Ercan Demir

995 total citations
24 papers, 732 citations indexed

About

Ercan Demir is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Psychiatry and Mental health. According to data from OpenAlex, Ercan Demir has authored 24 papers receiving a total of 732 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Pediatrics, Perinatology and Child Health and 7 papers in Psychiatry and Mental health. Recurrent topics in Ercan Demir's work include Epilepsy research and treatment (7 papers), Metabolism and Genetic Disorders (4 papers) and Hereditary Neurological Disorders (4 papers). Ercan Demir is often cited by papers focused on Epilepsy research and treatment (7 papers), Metabolism and Genetic Disorders (4 papers) and Hereditary Neurological Disorders (4 papers). Ercan Demir collaborates with scholars based in Türkiye, France and Italy. Ercan Demir's co-authors include Haluk Topaloğlu, P. Landrieu, Samir Belal, L Cavalier, Fayçal Hentati, Pascale Bomont, Beyhan Tüysüz, M. Kœnig, Christiane Ben Hamida and Mériem Tazir and has published in prestigious journals such as Nature Genetics, Neurology and The American Journal of Human Genetics.

In The Last Decade

Ercan Demir

23 papers receiving 722 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 Demir Türkiye 11 368 237 212 117 87 24 732
Friederike Kirsch Germany 12 275 0.7× 106 0.4× 149 0.7× 174 1.5× 118 1.4× 13 683
V. Volpini Spain 17 571 1.6× 369 1.6× 167 0.8× 91 0.8× 167 1.9× 33 996
Andrée Robaglia‐Schlupp France 16 399 1.1× 419 1.8× 84 0.4× 97 0.8× 138 1.6× 30 1.0k
Karen Gorse United States 14 353 1.0× 120 0.5× 94 0.4× 57 0.5× 125 1.4× 21 633
Zofia M. Lasiecka United States 11 564 1.5× 287 1.2× 367 1.7× 70 0.6× 53 0.6× 14 968
Wei‐Ming Duan China 17 421 1.1× 276 1.2× 54 0.3× 154 1.3× 122 1.4× 32 871
Dominic B. Fee United States 13 391 1.1× 294 1.2× 51 0.2× 170 1.5× 203 2.3× 23 801
Marı́a José Barallobre Spain 15 575 1.6× 420 1.8× 206 1.0× 65 0.6× 42 0.5× 18 1.2k
Jeroen Vreijling Netherlands 12 527 1.4× 85 0.4× 55 0.3× 54 0.5× 43 0.5× 19 844
Andrea O’Neill United States 17 629 1.7× 289 1.2× 285 1.3× 36 0.3× 29 0.3× 27 969

Countries citing papers authored by Ercan Demir

Since Specialization
Citations

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

Fields of papers citing papers by Ercan Demir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ercan Demir

This figure shows the co-authorship network connecting the top 25 collaborators of Ercan Demir. A scholar is included among the top collaborators of Ercan Demir 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 Demir. Ercan Demir 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
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Derinkuyu, Betül Emine, et al.. (2018). A child with atypically subtle clinical presentation of acute arterial ischaemic stroke in the middle cerebral artery. Interventional Neuroradiology. 24(6). 684–687. 1 indexed citations
3.
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Arhan, Ebru, Kıvılcım Gücüyener, Şebnem Soysal, et al.. (2017). Regional brain volume reduction and cognitive outcomes in preterm children at low risk at 9 years of age. Child s Nervous System. 33(8). 1317–1326. 29 indexed citations
5.
Gücüyener, Kıvılcım, et al.. (2017). Temporary Seizure in an Infant Who Had Been Exposed to G-Amino Butyric Acid Receptor Antagonist Thiocolchicoside. Pediatric Emergency Care. 35(5). e96–e97. 1 indexed citations
6.
Yılmaz, Ünsal, Bahadır Konuşkan, Kıvılcım Gücüyener, et al.. (2017). Multiple Sclerosis with Onset Younger Than 10 Years in Turkey. Neuropediatrics. 49(1). 51–58. 5 indexed citations
7.
Gücüyener, Kıvılcım, Necla Buyan, Ünsal Yılmaz, et al.. (2014). Does Nephrotoxicity Exist in Pediatric Epileptic Patients on Valproate or Carbamazepine Therapy?. Journal of Child Neurology. 30(3). 301–306. 7 indexed citations
8.
Yılmaz, Ünsal, et al.. (2012). Reduced Retinal Nerve Fiber Layer Thickness and Macular Volume in Pediatric Multiple Sclerosis. Journal of Child Neurology. 27(12). 1517–1523. 16 indexed citations
9.
Grossi, Serena, Stefano Regis, Roberta Biancheri, et al.. (2011). Molecular Genetic Analysis of the PLP1 Gene in 38 Families with PLP1-related disorders: Identification and Functional Characterization of 11 Novel PLP1 Mutations. Orphanet Journal of Rare Diseases. 6(1). 40–40. 32 indexed citations
10.
Demir, Ercan, et al.. (2010). Cardio-Facio-Cutaneous Syndrome: Phenotypic Variability and Differential Diagnosis in 3 Cases withde novoBRAF Mutations. Neuropediatrics. 41(3). 127–131. 4 indexed citations
11.
Demir, Ercan, et al.. (2009). Atypical Presentations of Subacute Sclerosing Panencephalitis in Two Neurologically Handicapped Cases. Neuropediatrics. 40(4). 195–198. 5 indexed citations
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Uyanık, G., Nursel Elçioğlu, Johannes Penzien, et al.. (2006). Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome. Neurology. 66(7). 1044–1048. 51 indexed citations
14.
Demir, Ercan. (2005). Giant axonal neuropathy: clinical and genetic study in six cases. Journal of Neurology Neurosurgery & Psychiatry. 76(6). 825–832. 43 indexed citations
15.
Demir, Ercan, Ana Ferreiro, Patrizia Sabatelli, et al.. (2004). Collagen VI Status and Clinical Severity in Ullrich Congenital Muscular Dystrophy: Phenotype Analysis of 11 Families Linked to theCOL6Loci. Neuropediatrics. 35(2). 103–112. 24 indexed citations
16.
Demir, Ercan, et al.. (2004). Infantile convulsions and paroxysmal choreoathetosis in a consanguineous family. Pediatric Neurology. 30(5). 349–353. 5 indexed citations
17.
Demir, Ercan, Patrizia Sabatelli, Valérie Allamand, et al.. (2002). Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy. The American Journal of Human Genetics. 70(6). 1446–1458. 119 indexed citations
18.
Bomont, Pascale, L Cavalier, F Blondeau, et al.. (2000). The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy. Nature Genetics. 26(3). 370–374. 313 indexed citations
19.
Cavalier, L, Rim Amouri, Samir Belal, et al.. (2000). Giant axonal neuropathy locus refinement to a < 590 kb critical interval. European Journal of Human Genetics. 8(7). 527–534. 18 indexed citations
20.
Kalaycı, Ömer, Turgay Coşkun, Ayşegül Tokatlı, et al.. (1994). Infantile spasms as the initial symptom of biotinidase deficiency. The Journal of Pediatrics. 124(1). 103–104. 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.

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