Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium

670 indexed citations
published 2008

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This map shows the geographic impact of Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium. 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 Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium more than expected).

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Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium.

About Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium

This paper, published in 2008, received 670 indexed citations . Written by Emyr Lloyd‐Evans, Anthony J. Morgan, Xingxuan He, David A. Smith, Daniel J. Sillence, Grant C. Churchill, Edward H. Schuchman and Frances M. Platt covering the research area of Molecular Biology, Physiology and Physiology. It is primarily cited by scholars working on Physiology (340 citations), Physiology (298 citations), Molecular Biology (243 citations), Cell Biology (219 citations) and Epidemiology (122 citations). Published in Nature Medicine.

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/nm.1876.

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