Summary statistics are available for download from the Kiryluk lab website.
Publications
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.
Xie J, Liu L, Mladkova M, et al.
Nat Commun. 2020 Mar 30;11(1):1600. doi: 10.1038/s41467-020-15383-w.
PMID:32231244
Phenotypes
- Membranous nephropathy
Experiment summary
This study is an analysis of genetic associations for membranous nephropathy (MN), a rare autoimmune disorder that leads to nephrotic syndrome and kidney failure, in 3,782 MN cases and 9,038 ancestry-matched controls. This dataset is a trans-ethnic meta-analysis across participants of East Asian and European ancestries. Single-ancestry datasets are also available in the Portal:
Dataset ID
Xie2020_MemNeph_mixed