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UnknownRare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
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S-EPMC4189898 | biostudies-literature
UnknownIdentification of a rare coding variant in complement 3 associated with age-related macular degeneration.
Not available
S-EPMC3812337 | biostudies-literature
UnknownA novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Not available
S-EPMC3303079 | biostudies-literature
UnknownA large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Not available
S-EPMC4745342 | biostudies-literature
UnknownRare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Not available
S-EPMC9653013 | biostudies-literature
UnknownEffects of icosapent ethyl according to baseline residual risk in patients with atherosclerotic cardiovascular disease: results from REDUCE-IT.
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S-EPMC11873788 | biostudies-literature
UnknownConvalescent plasma in patients admitted to hospital with COVID-19 (RECOVERY): a randomised controlled, open-label, platform trial.
Not available
S-EPMC8121538 | biostudies-literature
UnknownBaricitinib in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial and updated meta-analysis.
Not available
S-EPMC9333998 | biostudies-literature
UnknownCasirivimab and imdevimab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC8830904 | biostudies-literature
UnknownEmpagliflozin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC10957483 | biostudies-literature
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