5 papers found
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosisDownload from doi.org
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaDownload from doi.org
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran ProgramDownload from doi.org
Rare variants in SLC5A10 are associated with serum 1,5-anhydroglucitol (1,5-AG) in the Atherosclerosis Risk in Communities (ARIC) StudyDownload from doi.org
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levelsDownload from doi.org
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