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UnknownGenomic structural equation modeling reveals latent phenotypes in the human cortex with distinct genetic architecture.
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S-EPMC11502831 | biostudies-literature
UnknownSpatial and Functional Distribution of <i>MYBPC3</i> Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy.
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S-EPMC7676622 | biostudies-literature
UnknownTowards cascading genetic risk in Alzheimer's disease.
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S-EPMC11292901 | biostudies-literature
UnknownEnhancing cognitive performance prediction by white matter hyperintensity connectivity assessment.
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S-EPMC11629703 | biostudies-literature
UnknownBiallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
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S-EPMC6117612 | biostudies-literature
UnknownA toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.
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S-EPMC7385984 | biostudies-literature
UnknownHNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.
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S-EPMC10432175 | biostudies-literature
UnknownA multi-country analysis of COVID-19 hospitalizations by vaccination status.
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S-EPMC10935543 | biostudies-literature
Unknown10-year stroke prevention after successful carotid endarterectomy for asymptomatic stenosis (ACST-1): a multicentre randomised trial.
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S-EPMC2956884 | biostudies-literature
UnknownBiallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
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S-EPMC10932913 | biostudies-literature
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