How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models

Paige Hall, Michael Wangler, Jonathan Andrews

Open source

DOI
10.1146/annurev-genom-020525-025811
Published
2026-08-25
Container
Annual Review of Genomics and Human Genetics
Publisher
Annual Reviews
Open access
unknown

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BibTeX

@article{allodium:10.1146/annurev-genom-020525-025811,
  title = {How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models},
  author = {Paige Hall and Michael Wangler and Jonathan Andrews},
  year = {2026},
  journal = {Annual Review of Genomics and Human Genetics},
  doi = {10.1146/annurev-genom-020525-025811},
  url = {https://doi.org/10.1146/annurev-genom-020525-025811}
}

RIS

TY  - JOUR
TI  - How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models
AU  - Paige Hall
AU  - Michael Wangler
AU  - Jonathan Andrews
PY  - 2026
JO  - Annual Review of Genomics and Human Genetics
DO  - 10.1146/annurev-genom-020525-025811
UR  - https://doi.org/10.1146/annurev-genom-020525-025811
ER  - 

APA

Hall, P., Wangler, M., & Andrews, J. (2026). How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models. Annual Review of Genomics and Human Genetics. https://doi.org/10.1146/annurev-genom-020525-025811

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