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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
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Operational tolerance after hematopoietic stem cell transplantation is characterized by distinct transcriptional, phenotypic, and metabolic signatures
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MYT1L-associated neurodevelopmental disorder : description of 40 new cases and literature review of clinical and molecular aspects
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Monocyte transcriptomes from patients with axial spondyloarthritis reveal dysregulated monocytopoiesis and a distinct inflammatory imprint
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Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
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Where are the missing gene defects in inherited retinal disorders? : intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
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Analysis of shared heritability in common disorders of the brain
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Bivariate association analysis in selected samples : application to a GWAS of two bone mineral density phenotypes in males with high or low BMD
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Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine