Hayat Erdem‐Yurter

724 total citations
38 papers, 553 citations indexed

About

Hayat Erdem‐Yurter is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Hayat Erdem‐Yurter has authored 38 papers receiving a total of 553 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 18 papers in Genetics and 7 papers in Surgery. Recurrent topics in Hayat Erdem‐Yurter's work include Neurogenetic and Muscular Disorders Research (18 papers), RNA modifications and cancer (16 papers) and RNA Research and Splicing (6 papers). Hayat Erdem‐Yurter is often cited by papers focused on Neurogenetic and Muscular Disorders Research (18 papers), RNA modifications and cancer (16 papers) and RNA Research and Splicing (6 papers). Hayat Erdem‐Yurter collaborates with scholars based in Türkiye, Germany and United Kingdom. Hayat Erdem‐Yurter's co-authors include Gamze Bora, Didem Dayangaç Erden, Sevim Dalkara, Ayhan S. Demir, Kemal Yelekçi, Meral Özgüç, Engin Yılmaz, Ayşen Karaduman, Haluk Topaloğlu and Turgay Coşkun and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Human Reproduction.

In The Last Decade

Hayat Erdem‐Yurter

36 papers receiving 535 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hayat Erdem‐Yurter Türkiye 13 326 111 79 59 55 38 553
Yingmin Zhang China 11 346 1.1× 54 0.5× 49 0.6× 55 0.9× 35 0.6× 30 562
Brian K. Park United States 9 222 0.7× 37 0.3× 30 0.4× 48 0.8× 16 0.3× 14 552
Inan Olmez United States 11 249 0.8× 106 1.0× 55 0.7× 42 0.7× 161 2.9× 14 696
E Liong Hong Kong 11 177 0.5× 26 0.2× 34 0.4× 30 0.5× 42 0.8× 15 429
Jacques Chevalier France 15 163 0.5× 65 0.6× 20 0.3× 16 0.3× 51 0.9× 19 483
Natanael Zarco United States 15 208 0.6× 77 0.7× 41 0.5× 31 0.5× 48 0.9× 30 531
Liming Wang China 16 266 0.8× 23 0.2× 29 0.4× 19 0.3× 36 0.7× 43 619
Hideji Yako Japan 16 301 0.9× 31 0.3× 13 0.2× 46 0.8× 43 0.8× 39 625
Shigeru Kanaoka Japan 11 209 0.6× 26 0.2× 102 1.3× 39 0.7× 65 1.2× 28 617
Yanlian Xiong China 13 214 0.7× 68 0.6× 17 0.2× 27 0.5× 43 0.8× 31 478

Countries citing papers authored by Hayat Erdem‐Yurter

Since Specialization
Citations

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

Fields of papers citing papers by Hayat Erdem‐Yurter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hayat Erdem‐Yurter. 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 Hayat Erdem‐Yurter. The network helps show where Hayat Erdem‐Yurter may publish in the future.

