Hadil Kathom
Impact in
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- Metabolism and Genetic Disorders
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- Amino Acid Enzymes and Metabolism
Papers in
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- Mitochondrial Function and Pathology 2
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- Metabolism and Genetic Disorders 2
- Co-authors
- Radka Tincheva (2 shared papers)Iglika Yordanova (1 shared paper)Ivan Litvinenko (1 shared paper)Teodora Chamova (1 shared paper)Velina Guergueltcheva (1 shared paper)Bilyana Georgieva (1 shared paper)Ivailo Tournev (1 shared paper)Tihomir Todorov (1 shared paper)
- Journals
- Journal of Genetics (1 paper)PubMed (2 papers)
- Partner nations
- Bulgaria
In The Last Decade
Hadil Kathom
3 papers receiving 23 citations
Peers
Comparison fields: 5 of 12
- Clinical Biochemistry 14
- Biochemistry 3
- Pediatrics, Perinatology and Child Health 6
- Physiology 1
- Molecular Biology 13
Countries citing papers authored by Hadil Kathom
This map shows the geographic impact of Hadil Kathom'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 Hadil Kathom with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hadil Kathom more than expected).
Fields of papers citing papers by Hadil Kathom
This network shows the impact of papers produced by Hadil Kathom. 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 Hadil Kathom. The network helps show where Hadil Kathom may publish in the future.
Co-authors
The 10 scholars most cited alongside Hadil Kathom, 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 | First Bulgarian case of citrin deficiency caused by one novel and one recurrent mutation in the SLC25A13 gene. | 2014 | 11 |
| 2 | BARTH SYNDROME IN MALE AND FEMALE SIBLINGS CAUSED BY A NOVEL MUTATION IN THE TAZ GENE. | 2018 | 11 |
| 3 | 2022 | 1 |
About Hadil Kathom
Hadil Kathom is a scholar working on Molecular Biology, Clinical Biochemistry, Cardiology and Cardiovascular Medicine, Pediatrics, Perinatology and Child Health and Physiology, having authored 3 papers that have together received 23 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (2 papers), Mitochondrial Function and Pathology (2 papers), Neonatal Health and Biochemistry (1 paper), Cardiomyopathy and Myosin Studies (1 paper), Cardiovascular Effects of Exercise (1 paper), Amino Acid Enzymes and Metabolism (1 paper) and Diet and metabolism studies (1 paper). The work is most often cited by research in Clinical Biochemistry (14 citations), Biochemistry (3 citations), Pediatrics, Perinatology and Child Health (6 citations), Physiology (1 citation) and Molecular Biology (13 citations). Hadil Kathom has collaborated with scholars based in Bulgaria. Frequent co-authors include Radka Tincheva, Iglika Yordanova, Ivan Litvinenko, Teodora Chamova, Velina Guergueltcheva, Bilyana Georgieva, Ivailo Tournev, Tihomir Todorov, Alexey Savov and Албена Тодорова. Their work appears in journals such as Journal of Genetics and PubMed.
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.