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Genetics of common cerebral small vessel disease
(Nature Reviews Neurology. vol. 18, n° 2, pp. 84-101, 2022-01-05)Article de revueLibre accès -
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease
(JAMA neurology, 2022-05-31)Article de revue -
Heritable and non-heritable uncommon causes of stroke
(Journal of Neurology. vol. 268, n° 8, pp. 2780-2807, 2021-08)Article de revue -
Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse
(Circulation-Genomic and Precision Medicine. vol. 14, n° 5, pp. CIRCGEN120003148, 2021-08-31)Article de revue -
Genome-wide association study identifies first locus associated with susceptibility to cerebral venous thrombosis
(Annals of Neurology, 2021-08-30)Article de revue -
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
(Nature Communications. vol. 13, n° 1, 2022-08-03)Article de revueLibre accès -
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
(Molecular Psychiatry, 2022-08-16)Article de revueLibre accès -
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI
(Brain - A Journal of Neurology, 2022-08-09)Article de revueLibre accès -
Stroke-associated intergenic variants modulate a human FOXF2 transcriptional enhancer
(Proceedings of the National Academy of Sciences of the United States of America. vol. 119, n° 35, 2022-08-30)Article de revueLibre accès -
How has the future investment program stimulated research and innovation in health?
(Therapies. vol. 77, n° 1, pp. 19-24, 2022-01-01)Article de revue