Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma
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doi.org/10.1038/ng.2523 →Countries where authors are citing Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma
This map shows the geographic impact of Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma. 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 Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma more than expected).
Fields of papers citing Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma
This network shows the impact of Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma.
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.
This paper is also available at doi.org/10.1038/ng.2523.