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Plasma trimethylamine N-oxide (TMAO)
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Longitudinal brain atrophy rates in presymptomatic carriers of genetic frontotemporal dementia
Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia
Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia
Pericardial adipose tissue, cardiac structures, and cardiovascular risk factors in school-age children
Association of common genetic variants with brain microbleeds
Cerebral small vessel disease genomics and its implications across the lifespan
Ethnic differences in childhood right and left cardiac structure and function assessed by cardiac magnetic resonance imaging
Circulating metabolites are associated with brain atrophy and white matter hyperintensities
Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities
Genetic architecture of subcortical brain structures in 38,851 individuals
Hemoglobin and anemia in relation to dementia risk and accompanying changes on brain MRI
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes
Development and Validation of a Dementia Risk Prediction Model in the General Population: An Analysis of Three Longitudinal Studies
Detection of mild cognitive impairment in a community-dwelling population using quantitative, multiparametric MRI-based classification
Detection of mild cognitive impairment in a community-dwelling population using quantitative, multiparametric MRI-based classification
Patterns of functional connectivity in an aging population: The Rotterdam Study
Patterns of functional connectivity in an aging population: The Rotterdam Study
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging
Clinical significance of cerebral microbleeds on MRI: A comprehensive meta-analysis of risk of intracerebral hemorrhage, ischemic stroke, mortality, and dementia in cohort studies (v1)
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms
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