E. Zeynep Erson‐Omay

4.0k total citations
35 papers, 242 citations indexed

About

E. Zeynep Erson‐Omay is a scholar working on Neurology, Epidemiology and Surgery. According to data from OpenAlex, E. Zeynep Erson‐Omay has authored 35 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Neurology, 13 papers in Epidemiology and 9 papers in Surgery. Recurrent topics in E. Zeynep Erson‐Omay's work include Meningioma and schwannoma management (10 papers), Neurofibromatosis and Schwannoma Cases (10 papers) and Glioma Diagnosis and Treatment (8 papers). E. Zeynep Erson‐Omay is often cited by papers focused on Meningioma and schwannoma management (10 papers), Neurofibromatosis and Schwannoma Cases (10 papers) and Glioma Diagnosis and Treatment (8 papers). E. Zeynep Erson‐Omay collaborates with scholars based in United States, Germany and China. E. Zeynep Erson‐Omay's co-authors include Murat Günel, Jennifer Moliterno, Robert K. Fulbright, Anita Hüttner, Elena I. Fomchenko, Christopher S. Hong, Hang Cao, Katsuhito Yasuno, Xuejun Li and Lan Jin and has published in prestigious journals such as Neurology, Journal of neurosurgery and Journal of Hepatology.

In The Last Decade

E. Zeynep Erson‐Omay

34 papers receiving 240 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Zeynep Erson‐Omay United States 10 77 65 64 52 48 35 242
Ayça Erşen Danyeli Türkiye 9 120 1.6× 52 0.8× 66 1.0× 87 1.7× 69 1.4× 49 273
Yukitomo Ishi Japan 11 129 1.7× 31 0.5× 93 1.5× 52 1.0× 85 1.8× 55 316
Balázs Murnyák Hungary 9 79 1.0× 62 1.0× 116 1.8× 104 2.0× 60 1.3× 23 324
Angela Guerriero Italy 10 35 0.5× 31 0.5× 96 1.5× 42 0.8× 25 0.5× 26 277
Melissa Umphlett United States 11 103 1.3× 38 0.6× 53 0.8× 129 2.5× 93 1.9× 30 268
Tzu-Kang Lin Taiwan 7 60 0.8× 105 1.6× 66 1.0× 42 0.8× 129 2.7× 9 299
Janice Brewer Australia 10 109 1.4× 28 0.4× 119 1.9× 57 1.1× 46 1.0× 20 397
Jaejoon Lim South Korea 12 63 0.8× 86 1.3× 127 2.0× 96 1.8× 29 0.6× 40 368
Shengyue Huang China 9 115 1.5× 30 0.5× 63 1.0× 52 1.0× 73 1.5× 18 271
Toshikazu Hidaka Japan 10 34 0.4× 51 0.8× 86 1.3× 31 0.6× 104 2.2× 42 291

Countries citing papers authored by E. Zeynep Erson‐Omay

Since Specialization
Citations

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

Fields of papers citing papers by E. Zeynep Erson‐Omay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. Zeynep Erson‐Omay. 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. Zeynep Erson‐Omay. The network helps show where E. Zeynep Erson‐Omay may publish in the future.

