1 December 2019 - 30 November 2020
Principal institution: Université du Québec à Montréal (UQAM)
Subject/journal group: All
The table to the right includes counts of all research outputs for Center of Excellence in Research on Orphan Diseases – Fondation Courtois (CERMO-FC), UQAM published between 1 December 2019 - 30 November 2020 which are tracked by the Nature Index.
Hover over the donut graph to view the FC output for each subject. Below, the same research outputs are grouped by subject. Click on the subject to drill-down into a list of articles organized by journal, and then by title.
Note: Articles may be assigned to more than one subject area.
Outputs by subject (Share)
|Proceedings of the National Academy of Sciences of the United States of America||1||0.01|
Top articles by Altmetric score in current window
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Proceedings of the National Academy of Sciences of the United States of America
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