Service de Génétique Médicale, CHU de Nantes
France
1 July 2019 - 30 June 2020
Principal institution: University Hospital Nantes (CHU de Nantes)
Region: Global
Subject/journal group: All
The table to the right includes counts of all research outputs for Service de Génétique Médicale, CHU de Nantes published between 1 July 2019 - 30 June 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 |
|---|---|
| 6 | 0.32 |
Outputs by subject (Share)
| Subject | Count | Share | |
|---|---|---|---|
| Life Sciences | 6 | 0.32 | |
Top articles by Altmetric score in current window
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
American Journal of Human Genetics
2019-05-09
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.
American Journal of Human Genetics
2019-02-28
RPL13 Variants Cause Spondyloepimetaphyseal Dysplasia with Severe Short Stature.
American Journal of Human Genetics
2019-10-14
Complex Compound Inheritance of Lethal Lung Developmental Disorders due to Disruption of the TBX-FGF Pathway.
American Journal of Human Genetics
2019-01-02
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