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UnknownGenome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
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S-EPMC4469997 | biostudies-literature
UnknownGenetic 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.
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S-EPMC11036449 | biostudies-literature
UnknownMeta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
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S-EPMC3084597 | biostudies-literature
UnknownGenomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
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S-EPMC7614484 | biostudies-literature
UnknownTowards cascading genetic risk in Alzheimer's disease.
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S-EPMC11292901 | biostudies-literature
UnknownMutual learning for joint disease detection and severity prediction reveals multimodal pathogenesis for neurodegenerative disorders.
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S-EPMC12758602 | biostudies-literature
UnknownNeuropsychiatric symptoms in cognitive decline and Alzheimer's disease: biomarker discovery using plasma proteomics.
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S-EPMC12015082 | biostudies-literature
UnknownEnhancing cognitive performance prediction by white matter hyperintensity connectivity assessment.
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S-EPMC11629703 | biostudies-literature
UnknownDeep learning enhanced ALPS reveals genetic and environmental factors of brain glymphatic function.
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S-EPMC12878677 | biostudies-literature
UnknownThe genetic architecture of the human cerebral cortex.
Not available
S-EPMC7295264 | biostudies-literature
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