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Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosis.
Not available
S-EPMC11036449
|
biostudies-literature
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Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
Not available
S-EPMC3084597
|
biostudies-literature
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Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification.
Not available
S-EPMC11138106
|
biostudies-literature
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The Association of Prenatal Dietary Factors with Child Autism Diagnosis and Autism-Related Traits Using a Mixtures Approach: Results from the Environmental Influences on Child Health Outcomes Cohort.
Not available
S-EPMC12264552
|
biostudies-literature
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Relationship Between Preexisting Cardiovascular Disease and Death and Cardiovascular Outcomes in Critically Ill Patients With COVID-19.
Not available
S-EPMC9575399
|
biostudies-literature
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100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
Not available
S-EPMC7613219
|
biostudies-literature
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HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.
Not available
S-EPMC4702958
|
biostudies-literature
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CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion.
Not available
S-EPMC3306163
|
biostudies-literature
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Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Not available
S-EPMC10932913
|
biostudies-literature
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