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Estimated prevalence, tumor spectrum, and neurofibromatosis type 1-like phenotype of CDKN2A-related melanoma-astrocytoma syndrome
The genomics of heart failure
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function
Rare and low-frequency coding variants alter human adult height