Genetic associations between ULK3 and epilepsy: a two-sample Mendelian randomization study
This study suggests a causal relationship between ULK3 and the risk of focal epilepsy from a genetic perspective. Nevertheless, further investigation is needed to understand the role of ULK3 in epilepsy fully.
Authors
- B.-H. Liu
- Keyi Fan (ORCID: https://orcid.org/0000-0002-1820-9107)
- Zhihao Su (ORCID: https://orcid.org/0000-0002-6972-1848)
- Heyi Zhang (ORCID: https://orcid.org/0000-0003-0443-3367)
- Sheng‐Xiao Zhang (ORCID: https://orcid.org/0000-0003-1341-7588)
- Zhentong Liu
- Shuhan Xu
- Shangkai Bai
- Huiting Cao
- Xinyi Zheng
- Yaochen Zhang
Institutions
- Shanxi Medical University (CN)
Publication Details
- Journal
- Frontiers in Neurology
- Published
- 2024-08-12
- DOI
- https://doi.org/10.3389/fneur.2024.1376314
- Citations
- 1
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.55