Sefer Kumandaş

2.9k total citations
100 papers, 1.5k citations indexed

About

Sefer Kumandaş is a scholar working on Surgery, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Sefer Kumandaş has authored 100 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Surgery, 21 papers in Pediatrics, Perinatology and Child Health and 19 papers in Genetics. Recurrent topics in Sefer Kumandaş's work include Pharmacological Effects and Toxicity Studies (11 papers), Epilepsy research and treatment (9 papers) and Metabolism and Genetic Disorders (7 papers). Sefer Kumandaş is often cited by papers focused on Pharmacological Effects and Toxicity Studies (11 papers), Epilepsy research and treatment (9 papers) and Metabolism and Genetic Disorders (7 papers). Sefer Kumandaş collaborates with scholars based in Türkiye, United States and Japan. Sefer Kumandaş's co-authors include Hakan Gümüş, Hüseyin Per, Mehmet Canpolat, Ali Yıkılmaz, Abdulhakim Çoşkun, Ali Kurtsoy, Hatice Gamze Poyrazoğlu, Ayşe Kaçar Bayram, Selim Kurtoğlu and Mustafa Akçakuş and has published in prestigious journals such as SHILAP Revista de lepidopterología, Developmental Medicine & Child Neurology and European Radiology.

In The Last Decade

Sefer Kumandaş

91 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sefer Kumandaş Türkiye 24 371 334 258 228 227 100 1.5k
Hakan Gümüş Türkiye 24 336 0.9× 299 0.9× 245 0.9× 200 0.9× 143 0.6× 106 1.6k
Hüseyin Per Türkiye 24 249 0.7× 328 1.0× 302 1.2× 197 0.9× 148 0.7× 132 1.7k
Veena Kalra India 20 314 0.8× 416 1.2× 134 0.5× 241 1.1× 138 0.6× 105 1.3k
Manuel Castro‐Gago Spain 21 471 1.3× 413 1.2× 91 0.4× 367 1.6× 173 0.8× 105 1.4k
Hideto Yoshikawa Japan 18 257 0.7× 267 0.8× 120 0.5× 230 1.0× 134 0.6× 74 1.3k
Ching‐Shiang Chi Taiwan 22 248 0.7× 251 0.8× 89 0.3× 477 2.1× 120 0.5× 134 1.5k
Eli Heyman Israel 19 397 1.1× 343 1.0× 94 0.4× 102 0.4× 123 0.5× 48 1.2k
Cengiz Yakıncı Türkiye 17 180 0.5× 165 0.5× 94 0.4× 152 0.7× 79 0.3× 90 892
L. T. Kurland United States 16 164 0.4× 335 1.0× 547 2.1× 165 0.7× 83 0.4× 28 1.5k
Keisuke Ishii Japan 29 1.0k 2.8× 181 0.5× 725 2.8× 486 2.1× 87 0.4× 204 3.1k

