Institute of Human Genetics, HHU
Institut für Humangenetik, HHU
Germany
1 April 2019 - 31 March 2020
Principal institution: University Hospital Duesseldorf (UKD)
Region: Global
Subject/journal group: All
The table to the right includes counts of all research outputs for Institute of Human Genetics, HHU published between 1 April 2019 - 31 March 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 |
|---|---|
| 4 | 0.45 |
Outputs by subject (Share)
| Subject | Count | Share | |
|---|---|---|---|
| Life Sciences | 4 | 0.45 | |
Top articles by Altmetric score in current window
Mutations in and in other Coffin–Siris syndrome genes lead to various brain midline defects
Nature Communications
2019-07-04
Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly.
American Journal of Human Genetics
2019-09-17
Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities.
American Journal of Human Genetics
2020-01-25
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