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Anzahl der Publikationen: 4
Zeitschriftenartikel
Traylor, Matthew; Anderson, Christopher D.; Rutten-Jacobs, Loes C. A.; Falcone, Guido J.; Comeau, Mary E.; Ay, Hakan; Sudlow, Cathie L. M.; Xu, Huichun; Mitchell, Braxton D.; Cole, John W.; Rexrode, Kathryn; Jimenez-Conde, Jordi; Schmidt, Reinhold; Grewal, Raji P.; Sacco, Ralph; Ribases, Marta; Rundek, Tatjana; Rosand, Jonathan; Dichgans, Martin 
ORCID: https://orcid.org/0000-0002-0654-387X; Lee, Jin-Moo; Langefeld, Carl D.; Kittner, Steven J.; Markus, Hugh S.; Woo, Daniel und Malik, Rainer
(2019):
Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls.
In: Circulation-Genomic and Precision Medicine, Bd. 12, Nr. 7, e002338
[PDF, 502kB]
ORCID: https://orcid.org/0000-0002-0654-387X; Lee, Jin-Moo; Langefeld, Carl D.; Kittner, Steven J.; Markus, Hugh S.; Woo, Daniel und Malik, Rainer
(2019):
Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls.
In: Circulation-Genomic and Precision Medicine, Bd. 12, Nr. 7, e002338
[PDF, 502kB]
Rutten-Jacobs, Loes C. A.; Tozer, Daniel J.; Düring, Marco; Malik, Rainer; Dichgans, Martin; Markus, Hugh S. und Traylor, Matthew
(2018):
Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia.
In: Stroke, Bd. 49, Nr. 6: S. 1340-1347
[PDF, 1MB]
Rutten-Jacobs, Loes C. A.; Traylor, Matthew; Adib-Samii, Poneh; Thijs, Vincent; Sudlow, Cathie; Rothwell, Peter M.; Boncoraglio, Giorgio; Dichgans, Martin; Meschia, James; Maguire, Jane; Levi, Christopher; Rost, Natalia S.; Rosand, Jonathan; Hassan, Ahamad; Bevan, Steve und Markus, Hugh S.
(2016):
Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease Subtype.
In: Stroke, Bd. 47, Nr. 3: S. 646-651
Traylor, Matthew; Rutten-Jacobs, Loes C. A.; Thijs, Vincent; Holliday, Elizabeth G.; Levi, Chris; Bevan, Steve; Malik, Rainer; Boncoraglio, Giorgio; Sudlow, Cathie; Rothwell, Peter M.; Dichgans, Martin und Markus, Hugh S.
(2016):
Genetic Associations With White Matter Hyperintensities Confer Risk of Lacunar Stroke.
In: Stroke, Bd. 47, Nr. 5: S. 1174-1179