Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
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- Nature Genetics
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doi.org/10.1038/1252 →Countries where authors are citing Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
This map shows the geographic impact of Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B. 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 Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B more than expected).
Fields of papers citing Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
This network shows the impact of Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B.
About Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
This paper, published in 1998, received 783 indexed citations . Written by Robyn H. Wallace, Dao Wen Wang, Rita Singh, Ingrid E. Scheffer, Alfred L. George, Hilary A. Phillips, Kathrin Saar, André Reis, Eric W. Johnson and Grant R. Sutherland covering the research area of Molecular Biology, Cellular and Molecular Neuroscience and Psychiatry and Mental health. It is primarily cited by scholars working on Molecular Biology (487 citations), Psychiatry and Mental health (442 citations) and Cellular and Molecular Neuroscience (428 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/10.1038/1252.