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- Journal Article
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- open access
Shared heritability and functional enrichment across six solid cancers
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- Journal Article
- A1
- open access
Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia
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Familial aggregation of pure tone hearing thresholds in an aging European population
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Genetic signature of population fragmentation varies with mobility in seven bird species of a fragmented Kenyan cloud forest
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Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami