Division of Clinical and Metabolic Genetics, SickKids U of T
Canada
1 December 2019 - 30 November 2020
Principal institution: The Hospital for Sick Children (SickKids), U of T
Region: Global
Subject/journal group: All
The table to the right includes counts of all research outputs for Division of Clinical and Metabolic Genetics, SickKids U of T 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.
| Count | Share |
|---|---|
| 5 | 0.15 |
Outputs by subject (Share)
| Subject | Count | Share | |
|---|---|---|---|
| Life Sciences | 5 | 0.15 | |
Top articles by Altmetric score in current window
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes.
American Journal of Human Genetics
2020-03-31
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism.
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
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas.
American Journal of Human Genetics
2020-06-04
Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations.
American Journal of Human Genetics
2019-12-16
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