OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
- Journal
- Nature Genetics
In The Last Decade
doi.org/10.1038/79944 →Countries where authors are citing OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
This map shows the geographic impact of OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. 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 OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 more than expected).
Fields of papers citing OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
This network shows the impact of OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
About OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
This paper, published in 2000, received 1.0k indexed citations . Written by Christiane Alexander, Marcela Votruba, Dawn L. Thiselton, Simone Mayer, Anthony T. Moore, Miguel Rodríguez, Ulrich Kellner, Beate Leo‐Kottler, Georg Auburger and Bernd Wissinger covering the research area of Molecular Biology and Cell Biology. It is primarily cited by scholars working on Molecular Biology (969 citations), Clinical Biochemistry (341 citations) and Cellular and Molecular Neuroscience (136 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/10.1038/79944.