Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder.
Abstract
loading...
About
In The Last Decade
doi.org/w80327896 →Countries where authors are citing Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder.
This map shows the geographic impact of Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder.. 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 Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder. with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder. more than expected).
Fields of papers citing Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder.
This network shows the impact of Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder.. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder..
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/w80327896.