ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43

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This paper, published in 1950, received 494 indexed citations. Written by Radu Stoica, Kurt J. De Vos, Sébastien Paillusson, Sarah B. Mueller, Rosa M. Sancho, Kwok‐Fai Lau, Gema Vizcay‐Barrena, Wen-Lang Lin, Ya-Fei Xu and Jada Lewis covering the research area of Neurology, Molecular Biology and Cell Biology. It is primarily cited by scholars working on Molecular Biology (381 citations), Cell Biology (173 citations) and Neurology (153 citations). Published in Nature Communications.

Countries where authors are citing ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43

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This map shows the geographic impact of ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43. 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 ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43 with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43 more than expected).

Fields of papers citing ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43

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Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43.

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This paper is also available at doi.org/10.1038/ncomms4996.

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