Centre for Rare Diseases (ZSE), Uni Tübingen
Germany
1 November 2019 - 31 October 2020
Principal institution: University Hospital Tübingen (UKT), Uni Tübingen
Region: Global
Subject/journal group: All
The table to the right includes counts of all research outputs for Centre for Rare Diseases (ZSE), Uni Tübingen published between 1 November 2019 - 31 October 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.
Count | Share |
---|---|
2 | 0.03 |
Outputs by subject (Share)
Subject | Count | Share | |
---|---|---|---|
Life Sciences | 2 | 0.03 |
Top articles by Altmetric score in current window
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.
American Journal of Human Genetics
2020-08-06
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects.
American Journal of Human Genetics
2020-08-06

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