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Cerebral small vessel disease genomics and its implications across the lifespan
Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities
Genetic architecture of subcortical brain structures in 38,851 individuals
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes
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
Novel genetic loci underlying human intracranial volume identified through genome-wide association