Investigating the sources of variable impact of pathogenic variants in monogenic metabolic conditions
Abstract Over three percent of people carry a dominant pathogenic variant, yet only a fraction of carriers develop disease. Disease phenotypes from carriers of variants in the same gene range from mild to severe. Here, we investigate underlying mechanisms for this heterogeneity: variable variant eff...
Saved in:
| Main Authors: | Angela Wei, Richard Border, Boyang Fu, Sinéad Cullina, Nadav Brandes, Seon-Kyeong Jang, Sriram Sankararaman, Eimear E. Kenny, Miriam S. Udler, Vasilis Ntranos, Noah Zaitlen, Valerie A. Arboleda |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-06-01
|
| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-025-60339-7 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney Disease
by: Laura R. Claus, et al.
Published: (2024-09-01) -
Genetic variants explain ancestry‐related differences in type 2 diabetes risk
by: Aaron J. Deutsch, et al.
Published: (2024-11-01) -
Genetic Variants in Early-Onset Inflammatory Bowel Disease: Monogenic Causes and Clinical Implications
by: Duygu Demirtas Guner, et al.
Published: (2025-04-01) -
Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance
by: Reema Alduaiji, et al.
Published: (2023-02-01) -
Clinical approach to monogenic Parkinson’s disease
by: Manu S. Girija, et al.
Published: (2025-01-01)