Ayşegül Tokatlı
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders 58
- Biochemistry top 5%
- Cell Biology top 5%
- Biotin and Related Studies 11
- Rheumatology top 5%
- Folate and B Vitamins Research 13
- Physiology top 10%
- Lysosomal Storage Disorders Research 11
- Diet and metabolism studies 10
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- Mitochondrial Function and Pathology 21
- Biochemical and Molecular Research 12
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- Neonatal Health and Biochemistry 14
- Co-authors
- Turgay Coşkunİ ÖzalpAli DursunHatice Serap SivriYılmaz YıldızRıza Köksal ÖzgülH. Serap KalkanoğluHaluk Topaloğlu
- Journals
- Journal of Inherited Metabolic Disease (16 papers)Molecular Genetics and Metabolism (5 papers)Journal of Child Neurology (4 papers)
- Partner nations
- TürkiyeUnited StatesGermany
In The Last Decade
Ayşegül Tokatlı
96 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 82
- Clinical Biochemistry 575
- Biochemistry 146
- Cell Biology 254
- Rheumatology 184
- Physiology 249
Countries citing papers authored by Ayşegül Tokatlı
This map shows the geographic impact of Ayşegül Tokatlı'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 Ayşegül Tokatlı with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ayşegül Tokatlı more than expected).
Fields of papers citing papers by Ayşegül Tokatlı
This network shows the impact of papers produced by Ayşegül Tokatlı. 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 Ayşegül Tokatlı. The network helps show where Ayşegül Tokatlı may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Ayşegül Tokatlı, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 2 | |
| 2 | 2021 | 8 | |
| 3 | 2021 | 1 | |
| 4 | 2021 | 1 | |
| 5 | 2018 | 10 | |
| 6 | Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation. | 2017 | 6 |
| 7 | A Nonvirilized form of Classic 3[beta]-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria | 2016 | 1 |
| 8 | Sapropterin dihydrochloride treatment in Turkish hyperphenylalaninemic patients under age four. | 2016 | 7 |
| 9 | 2016 | 9 | |
| 10 | 2013 | 6 | |
| 11 | 2013 | 9 | |
| 12 | 2012 | 2 | |
| 13 | 2011 | 9 | |
| 14 | 2011 | 20 | |
| 15 | 2011 | 46 | |
| 16 | 2007 | 33 | |
| 17 | 2006 | 9 | |
| 18 | 2005 | 34 | |
| 19 | 2002 | 21 | |
| 20 | 2002 | 25 |
About Ayşegül Tokatlı
Ayşegül Tokatlı is a scholar working on Clinical Biochemistry, Biochemistry, Rheumatology, Cell Biology and Pediatrics, Perinatology and Child Health, having authored 101 papers that have together received 1.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (58 papers), Mitochondrial Function and Pathology (21 papers), Neonatal Health and Biochemistry (14 papers), Folate and B Vitamins Research (13 papers), Biochemical and Molecular Research (12 papers), Biotin and Related Studies (11 papers), Lysosomal Storage Disorders Research (11 papers) and Diet and metabolism studies (10 papers). The work is most often cited by research in Clinical Biochemistry (575 citations), Biochemistry (146 citations), Cell Biology (254 citations), Rheumatology (184 citations) and Physiology (249 citations). Ayşegül Tokatlı has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Turgay Coşkun, İ Özalp, Ali Dursun, Hatice Serap Sivri, Yılmaz Yıldız, Rıza Köksal Özgül, H. Serap Kalkanoğlu, Haluk Topaloğlu, Serap Sivri and Beril Talim. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Journal of Child Neurology, The Journal of Pediatrics and European Journal of Medical Genetics.
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.