Ercan Mıhçı

1.5k total citations
65 papers, 759 citations indexed

About

Ercan Mıhçı is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Ercan Mıhçı has authored 65 papers receiving a total of 759 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 28 papers in Molecular Biology and 10 papers in Surgery. Recurrent topics in Ercan Mıhçı's work include Genomic variations and chromosomal abnormalities (15 papers), Craniofacial Disorders and Treatments (9 papers) and Cleft Lip and Palate Research (8 papers). Ercan Mıhçı is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Craniofacial Disorders and Treatments (9 papers) and Cleft Lip and Palate Research (8 papers). Ercan Mıhçı collaborates with scholars based in Türkiye, United States and Italy. Ercan Mıhçı's co-authors include Banu Nur, Tomris Özben, Şenay Haspolat, Mesut Çoşkun, Olcay Yeğin, Saadet Gümüşlü, Özgül M. Alper, Güven Lüleci, İbrahim Keser and Elanur Yılmaz and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Journal of Bone and Mineral Research.

In The Last Decade

Ercan Mıhçı

59 papers receiving 714 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ercan Mıhçı Türkiye 13 383 264 122 92 92 65 759
Gözde Yeşil Türkiye 15 290 0.8× 205 0.8× 54 0.4× 88 1.0× 59 0.6× 78 679
Marion Gérard France 14 436 1.1× 386 1.5× 107 0.9× 77 0.8× 36 0.4× 29 837
Katie Morrison United Kingdom 15 273 0.7× 248 0.9× 124 1.0× 96 1.0× 71 0.8× 29 845
Rita Genesio Italy 19 496 1.3× 463 1.8× 92 0.8× 204 2.2× 37 0.4× 52 998
Mustafa Solak Türkiye 16 325 0.8× 102 0.4× 154 1.3× 79 0.9× 54 0.6× 54 708
Almuth Caliebe Germany 23 655 1.7× 678 2.6× 97 0.8× 324 3.5× 96 1.0× 66 1.4k
Tomoyasu Higashimoto United States 14 425 1.1× 272 1.0× 27 0.2× 52 0.6× 84 0.9× 25 697
Siddharth Banka United Kingdom 18 339 0.9× 480 1.8× 104 0.9× 69 0.8× 55 0.6× 55 991
Bertrand Calippe France 15 325 0.8× 181 0.7× 53 0.4× 23 0.3× 94 1.0× 20 1.2k
Eveliina Jakkula Finland 10 230 0.6× 283 1.1× 59 0.5× 40 0.4× 32 0.3× 20 610

Countries citing papers authored by Ercan Mıhçı

Since Specialization
Citations

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

Fields of papers citing papers by Ercan Mıhçı

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ercan Mıhçı

This figure shows the co-authorship network connecting the top 25 collaborators of Ercan Mıhçı. A scholar is included among the top collaborators of Ercan Mıhçı 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 Ercan Mıhçı. Ercan Mıhçı 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.
Güneş, Nilay, et al.. (2023). Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas. Turkish Archives of Pediatrics. 58(4). 376–381. 1 indexed citations
3.
Uysal, Hilmi, et al.. (2022). Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA. Gene. 823. 146322–146322. 2 indexed citations
4.
Yılmaz, Elanur, Banu Nur, Ercan Mıhçı, et al.. (2022). Novel Gene Variants Associated with Primary Ciliary Dyskinesia. The Indian Journal of Pediatrics. 89(7). 682–691. 5 indexed citations
5.
Cammarata‐Scalisi, Francisco, et al.. (2019). Hallazgos clínicos y genéticos de dos casos con síndrome de Apert. Boletín Médico del Hospital Infantil de México. 76(1). 44–48. 4 indexed citations
6.
Yılmaz, Elanur, et al.. (2019). Recent Advances in Craniosynostosis. Pediatric Neurology. 99. 7–15. 27 indexed citations
7.
Mıhçı, Ercan, et al.. (2018). Early postoperative follow-up after craniosynostosis surgery. DergiPark (Istanbul University).
8.
Nur, Banu, et al.. (2013). Possible autosomal recessive inheritance in an infant with acrofacial dysostosis similar to nager syndrome. American Journal of Medical Genetics Part A. 161(9). 2311–2315. 10 indexed citations
9.
Çetin, Zafer, et al.. (2012). A 5q12.1–5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement. Gene. 516(1). 176–180. 9 indexed citations
10.
Simon, Marleen, Belinda Campos‐Xavier, Eugênia Ribeiro Valadares, et al.. (2012). Severe neurologic manifestations from cervical spine instability in spondylo‐megaepiphyseal‐metaphyseal dysplasia. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 160C(3). 230–237. 7 indexed citations
11.
Kardelen, Fırat, et al.. (2011). Prenatal Diagnosis of Mobile Flap-Like Tissue on the Ventricular Septal Defect in a Newborn with Trisomy 18. Echocardiography. 28(9). E191–E193.
12.
Çetin, Zafer, et al.. (2011). Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12. American Journal of Medical Genetics Part A. 155(2). 349–352. 17 indexed citations
13.
Mıhçı, Ercan, Erdal Eren, Fırat Kardelen, et al.. (2010). Evaluation of congenital heart diseases and thyroid abnormalities in children with Down syndrome. Anadolu Kardiyoloji Dergisi/The Anatolian Journal of Cardiology. 10(5). 440–445. 18 indexed citations
14.
Hellemans, Jan, Marleen Simon, Annelies Dheedene, et al.. (2009). Homozygous Inactivating Mutations in the NKX3-2 Gene Result in Spondylo-Megaepiphyseal-Metaphyseal Dysplasia. The American Journal of Human Genetics. 85(6). 916–922. 28 indexed citations
15.
Mıhçı, Ercan, et al.. (2009). Neutrophil oxidative metabolism in Down syndrome patients with congenital heart defects. Environmental and Molecular Mutagenesis. 51(1). 57–63. 12 indexed citations
16.
Mendilcioğlu, İnanç, Ercan Mıhçı, Elif Peştereli, & Mehmet Şimşek. (2009). Prenatal diagnosis of Gollop–Wolfgang complex (tibial agenesis and femoral bifurcation). Prenatal Diagnosis. 29(2). 182–186. 4 indexed citations
17.
Kamath, Binita M., Brian Thiel, Xiaowu Gai, et al.. (2008). SNP array mapping of chromosome 20p deletions: Genotypes, phenotypes, and copy number variation. Human Mutation. 30(3). 371–378. 46 indexed citations
18.
Onur, Mehmet Ruhi, Utku Şenol, Ercan Mıhçı, & Ersin Lüleci. (2008). Tigroid pattern on magnetic resonance imaging in Lowe syndrome. Journal of Clinical Neuroscience. 16(1). 112–114. 10 indexed citations
19.
Mıhçı, Ercan, et al.. (2005). Konjenital Anomalilere Güncel Yaklaşım. 1(2). 48–55. 1 indexed citations
20.
Aslan, Adnan, et al.. (2005). Currarino syndrome associated with penoscrotal inversion and perineal fissure. Pediatric Surgery International. 21(9). 733–735. 8 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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