Co-authorship network of co-authors of E. Zeynep Erson‐Omay

This figure shows the co-authorship network connecting the top 25 collaborators of E. Zeynep Erson‐Omay. A scholar is included among the top collaborators of E. Zeynep Erson‐Omay 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. Zeynep Erson‐Omay. E. Zeynep Erson‐Omay 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.
Mehta, Neel H., Eduardo A. Maury, Phan Q. Duy, et al.. (2024). Genetics and molecular pathophysiology of normal pressure hydrocephalus. Journal of neurosurgery. 142(2). 1–7. 2 indexed citations
2.
Marianayagam, Neelan J., Zachary Corbin, Declan McGuone, et al.. (2023). The clinical and genomic features of seizures in meningiomas. Neuro-Oncology Advances. 5(Supplement_1). i49–i57. 9 indexed citations
3.
Barak, Tanyeri, Ketu Mishra-Gorur, Danielle Miyagishima, et al.. (2022). Clinical Implications of the Genomic Profiling of Sporadic Multiple Meningiomas. Journal of Neurological Surgery Part B Skull Base. 83(S 01). S1–S270. 1 indexed citations
4.
Fomchenko, Elena I., Benjamin C. Reeves, William Sullivan, et al.. (2021). Dual activating FGFR1 mutations in pediatric pilomyxoid astrocytoma. Molecular Genetics & Genomic Medicine. 9(2). e1597–e1597. 3 indexed citations
5.
Hong, Christopher S., Aladine A. Elsamadicy, Silvio E. Inzucchi, et al.. (2021). Comprehensive Genomic Characterization of A Case of Granular Cell Tumor of the Posterior Pituitary Gland: A Case Report. Frontiers in Endocrinology. 12. 762095–762095. 7 indexed citations
6.
Hong, Christopher S., Adam J. Kundishora, Aladine A. Elsamadicy, et al.. (2021). Somatic NF1 mutations in pituitary adenomas: Report of two cases. Cancer Genetics. 256-257. 26–30. 4 indexed citations
7.
Hong, Christopher S., E. Zeynep Erson‐Omay, & Jennifer Moliterno. (2021). Multiple meningiomas arising within the same hemisphere associated with Li-Fraumeni syndrome. Surgical Neurology International. 12. 99–99. 1 indexed citations
8.
Robert, Stephanie M., Mark W. Youngblood, Lan Jin, et al.. (2021). The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications. Journal of Neuro-Oncology. 156(2). 205–214. 15 indexed citations
9.
Hong, Christopher S., Yi An, Pallavi P. Gopal, et al.. (2020). Genetic characterization of an aggressive optic nerve pilocytic glioma. Brain Tumor Pathology. 38(1). 59–63. 2 indexed citations
10.
Kaulen, Leon D., E. Zeynep Erson‐Omay, Octavian Henegariu, et al.. (2020). Whole Exome Sequencing Identifies Novel SLIT2 Mutations in Primary CNS Lymphoma (3962). Neurology. 94(15_supplement).
11.
Karschnia, Philipp, E. Zeynep Erson‐Omay, Anita Hüttner, et al.. (2020). Genomic alterations in Turcot syndrome: Insights from whole exome sequencing. Journal of the Neurological Sciences. 417. 117056–117056. 1 indexed citations
12.
Fomchenko, Elena I., E. Zeynep Erson‐Omay, Adam J. Kundishora, et al.. (2020). Genomic alterations underlying spinal metastases in pediatric H3K27M-mutant pineal parenchymal tumor of intermediate differentiation: case report. Journal of Neurosurgery Pediatrics. 25(2). 121–130. 10 indexed citations
13.
Cao, Hang, E. Zeynep Erson‐Omay, Xuejun Li, et al.. (2020). A quantitative model based on clinically relevant MRI features differentiates lower grade gliomas and glioblastoma. European Radiology. 30(6). 3073–3082. 23 indexed citations
14.
Fomchenko, Elena I., E. Zeynep Erson‐Omay, Amy Zhao, et al.. (2019). DNMT3A co-mutation in an IDH1-mutant glioblastoma. Molecular Case Studies. 5(4). a004119–a004119. 7 indexed citations
15.
Jin, Lan, Yawei Zhang, Wyatt B. David, et al.. (2019). Extent of resection of epidermoid tumors and risk of recurrence: case report and meta-analysis. Journal of neurosurgery. 133(2). 291–301. 24 indexed citations
16.
Fomchenko, Elena I., Daniel Durán, Sheng Chih Jin, et al.. (2018). De novo MYH9 mutation in congenital scalp hemangioma. Molecular Case Studies. 4(4). a002998–a002998. 7 indexed citations
17.
Akyerli, Cemaliye Boylu, E. Zeynep Erson‐Omay, Yavuz Oktay, et al.. (2017). Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas. Journal of neurosurgery. 128(4). 1102–1114. 25 indexed citations
18.
Vilarinho, Sílvia, E. Zeynep Erson‐Omay, Kisha Mitchell-Richards, et al.. (2017). Exome analysis of the evolutionary path of hepatocellular adenoma-carcinoma transition, vascular invasion and brain dissemination. Journal of Hepatology. 67(1). 186–191. 8 indexed citations
19.
Çağlayan, Ahmet Okay, Beyhan Tüysüz, Süleyman Coşkun, et al.. (2016). A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP. Journal of Human Genetics. 61(5). 395–403. 13 indexed citations
20.
Vilarinho, Sílvia, E. Zeynep Erson‐Omay, Akdes Serin Harmancı, et al.. (2014). Paediatric hepatocellular carcinoma due to somatic CTNNB1 and NFE2L2 mutations in the setting of inherited bi-allelic ABCB11 mutations. Journal of Hepatology. 61(5). 1178–1183. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ayça Erşen Danyeli Breakdown of academic impact, for papers by Yukitomo Ishi Breakdown of academic impact, for papers by Balázs Murnyák Breakdown of academic impact, for papers by Angela Guerriero Breakdown of academic impact, for papers by Melissa Umphlett Breakdown of academic impact, for papers by Tzu-Kang Lin Breakdown of academic impact, for papers by Janice Brewer Breakdown of academic impact, for papers by Jaejoon Lim Breakdown of academic impact, for papers by Shengyue Huang Breakdown of academic impact, for papers by Toshikazu Hidaka
Rankless by CCL
2026