Vlad Makarov
- Co-authors
- Iuliana Ionita‐LazaJoseph D. BuxbaumXihong LinSeunggeun LeeBin XuJoseph A. GogosMaria KarayiorgouJohannes L. Roos
- Topics
- Genomics and Rare Diseases (4 papers)Genomic variations and chromosomal abnormalities (4 papers)Genetic Associations and Epidemiology (3 papers)
- Journals
- Proceedings of the National Academy of SciencesCancer ResearchThe American Journal of Human Genetics
- Partner nations
- United States
In The Last Decade
Vlad Makarov
5 papers receiving 418 citations
Peers
Comparison fields: 5 of 63
- Genetics 293
- Molecular Biology 207
- Epidemiology 26
- Cognitive Neuroscience 22
- Physiology 22
Countries citing papers authored by Vlad Makarov
This map shows the geographic impact of Vlad Makarov'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 Vlad Makarov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vlad Makarov more than expected).
Fields of papers citing papers by Vlad Makarov
This network shows the impact of papers produced by Vlad Makarov. 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 Vlad Makarov. The network helps show where Vlad Makarov may publish in the future.
Co-authorship network of co-authors of Vlad Makarov
This figure shows the co-authorship network connecting the top 25 collaborators of Vlad Makarov. A scholar is included among the top collaborators of Vlad Makarov 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 Vlad Makarov. Vlad Makarov 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 | 285 | |
| 3 | 56 | |
| 4 | 41 | |
| 5 | 37 |
About Vlad Makarov
Vlad Makarov is a scholar working on Genetics, Cancer Research and Radiology, Nuclear Medicine and Imaging, having authored 5 papers that have together received 420 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Associations and Epidemiology (3 papers). The work is most often cited by research in Genetics (293 citations), Molecular Biology (207 citations) and Statistics and Probability (12 citations). Vlad Makarov has collaborated with scholars based in United States. Frequent co-authors include Iuliana Ionita‐Laza, Joseph D. Buxbaum, Xihong Lin, Seunggeun Lee, Bin Xu, Joseph A. Gogos, Maria Karayiorgou, Johannes L. Roos, Benjamin A. Raby and Seungtai Yoon. Their work appears in journals such as Proceedings of the National Academy of Sciences, Cancer Research and The American Journal of Human 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.