Co-authorship network of co-authors of Hayat Erdem‐Yurter

This figure shows the co-authorship network connecting the top 25 collaborators of Hayat Erdem‐Yurter. A scholar is included among the top collaborators of Hayat Erdem‐Yurter 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 Hayat Erdem‐Yurter. Hayat Erdem‐Yurter 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.
Bal, Sevgi Köstel, Gamze Bora, Beril Talim, et al.. (2022). Alterations in insulin‐like growth factor system in spinal muscular atrophy. Muscle & Nerve. 66(5). 631–638. 6 indexed citations
2.
Bora, Gamze, Niko Hensel, Sebastian Rademacher, et al.. (2020). Microtubule-associated protein 1B dysregulates microtubule dynamics and neuronal mitochondrial transport in spinal muscular atrophy. Human Molecular Genetics. 29(24). 3935–3944. 16 indexed citations
3.
Bora, Gamze, et al.. (2019). Class I histone deacetylase inhibition by aryl butenoic acid derivatives: In silico and in vitro studies. Journal of Research in Pharmacy. 23(5). 952–959. 1 indexed citations
4.
Bora, Gamze, et al.. (2018). Effects of Arm Cycling Exercise in Spinal Muscular Atrophy Type II Patients: A Pilot Study. Journal of Child Neurology. 33(3). 209–215. 20 indexed citations
5.
Bora, Gamze, et al.. (2015). Spinal muscular atrophy type III: Molecular genetic characterization of Turkish patients. European Journal of Medical Genetics. 58(12). 654–658. 5 indexed citations
6.
Bora, Gamze & Hayat Erdem‐Yurter. (2014). Investigations of Curcumin and Resveratrol on Neurite Outgrowth: Perspectives on Spinal Muscular Atrophy. BioMed Research International. 2014. 1–8. 15 indexed citations
7.
Uzunallı, Gözde, Gamze Bora, Didem Dayangaç Erden, & Hayat Erdem‐Yurter. (2014). Effects of flavonoid quercetin on survival of motor neuron gene expression. Cell Biology International. 39(3). 350–354. 6 indexed citations
8.
Bora, Gamze, et al.. (2011). Power of inhibition activity screening and 3D molecular modeling approaches in HDAC 8 inhibitor design. TURKISH JOURNAL OF CHEMISTRY. 3 indexed citations
9.
Erden, Didem Dayangaç, Gamze Bora, Sevim Dalkara, Ayhan S. Demir, & Hayat Erdem‐Yurter. (2011). Carboxylic acid derivatives of histone deacetylase inhibitors induce full length SMN2 transcripts: a promising target for spinal muscular atrophy therapeutics. Archives of Medical Science. 2(2). 230–234. 12 indexed citations
10.
Tanrıöver, Mine Durusu, Gamze Bora, Didem Dayangaç Erden, et al.. (2010). Evaluation of the effects of vitamin D receptor and estrogen receptor 1 gene polymorphisms on bone mineral density in postmenopausal women. Clinical Rheumatology. 29(11). 1285–1293. 26 indexed citations
11.
Bora, Gamze, Didem Dayangaç Erden, Ayhan S. Demir, et al.. (2009). Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies. Bioorganic & Medicinal Chemistry. 17(14). 5219–5228. 138 indexed citations
12.
Erden, Didem Dayangaç, Gamze Bora, Çetin Kocaefe, et al.. (2009). Histone Deacetylase Inhibition Activity and Molecular Docking of (E )‐Resveratrol: Its Therapeutic Potential in Spinal Muscular Atrophy. Chemical Biology & Drug Design. 73(3). 355–364. 38 indexed citations
13.
Erden, Didem Dayangaç, Haluk Topaloğlu, & Hayat Erdem‐Yurter. (2008). A preliminary report on spinal muscular atrophy lymphoblastoid cell lines: Are they an appropriate tool for drug screening?. Advances in Therapy. 25(3). 274–279. 4 indexed citations
14.
Erdem‐Yurter, Hayat, Engin Yılmaz, Ahmet Şahin, et al.. (2004). Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens. Human Reproduction. 19(5). 1094–1100. 41 indexed citations
15.
Özbas‐Gerçeker, Filiz, Uğur Özçelik, Nural Ki̇per, et al.. (2002). Analysis of the modifying effects of TAP 1/2 genes on cystic fibrosis phenotype.. PubMed. 44(2). 91–7. 3 indexed citations
16.
Özgül, Rıza Köksal, Caroline Paternotte, Hayat Erdem‐Yurter, et al.. (2001). Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in Two Unrelated Turkish Families. Neuropediatrics. 32(3). 142–146. 24 indexed citations
17.
Topaloğlu, Haluk, Faruk Güçlü Pınarlı, Hayat Erdem‐Yurter, et al.. (1998). Clinical Observations in Autosomal Recessive Spastic Paraplegia in Childhood and Further Evidence for Genetic Heterogeneity. Neuropediatrics. 29(4). 189–194. 4 indexed citations
18.
Yılmaz, Engin, et al.. (1995). Study of 12 Mutations in Turkish Cystic Fibrosis Patients. Human Heredity. 45(3). 175–177. 23 indexed citations
19.
Özgüç, Meral, Engin Yılmaz, Hayat Erdem‐Yurter, et al.. (1994). Allele frequencies of Mp6D‐9 and GATT markers in 32 Turkish cystic fibrosis families. Clinical Genetics. 45(5). 266–268.
20.
Özgüç, Meral, Ali Tekin, Hayat Erdem‐Yurter, et al.. (1994). Analysis of ΔF508 Mutation in Cystic Fibrosis Pathology Specimens. Pediatric Pathology. 14(3). 491–496. 1 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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