Melis Köse

694 total citations
42 papers, 195 citations indexed

About

Melis Köse is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Melis Köse has authored 42 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Clinical Biochemistry, 15 papers in Physiology and 14 papers in Molecular Biology. Recurrent topics in Melis Köse's work include Metabolism and Genetic Disorders (21 papers), Lysosomal Storage Disorders Research (9 papers) and Amino Acid Enzymes and Metabolism (6 papers). Melis Köse is often cited by papers focused on Metabolism and Genetic Disorders (21 papers), Lysosomal Storage Disorders Research (9 papers) and Amino Acid Enzymes and Metabolism (6 papers). Melis Köse collaborates with scholars based in Türkiye, United States and Cambodia. Melis Köse's co-authors include Ebru Canda, Sema Kalkan Uçar, Mahmut Çöker, Ünsal Yılmaz, Hüseyin Önay, Aycan Ünalp, Ferda Özkınay, Engi̇n Köse, Sara Habif and Taha Reşid Özdemir and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Seizure.

In The Last Decade

Melis Köse

39 papers receiving 190 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Melis Köse Türkiye 8 74 71 59 48 26 42 195
Fernanda Sperb‐Ludwig Brazil 11 97 1.3× 61 0.9× 100 1.7× 75 1.6× 47 1.8× 38 288
Vladimı́r Bzdúch Slovakia 8 103 1.4× 65 0.9× 83 1.4× 18 0.4× 25 1.0× 28 259
Alice Basinger United States 8 151 2.0× 47 0.7× 54 0.9× 23 0.5× 19 0.7× 11 275
Tanyel Zübarioğlu Türkiye 10 108 1.5× 121 1.7× 56 0.9× 16 0.3× 11 0.4× 52 281
Patrícia Janeiro Portugal 8 117 1.6× 89 1.3× 44 0.7× 22 0.5× 8 0.3× 20 213
Rebecca Mardach United States 11 193 2.6× 164 2.3× 100 1.7× 82 1.7× 57 2.2× 17 351
Serap Sivri Türkiye 11 120 1.6× 182 2.6× 145 2.5× 28 0.6× 18 0.7× 53 342
Vincenza Gragnaniello Italy 9 110 1.5× 34 0.5× 126 2.1× 22 0.5× 44 1.7× 31 254
Nawal Makhseed Kuwait 12 167 2.3× 104 1.5× 53 0.9× 15 0.3× 8 0.3× 18 303
Samia Pichard France 9 64 0.9× 64 0.9× 103 1.7× 28 0.6× 10 0.4× 25 193

Countries citing papers authored by Melis Köse

Since Specialization
Citations

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

Fields of papers citing papers by Melis Köse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melis Köse

This figure shows the co-authorship network connecting the top 25 collaborators of Melis Köse. A scholar is included among the top collaborators of Melis Köse 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 Melis Köse. Melis Köse 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.
Haroon, Suraiya, Heeyong Yoon, Christoph Seiler, et al.. (2023). N-acetylcysteine and cysteamine bitartrate prevent azide-induced neuromuscular decompensation by restoring glutathione balance in two novel surf1 −/− zebrafish deletion models of Leigh syndrome. Human Molecular Genetics. 32(12). 1988–2004. 8 indexed citations
2.
Albayrak, Hatice Mutlu, et al.. (2023). Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience. SHILAP Revista de lepidopterología. 10(3). 182–194.
3.
Taş, İbrahim, et al.. (2023). Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey. Molecular Genetics and Metabolism Reports. 36. 100979–100979. 4 indexed citations
4.
Yılmaz, Ünsal, et al.. (2022). The effectiveness of the ketogenic diet in drug-resistant childhood epilepsy. The Turkish Journal of Pediatrics. 64(2). 210–220. 4 indexed citations
5.
Ünalp, Aycan, et al.. (2022). A rare case of hypomyelinating leukodystrophy-14 benefiting from ketogenic diet therapy. The Turkish Journal of Pediatrics. 64(4). 747–753. 2 indexed citations
6.
Köse, Melis, et al.. (2022). A female case of 5,10-methenyltetrahydrofolate synthetase deficiency with novel neuro-imaging abnormalities. Brain and Development. 44(9). 640–644. 2 indexed citations
7.
Özkınay, Ferda, Melis Köse, Ebru Canda, et al.. (2021). Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel NAGLU gene mutations. Molecular Genetics and Metabolism Reports. 27. 100732–100732. 7 indexed citations
8.
Yılmaz, Ünsal, et al.. (2021). The effect of ketogenic diet on serum lipid concentrations in children with medication resistant epilepsy. Seizure. 91. 99–107. 18 indexed citations
9.
Köse, Melis, Engi̇n Köse, Aycan Ünalp, et al.. (2021). Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey. Neurological Sciences. 42(3). 1103–1111. 10 indexed citations
10.
Kulalı, Ferit, et al.. (2020). A new mutation associated with Pierson syndrome. Archivos Argentinos de Pediatria. 118(3). e288–e291. 3 indexed citations
11.
Köse, Engi̇n, et al.. (2020). Different clinical presentation in a patient with two novel pathogenic variants of the FBXL4 gene. The Turkish Journal of Pediatrics. 62(4). 652–656. 4 indexed citations
12.
Köse, Melis, et al.. (2020). Expanding the spectrum of VAC14 related pediatric-onset neurological disease; striatonigral degeneration with brainstem involvement. European Journal of Medical Genetics. 64(1). 104117–104117. 5 indexed citations
13.
Köse, Melis, et al.. (2020). A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey. The Turkish Journal of Pediatrics. 62(4). 647–651. 6 indexed citations
14.
Köse, Melis, Özlem Ünal, Burcu Öztürk Hişmi, et al.. (2019). Clinical and molecular characteristics and time of diagnosis of patients with classical galactosemia in an unscreened population in Turkey. Journal of Pediatric Endocrinology and Metabolism. 32(7). 675–681. 4 indexed citations
15.
Köse, Melis, et al.. (2019). Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13. Journal of Pediatric Endocrinology and Metabolism. 33(1). 157–163. 10 indexed citations
16.
Köse, Melis, Gülçin Akıncı, Cenk Eraslan, et al.. (2018). The Second Case of Saposin A Deficiency and Altered Autophagy. JIMD Reports. 44. 43–54. 6 indexed citations
17.
Köse, Melis, Ebru Canda, Sema Kalkan Uçar, et al.. (2018). Coexistence of Gaucher Disease and severe congenital neutropenia. Blood Cells Molecules and Diseases. 76. 1–6. 3 indexed citations
18.
Canda, Ebru, Havva Yazıcı, Melis Köse, et al.. (2018). Single center experience of biotinidase deficiency: 259 patients and six novel mutations. Journal of Pediatric Endocrinology and Metabolism. 31(8). 917–926. 27 indexed citations
19.
Köse, Melis, et al.. (2017). A Patient with MSUD: Acute Management with Sodium Phenylacetate/Sodium Benzoate and Sodium Phenylbutyrate. SHILAP Revista de lepidopterología. 2017(1). 1045031–1045031. 5 indexed citations
20.
Uçar, Sema Kalkan, Burcu Özbaran, Yasemin Atik Altınok, et al.. (2014). One Year Experience of Pheburane® (Sodium Phenylbutyrate) Treatment in a Patient with Argininosuccinate Lyase Deficiency. JIMD Reports. 19. 31–33. 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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