Petr Chrastina
- Co-authors
- Tomáš AdamKarolína PeškováJ ZemanJakub KrijtViktor KožichHana HansíkováLászló WenchichStanislav Kmoch
- Topics
- Metabolism and Genetic Disorders (15 papers)Neonatal Health and Biochemistry (5 papers)Mitochondrial Function and Pathology (4 papers)
In The Last Decade
Petr Chrastina
17 papers receiving 250 citations
Peers
Comparison fields: 5 of 59
- Molecular Biology 134
- Clinical Biochemistry 106
- Physiology 72
- Biochemistry 36
- Rheumatology 33
Countries citing papers authored by Petr Chrastina
This map shows the geographic impact of Petr Chrastina'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 Petr Chrastina with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Petr Chrastina more than expected).
Fields of papers citing papers by Petr Chrastina
This network shows the impact of papers produced by Petr Chrastina. 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 Petr Chrastina. The network helps show where Petr Chrastina may publish in the future.
Co-authorship network of co-authors of Petr Chrastina
This figure shows the co-authorship network connecting the top 25 collaborators of Petr Chrastina. A scholar is included among the top collaborators of Petr Chrastina 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 Petr Chrastina. Petr Chrastina is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 4 | |
| 3 | 1 | |
| 4 | 6 | |
| 5 | 4 | |
| 6 | X-linked adrenoleukodystrophy: phenotype-genotype correlation in hemizygous males and heterozygous females with ABCD1 mutations. | 4 |
| 7 | 15 | |
| 8 | 6 | |
| 9 | 30 | |
| 10 | 17 | |
| 11 | [Clinical, biochemical and molecular characteristics in 11 Czech children with tyrosinemia type I]. | 4 |
| 12 | 60 | |
| 13 | 1 | |
| 14 | 54 | |
| 15 | 12 | |
| 16 | Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency. | 24 |
| 17 | 13 |
About Petr Chrastina
Petr Chrastina is a scholar working on Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Physiology, having authored 17 papers that have together received 256 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (15 papers), Neonatal Health and Biochemistry (5 papers) and Mitochondrial Function and Pathology (4 papers). The work is most often cited by research in Clinical Biochemistry (106 citations), Biochemistry (36 citations) and Physiology (72 citations). Petr Chrastina has collaborated with scholars based in Czechia, Serbia and Australia. Frequent co-authors include Tomáš Adam, Karolína Pešková, J Zeman, Jakub Krijt, Viktor Kožich, Hana Hansíková, László Wenchich, Stanislav Kmoch, K. Harzer and Barbara C. Paton. Their work appears in journals such as Nutrients, Clinica Chimica Acta and Acta Paediatrica.
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.