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UnknownDiagnostic Accuracy Prior to Congenital Heart Defect Surgery: A Multicenter Collaboration.
Not available
S-EPMC11905157 | biostudies-literature
UnknownA deep catalog of protein-coding variation in 985,830 individuals.
Not available
S-EPMC10197621 | biostudies-literature
UnknownRare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries.
Not available
S-EPMC12932796 | biostudies-literature
UnknownExclusion-based exome sequencing in critically ill adults 18-40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing.
Not available
S-EPMC12414659 | biostudies-literature
UnknownMulti-ethnic heterozygote frequencies of cancer susceptibility genes to inform counseling of reproductive risk.
Not available
S-EPMC11717631 | biostudies-literature
UnknownRisk of lymphoid malignancy associated with cancer predisposition genes.
Not available
S-EPMC12009404 | biostudies-literature
UnknownPMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients.
Not available
S-EPMC11613782 | biostudies-literature
UnknownA large meta-analysis identifies genes associated with anterior uveitis.
Not available
S-EPMC10638276 | biostudies-literature
UnknownGenome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease.
Not available
S-EPMC9005345 | biostudies-literature
UnknownRare coding variants in CHRNB2 reduce the likelihood of smoking.
Not available
S-EPMC10335934 | biostudies-literature
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