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Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
(Stroke. vol. 51, n° 7, pp. 2111-2121, 2020)Article de revue -
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants
(Alzheimer's and Dementia, 2021-05-18)Article de revueLibre acceso -
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
(Nature genetics. vol. 51, n° 7, pp. 1192-1193, 2019-07)Article de revue -
Correction: The genetic history of France
(European Journal of Human Genetics. vol. 28, n° 7, pp. 988, 2020)Article de revue -
Fish Intake, Genetic Predisposition to Alzheimer Disease, and Decline in Global Cognition and Memory in 5 Cohorts of Older Persons
(American journal of epidemiology. vol. 187, n° 5, pp. 933-940, 2018-05-01)Article de revue -
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
(Nature Genetics. vol. 50, n° 4, pp. 524-537, 2018-03-12)Article de revue -
Impact of interventions scenarios targeting three main vascular risk factors on the future burden of dementia in France
(European Journal of Epidemiology, 2023-02-28)Article de revueLibre acceso -
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy
(Movement Disorders. vol. 34, n° 7, pp. 1049-1059, 2019)Article de revue -
The genetic history of France
(European Journal of Human Genetics. vol. 28, n° 7, pp. 853-865, 2020)Article de revue -
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(Nature Genetics. vol. 50, n° 12, pp. 1755, 2018-12)Article de revue