Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
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- Nature Genetics
In The Last Decade
doi.org/10.1038/6799 →Countries where authors are citing Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
This map shows the geographic impact of Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. 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 Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy more than expected).
Fields of papers citing Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
This network shows the impact of Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
About Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
This paper, published in 1999, received 1.0k indexed citations . Written by Gisèle Bonne, Marina Raffaele di Barletta, Shaïda Varnous, Henri-Marc Bécane, E. Hammouda, Luciano Merlini, Francesco Muntoni, Cheryl R. Greenberg, Françoise Gary and J.A. Urtizberea covering the research area of Molecular Biology. It is primarily cited by scholars working on Molecular Biology (965 citations), Cardiology and Cardiovascular Medicine (191 citations) and Cell Biology (139 citations). Published in Nature 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.
This paper is also available at doi.org/10.1038/6799.