Associated Papers
Common protein-altering variant in GFAP is associated with white matter lesions in the older Japanese population.
Furuta Y et al.
Npj Genomic Medicine, 2024
White matter hyperintensity genetic risk factor TRIM47 regulates autophagy in brain endothelial cells.
Yeung SH et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2024
White matter hyperintensity genetic risk factor TRIM47 regulates autophagy in brain endothelial cells.
Yeung SH et al.
Biorxiv : the Preprint Server for Biology, 2024
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.
Mishra A et al.
Brain : a Journal of Neurology, 2022
Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants.
Persyn E et al.
Nature Communications, 2020
Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226).
Traylor M et al.
Neurology, 2019
The Associations of PMF1, ICAM1, AGT, TRIM65, FBF1, and ACOX1 Variants With Leukoaraiosis in Chinese Population.
Huang WQ et al.
Frontiers in Genetics, 2019
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.
Verhaaren BF et al.
Circulation. Cardiovascular Genetics, 2015
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