collaborates with scholars based in Türkiye, United Kingdom and United States. Eda Ütine's co-authors include Yasemin Alanay, Koray Boduroğlu, Pelin Özlem Şimşek‐Kiper, Dilek Aktaş, Ergül Tunçbılek, Ekim Z. Taşkıran, Beril Talim, Esra KAYA KILIÇ, Melda Çaǧlar and Lütfü Önderoğlu and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Journal of Medical Genetics.

In The Last Decade

Eda Ütine

22 papers receiving 213 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eda Ütine Türkiye 9 99 96 28 23 22 24 218
Helle Lybæk Norway 10 162 1.6× 114 1.2× 32 1.1× 23 1.0× 19 0.9× 15 282
Andrew Wang United States 6 93 0.9× 146 1.5× 33 1.2× 29 1.3× 17 0.8× 10 328
Karthik Muthusamy India 10 42 0.4× 118 1.2× 25 0.9× 14 0.6× 15 0.7× 43 268
Birutė Burnytė Lithuania 7 70 0.7× 103 1.1× 27 1.0× 9 0.4× 18 0.8× 28 194
Irén Haltrich Hungary 9 93 0.9× 103 1.1× 9 0.3× 11 0.5× 15 0.7× 33 239
Yukiko Kuroda Japan 11 178 1.8× 127 1.3× 17 0.6× 14 0.6× 27 1.2× 40 271
Giacomo Maria Bacci Italy 10 36 0.4× 148 1.5× 28 1.0× 21 0.9× 28 1.3× 40 289
Mathilde Nizon France 13 153 1.5× 239 2.5× 22 0.8× 20 0.9× 28 1.3× 26 387
Dhanya Lakshmi Narayanan India 10 88 0.9× 135 1.4× 13 0.5× 7 0.3× 19 0.9× 42 261
Juliette Piard France 10 121 1.2× 151 1.6× 8 0.3× 10 0.4× 15 0.7× 24 253

Countries citing papers authored by Eda Ütine

Since Specialization
Citations

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

Fields of papers citing papers by Eda Ütine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eda Ütine

This figure shows the co-authorship network connecting the top 25 collaborators of Eda Ütine. A scholar is included among the top collaborators of Eda Ütine 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 Eda Ütine. Eda Ütine 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.
Orhan, Dıclehan, Şafak Güçer, Pelin Özlem Şimşek‐Kiper, et al.. (2024). AP-1-dependent fibrosis: Exploring its potential role in the pathogenesis of placental transmogrification of the lung (PTL) via tissue-level transcriptome analysis. Pathology - Research and Practice. 258. 155334–155334.
2.
Ütine, Eda, et al.. (2024). Allele-specific antisense oligonucleotides for the treatment of BEST1-related dominantly inherited retinal diseases: An in vitro model. Experimental Eye Research. 241. 109833–109833. 1 indexed citations
3.
Taşkıran, Ekim Z., et al.. (2022). Recurrent squamous cell carcinoma and a novel mutation in a patient with xeroderma pigmentosum: a case report. Journal of Medical Case Reports. 16(1). 306–306. 4 indexed citations
4.
Şimşek‐Kiper, Pelin Özlem, Can Koşukçu, Ekim Z. Taşkıran, et al.. (2022). Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review. Pediatric Gastroenterology Hepatology & Nutrition. 25(6). 441–441. 1 indexed citations
5.
Taşkıran, Ekim Z., Pelin Özlem Şimşek‐Kiper, Eda Ütine, et al.. (2021). Spondyloepimetaphyseal dysplasia EXTL3‐deficient type: Long‐term follow‐up and review of the literature. American Journal of Medical Genetics Part A. 185(10). 3104–3110. 5 indexed citations
6.
Şimşek‐Kiper, Pelin Özlem, Can Koşukçu, Ekim Z. Taşkıran, et al.. (2021). Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features. American Journal of Medical Genetics Part A. 185(6). 1888–1896. 12 indexed citations
7.
Ütine, Eda, et al.. (2021). Refractory Temporal Lobe Epilepsy in Patients with Mosaic Turner Syndrome. SHILAP Revista de lepidopterología. 38(3). 194–198.
8.
Atık, Tahir, Şükran Darcan, Samim Özen, et al.. (2020). A rare cause of syndromic short stature: 3M syndrome in three families. American Journal of Medical Genetics Part A. 185(2). 461–468. 7 indexed citations
9.
Takçı, Şahin, Heike Kotarsky, Onur Çil, et al.. (2016). A Turkish BCS1L mutation causes GRACILE-like disorder. The Turkish Journal of Pediatrics. 58(6). 658–661. 6 indexed citations
10.
Özsürekçi, Yasemin, et al.. (2014). Partial distal aphalangia, duplication of metatarsal IV, microcephaly, and borderline intelligence. Clinical Dysmorphology. 24(1). 29–33. 2 indexed citations
11.
12.
Tarlan, Berçin, Hayyam Kıratlı, Esra KAYA KILIÇ, Eda Ütine, & Koray Boduroğlu. (2013). A Case of 22q11.2 Deletion Syndrome with Right Microphthalmia and Left Corneal Staphyloma. Ophthalmic Genetics. 35(4). 248–251. 5 indexed citations
13.
Alanay, Yasemin, Bekir Ergüner, Eda Ütine, et al.. (2013). TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia. American Journal of Medical Genetics Part A. 164(2). 291–304. 23 indexed citations
14.
Alanay, Yasemin, et al.. (2012). Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 gene.. SHILAP Revista de lepidopterología. 54(2). 198–202. 8 indexed citations
15.
KILIÇ, Esra KAYA, Eda Ütine, Şule Ünal, et al.. (2012). Medical management of moyamoya disease and recurrent stroke in an infant with Majewski osteodysplastic primordial dwarfism type II (MOPD II). European Journal of Pediatrics. 171(10). 1567–1571. 12 indexed citations
16.
Ki̇per, Nural, Filiz Özbas‐Gerçeker, Eda Ütine, et al.. (2010). TAP1 and TAP2 gene polymorphisms in childhood cystic echinococcosis. Parasitology International. 59(2). 283–285. 10 indexed citations
17.
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
18.
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
19.
Cilliers, Deirdre, Yasemin Alanay, Koray Boduroğlu, et al.. (2007). Cerebro-facio-thoracic dysplasia: expanding the phenotype. Clinical Dysmorphology. 16(2). 121–125. 7 indexed citations
20.
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

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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