Associated Papers
Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammation.
Neumann A et al.
Molecular Psychiatry, 2022
35173266 (PubMed )
Supplement: 41380_2022_1437_MOESM2_ESM.xlsx › single_variants_annotation
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits.
Unknown Author
Nature Genetics, 2016
27399967 (PubMed )
Supplement: NIHMS793138-supplement-Suppl_tables.xlsx › S9a
Select a paper to view details