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UnknownWhole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals.
Not available
S-EPMC12418676 | biostudies-literature
UnknownVariants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain.
Not available
S-EPMC8354857 | biostudies-literature
UnknownGenetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium.
Not available
S-EPMC8059115 | biostudies-literature
UnknownRare variant contribution to the heritability of coronary artery disease.
Not available
S-EPMC11464707 | biostudies-literature
UnknownStereoacuity in children with anisometropic amblyopia.
Not available
S-EPMC3223370 | biostudies-literature
UnknownDeep-coverage whole genome sequences and blood lipids among 16,324 individuals.
Not available
S-EPMC6107638 | biostudies-literature
UnknownWhole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma.
Not available
S-EPMC6904857 | biostudies-literature
UnknownDeep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Not available
S-EPMC6031652 | biostudies-literature
UnknownChromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.
Not available
S-EPMC8042019 | biostudies-literature
UnknownGenome sequencing unveils a regulatory landscape of platelet reactivity.
Not available
S-EPMC8206369 | biostudies-literature
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