Hadil Kathom

702 total citations
3 papers, 23 citations indexed

About

Hadil Kathom is a scholar working on Molecular Biology, Clinical Biochemistry and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Hadil Kathom has authored 3 papers receiving a total of 23 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Clinical Biochemistry and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Hadil Kathom's work include Metabolism and Genetic Disorders (2 papers), Mitochondrial Function and Pathology (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Hadil Kathom is often cited by papers focused on Metabolism and Genetic Disorders (2 papers), Mitochondrial Function and Pathology (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Hadil Kathom collaborates with scholars based in Bulgaria. Hadil Kathom's co-authors include M. Ivanova, Radka Tincheva, Ivan Litvinenko, Iglika Yordanova, Ivailo Tournev, Албена Тодорова, Teodora Chamova, Tihomir Todorov, Bilyana Georgieva and Velina Guergueltcheva and has published in prestigious journals such as Journal of Genetics and PubMed.

In The Last Decade

Hadil Kathom

3 papers receiving 23 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hadil Kathom Bulgaria	2	15	14	7	5	5	3	23
Inmaculada González-Gallego Spain	2	19 1.3×	5 0.4×	10 1.4×	2 0.4×	6 1.2×	2	25
Nebal Waill Saadi Iraq	3	13 0.9×	13 0.9×	6 0.9×		5 1.0×	6	25
Jaime Barea United States	2	8 0.5×	6 0.4×	3 0.4×	1 0.2×	6 1.2×	3	21
J. Hunt United States	2	24 1.6×	13 0.9×	9 1.3×		2 0.4×	3	30
Mohammed M. Saleh Saudi Arabia	3	11 0.7×	17 1.2×	3 0.4×	1 0.2×	12 2.4×	4	28
Alma Sikiric Norway	2	11 0.7×	10 0.7×	3 0.4×		1 0.2×	3	17
Т. П. Бардымова Russia	3	3 0.2×	5 0.4×	5 0.7×	3 0.6×	8 1.6×	13	29
Neil Lawrence United Kingdom	4	8 0.5×	21 1.5×		7 1.4×	3 0.6×	11	35
Anna Chassevent United States	2	3 0.2×	23 1.6×	2 0.3×	3 0.6×	7 1.4×	2	27
Nandini Avula United States	3	2 0.1×	14 1.0×	9 1.3×	5 1.0×	2 0.4×	6	27

Countries citing papers authored by Hadil Kathom

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Hadil Kathom

This figure shows the co-authorship network connecting the top 25 collaborators of Hadil Kathom. A scholar is included among the top collaborators of Hadil Kathom 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 Hadil Kathom. Hadil Kathom is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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3 of 3 papers shown

1.

Todorov, Tihomir, M. Ivanova, Teodora Chamova, et al.. (2022). Arginase deficiency in Bulgaria: first cases and potential endemic region for the disorder. Journal of Genetics. 102(1). 1 indexed citations

2.

Kathom, Hadil, et al.. (2018). BARTH SYNDROME IN MALE AND FEMALE SIBLINGS CAUSED BY A NOVEL MUTATION IN THE TAZ GENE.. PubMed. 27(4). 495–501. 11 indexed citations

3.

Ivanova, M., et al.. (2014). First Bulgarian case of citrin deficiency caused by one novel and one recurrent mutation in the SLC25A13 gene.. PubMed. 25(3). 271–6. 11 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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