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Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.
(Brain - A Journal of Neurology, 2022-05-02)Article de revue -
Burden of Dilated Perivascular Spaces, an Emerging Marker of Cerebral Small Vessel Disease, Is Highly Heritable
(Stroke. vol. 49, n° 2, pp. 282-287, 2018-02)Article de revue -
Genetic architecture of subcortical brain structures in 38,851 individuals
(Nature Genetics. vol. 51, n° 11, pp. 1624-1636, 2019-11)Article de revue -
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(Nature Genetics. vol. 50, n° 10, pp. 1412-1425, 2018-10)Article de revue -
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 -
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 -
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 -
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 -
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 -
Correction: The genetic history of France
(European Journal of Human Genetics. vol. 28, n° 7, pp. 988, 2020)Article de revue