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
Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis.
Skarp S et al.
Plos One, 2018
30157244 (PubMed )
Supplement: pone.0203313.s001.xlsx › Family8_SNPs
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
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