Recherche
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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 -
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 -
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
(Communications Biology. vol. 5, n° 1, 2022-04-08)Article de revueLibre accès -
International stroke genetics consortium recommendations for studies of genetics of stroke outcome and recovery
(International Journal of Stroke. vol. 17, n° 3, pp. 260-268, 2022-03-01)Article de revueLibre accès -
Stroke Genetics: Discovery, Insight Into Mechanisms, and Clinical Perspectives
(Circulation Research. vol. 130, n° 8, pp. 1095-1111, 2022-04-15)Article de revue -
Editorial: Population Neuroscience of Development and Aging
(Frontiers in Systems Neuroscience. vol. 16, pp. 897943, 2022-04-25)Article de revueLibre accès -
Cervical Artery Dissection and Sports
(Frontiers in Neurology. vol. 12, pp. 663830, 2021-05-31)Article de revueLibre accès