Countries citing papers authored by Sefer Kumandaş

Since Specialization
Citations

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

Fields of papers citing papers by Sefer Kumandaş

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sefer Kumandaş

This figure shows the co-authorship network connecting the top 25 collaborators of Sefer Kumandaş. A scholar is included among the top collaborators of Sefer Kumandaş 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 Sefer Kumandaş. Sefer Kumandaş 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.
Erdoğan, Murat, Hakan Gümüş, Ahmet Sami Güven, et al.. (2025). A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis. Neurogenetics. 26(1). 47–47.
2.
3.
Canpolat, Mehmet, Fatih Kardaş, Mustafa Kendırcı, et al.. (2022). Serum Vitamin D and B12 Levels in School-aged Children and Adolescents with Frequent Primary Headache Attacks. SHILAP Revista de lepidopterología. 3(4). 149–155.
4.
Canpolat, Mehmet, Hüseyin Per, Abdulhakim Çoşkun, et al.. (2021). Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome. Turkish Archives of Pediatrics. 56(6). 569–575.
5.
Demi̇rci̇, Esra, et al.. (2019). Levels of Salivary Sialic Acid in Children with Autism Spectrum Disorder; Could It Be Related to Stereotypes and Hyperactivity?. Clinical Psychopharmacology and Neuroscience. 17(3). 415–422. 12 indexed citations
6.
Kumandaş, Sefer, Niyazi Acer, Selim Doğanay, et al.. (2017). Evaluating brainstem in breath-holding spells. European Journal of Paediatric Neurology. 21. e78–e78.
7.
Bayram, Ayşe Kaçar, Mehmet Canpolat, Hakan Gümüş, et al.. (2015). Misdiagnosis of gastroesophageal reflux disease as epileptic seizures in children. Brain and Development. 38(3). 274–279. 9 indexed citations
8.
Bayraklı, Fatih, Hatice Gamze Poyrazoğlu, Cengiz Yakıcıer, et al.. (2015). Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene. Journal of Human Genetics. 60(12). 763–768. 17 indexed citations
9.
Canpolat, Mehmet, Sefer Kumandaş, Hatice Gamze Poyrazoğlu, et al.. (2014). Prevalence and risk factors of epilepsy among school children in Kayseri City Center, an urban area in Central Anatolia, Turkey. Seizure. 23(9). 708–716. 26 indexed citations
10.
Poyrazoğlu, Hatice Gamze, Sefer Kumandaş, Mehmet Canpolat, et al.. (2014). The Prevalence of Migraine and Tension-Type Headache Among Schoolchildren in Kayseri, Turkey. Journal of Child Neurology. 30(7). 889–895. 23 indexed citations
11.
Per, Hüseyin, Mehmet Canpolat, Hakan Gümüş, et al.. (2013). Different etiologies of acquired torticollis in childhood. Child s Nervous System. 30(3). 431–440. 30 indexed citations
12.
Canpolat, Mehmet, Hüseyin Per, Ali Yıkılmaz, et al.. (2013). Sturge-Weber syndrome: clinical and radiological evaluation. DergiPark (Istanbul University). 19(1). 30–30.
13.
Eki̇ci̇, Mehmet, et al.. (2011). Concomitant heart and brain hydatid cyst without other organ involvement: a case report / Diğer organların tutulumu olmaksızın eş zamanlı kalp ve beynin kist hidatik tutulumu: Olgu bildirimi. Dusunen Adam The Journal of Psychiatry and Neurological Sciences. 155–159. 2 indexed citations
14.
Gümüş, Hakan, Hüseyin Per, Meda Kondolot, et al.. (2010). Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency. Developmental Medicine & Child Neurology. 52(9). 868–872. 15 indexed citations
15.
Yıkılmaz, Ali, et al.. (2010). Magnetic resonance imaging of childhood Guillain–Barré syndrome. Child s Nervous System. 26(9). 1137–1137.
16.
Per, Hüseyin, Sefer Kumandaş, Hakan Gümüş, Mustafa Öztürk, & Abdulhakim Çoşkun. (2008). Meningitis and Subgaleal, Subdural, Epidural Empyema Due to Pasteurella Multocida. Journal of Emergency Medicine. 39(1). 35–38. 21 indexed citations
17.
Per, Hüseyin, Sefer Kumandaş, Abdulhakim Çoşkun, Hakan Gümüş, & Didem Behice Öztop. (2008). Neurologic Sequelae of Neonatal Hypoglycemia in Kayseri, Turkey. Journal of Child Neurology. 23(12). 1406–1412. 16 indexed citations
18.
Kumandaş, Sefer, Ali Kurtsoy, Özlem Canöz, et al.. (2006). Erdheim Chester disease: Cerebral involvement in childhood. Brain and Development. 29(4). 227–230. 11 indexed citations
19.
Akçakuş, Mustafa, Tamer Güneş, Sefer Kumandaş, Selim Kurtoğlu, & Abdulhakim Çoşkun. (2003). Joubert syndrome: Report of a neonatal case. Paediatrics & Child Health. 8(8). 499–502. 16 indexed citations
20.
Kurtoğlu, Selim, et al.. (2000). Patient with Weismann-Netter and Stuhl (Toxopachyosteosis) Syndrome with Communicant Hydrocephalus and Arachnoid Cyst. Journal of Pediatric Endocrinology and Metabolism. 13(2). 211–5. 4 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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