Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars
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doi.org/10.1038/nbt.4124 →Countries where authors are citing Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars
This map shows the geographic impact of Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars. 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 Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars more than expected).
Fields of papers citing Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars
This network shows the impact of Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the Simultaneous lineage tracing and cell-type identification using CRISPR–Cas9-induced genetic scars.
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/nbt.4124.