Adnan Yüksel

2.1k total citations
62 papers, 971 citations indexed

About

Adnan Yüksel is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Adnan Yüksel has authored 62 papers receiving a total of 971 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Pediatrics, Perinatology and Child Health and 16 papers in Genetics. Recurrent topics in Adnan Yüksel's work include Epilepsy research and treatment (14 papers), Pharmacological Effects and Toxicity Studies (12 papers) and RNA regulation and disease (7 papers). Adnan Yüksel is often cited by papers focused on Epilepsy research and treatment (14 papers), Pharmacological Effects and Toxicity Studies (12 papers) and RNA regulation and disease (7 papers). Adnan Yüksel collaborates with scholars based in Türkiye, United States and Germany. Adnan Yüksel's co-authors include Mehmet Seven, Müjgan Cengiz, Turgut Ulutin, Bayram Yılmaz, Gözde Yeşil, Asım Cenani, Ülkan Kılıç, Bahadır Batar, Mehmet Güven and Dirk M. Hermann and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neuroscience and Human Molecular Genetics.

In The Last Decade

Adnan Yüksel

61 papers receiving 948 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adnan Yüksel Türkiye 17 336 314 251 127 118 62 971
Mehmet Seven Türkiye 15 265 0.8× 304 1.0× 196 0.8× 115 0.9× 62 0.5× 59 765
Maura Casalgrandi Italy 5 127 0.4× 402 1.3× 262 1.0× 88 0.7× 110 0.9× 6 1.4k
Marvin Peters Germany 21 132 0.4× 690 2.2× 90 0.4× 87 0.7× 114 1.0× 51 1.4k
Mutlu Küçük Türkiye 20 119 0.4× 266 0.8× 114 0.5× 31 0.2× 152 1.3× 51 1.1k
Vidar M. Steen Norway 14 91 0.3× 354 1.1× 170 0.7× 190 1.5× 106 0.9× 25 969
Leslie Schwendimann France 22 444 1.3× 325 1.0× 53 0.2× 29 0.2× 91 0.8× 40 1.2k
Maurice Abramow Belgium 17 185 0.6× 834 2.7× 48 0.2× 90 0.7× 232 2.0× 46 1.5k
Yukio Nishizawa Japan 13 203 0.6× 390 1.2× 237 0.9× 59 0.5× 85 0.7× 27 1.4k
Yusuke Sagara Japan 20 261 0.8× 231 0.7× 33 0.1× 243 1.9× 154 1.3× 58 1.1k
Virginia Hovanesian United States 13 76 0.2× 370 1.2× 113 0.5× 39 0.3× 791 6.7× 18 1.4k

Countries citing papers authored by Adnan Yüksel

Since Specialization
Citations

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

Fields of papers citing papers by Adnan Yüksel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adnan Yüksel

This figure shows the co-authorship network connecting the top 25 collaborators of Adnan Yüksel. A scholar is included among the top collaborators of Adnan Yüksel 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 Adnan Yüksel. Adnan Yüksel 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.
Lee, Byeonghyeon, Mehmet Buğrahan Düz, Asuman Koparır, et al.. (2015). Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome. Gene. 576(2). 776–781. 5 indexed citations
2.
Weaver, K. Nicole, Robert J. Hopkin, Kristen L. Sund, et al.. (2014). Keutel syndrome: Report of two novel MGP mutations and discussion of clinical overlap with arylsulfatase E deficiency and relapsing polychondritis. American Journal of Medical Genetics Part A. 164(4). 1062–1068. 15 indexed citations
3.
Demirkol, Demet, et al.. (2014). Therapeutic Plasma Exchange for Malignant Refractory Status Epilepticus: A Case Report. Pediatric Neurology. 50(4). 407–410. 13 indexed citations
4.
5.
Karataş, Ömer Faruk, et al.. (2013). MicroRNA profiling in lymphocytes and serum of tyrosinemia type-I patients. Molecular Biology Reports. 40(7). 4619–4623. 6 indexed citations
6.
Gezdirici, Alper, Alper Yenigün, Erkan Koparir, et al.. (2012). A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia. Clinical Dysmorphology. 22(1). 33–35. 2 indexed citations
7.
Karaca, Emin, et al.. (2011). Sudden vision loss in a mucopolysaccharidosis I patient receiving enzyme replacement therapy.. PubMed. 22(4). 371–6. 3 indexed citations
8.
Kılıç, Ülkan, Bayram Yılmaz, Milas Ugur, et al.. (2011). Evidence that membrane‐bound G protein‐coupled melatonin receptors MT1 and MT2 are not involved in the neuroprotective effects of melatonin in focal cerebral ischemia. Journal of Pineal Research. 52(2). 228–235. 99 indexed citations
9.
Albayram, Sait, et al.. (2008). Spontaneous Intracranial Hypotension Syndrome in a Patient With Marfan Syndrome and Autosomal Dominant Polycystic Kidney Disease. Headache The Journal of Head and Face Pain. 48(4). 632–636. 9 indexed citations
10.
Yüksel, Adnan, et al.. (2007). Supernumerary chromosome der(22)t(11;22): Emanuel syndrome associates with novel features.. PubMed. 18(4). 401–8. 4 indexed citations
11.
Yüksel, Adnan, et al.. (2006). Facial Dysmorphism in Leigh Syndrome With SURF-1 Mutation and COX Deficiency. Pediatric Neurology. 34(6). 486–489. 14 indexed citations
12.
Yalçınkaya, Cengiz, et al.. (2003). Epilepsy in vacuolating megalencephalic leukoencephalopathy with subcortical cysts. Seizure. 12(6). 388–396. 21 indexed citations
13.
Seven, Mehmet, et al.. (2002). A case of acampomelic campomelic dysplasia.. PubMed. 13(1). 23–8. 3 indexed citations
14.
Yüksel, Adnan, Müjgan Cengiz, Mehmet Seven, & Turgut Ulutin. (2000). Erythrocyte Glutathione, Glutathione Peroxidase, Superoxide Dismutase and Serum Lipid Peroxidation in Epileptic Children With Valproate and Carbamazepine Monotherapy. Journal of Basic and Clinical Physiology and Pharmacology. 11(1). 73–81. 69 indexed citations
15.
Yalçınkaya, Cengiz, et al.. (2000). Siblings With Cystic Leukoencephalopathy and Megalencephaly. Journal of Child Neurology. 15(10). 690–693. 6 indexed citations
16.
Soylu, Hanifi, et al.. (2000). Infantile‐onset megalencephalic leucoencephalopathy in two siblings. Journal of Paediatrics and Child Health. 36(6). 598–602. 2 indexed citations
17.
Seven, Mehmet, et al.. (1999). A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations.. PubMed. 40(4). 593–601. 1 indexed citations
18.
Yüksel, Adnan, et al.. (1997). The extent of leprosy-related disabilities in Istanbul Leprosy Hospital, Turkey. Leprosy Review. 68(1). 43–9. 6 indexed citations
19.
Yüksel, Adnan, et al.. (1993). Serum thyroid hormones and pituitary response to thyrotropin‐releasing hormone in epileptic children receiving anti‐epileptic medication. Pediatrics International. 35(2). 108–112. 22 indexed citations
20.
Yüksel, Adnan, et al.. (1993). Influence of long‐term carbamazepine treatment on thyroid function. Pediatrics International. 35(3). 229–232. 12 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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