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Anzahl der Publikationen: 4
Zeitschriftenartikel
Egle, Marco; Hilal, Saima; Tuladhar, Anil M.; Pirpamer, Lukas; Bell, Steven; Hofer, Edith; Duering, Marco; Wason, James; Morris, Robin G.; Dichgans, Martin 
ORCID: https://orcid.org/0000-0002-0654-387X; Schmidt, Reinhold; Tozer, Daniel J.; Barrick, Thomas R.; Chen, Christopher; Leeuw, Frank-Erik de und Markus, Hugh S.
(2022):
Determining the OPTIMAL DTI analysis method for application in cerebral small vessel disease.
In: Neuroimage: Clinical, Bd. 35, 103114
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-0654-387X; Schmidt, Reinhold; Tozer, Daniel J.; Barrick, Thomas R.; Chen, Christopher; Leeuw, Frank-Erik de und Markus, Hugh S.
(2022):
Determining the OPTIMAL DTI analysis method for application in cerebral small vessel disease.
In: Neuroimage: Clinical, Bd. 35, 103114
[PDF, 1MB]
Traylor, Matthew; Persyn, Elodie; Tomppo, Liisa; Klasson, Sofia; Abedi, Vida; Bakker, Mark K.; Torres, Nuria; Li, Linxin; Bell, Steven; Rutten-Jacobs, Loes; Tozer, Daniel J.; Griessenauer, Christoph J.; Zhang, Yanfei; Pedersen, Annie; Sharma, Pankaj; Jimenez-Conde, Jordi; Rundek, Tatjana; Grewal, Raji P.; Lindgren, Arne; Meschia, James F.; Salomaa, Veikko; Havulinna, Aki; Kourkoulis, Christina; Crawford, Katherine; Marini, Sandro; Mitchell, Braxton D.; Kittner, Steven J.; Rosand, Jonathan; Dichgans, Martin ORCID: https://orcid.org/0000-0002-0654-387X; Jern, Christina; Strbian, Daniel; Fernandez-Cadenas, Israel; Zand, Ramin; Ruigrok, Ynte; Rost, Natalia; Lemmens, Robin; Rothwell, Peter M.; Anderson, Christopher D.; Wardlaw, Joanna; Lewis, Cathryn M. und Markus, Hugh S.
(2021):
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
In: Lancet Neurology, Bd. 20, Nr. 5: S. 351-361
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-0654-387X; Jern, Christina; Strbian, Daniel; Fernandez-Cadenas, Israel; Zand, Ramin; Ruigrok, Ynte; Rost, Natalia; Lemmens, Robin; Rothwell, Peter M.; Anderson, Christopher D.; Wardlaw, Joanna; Lewis, Cathryn M. und Markus, Hugh S.
(2021):
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
In: Lancet Neurology, Bd. 20, Nr. 5: S. 351-361
[PDF, 1MB]
Traylor, Matthew; Tozer, Daniel J.; Croall, Iain D.; Ford, Danuta M. Lisiecka; Olorunda, Abiodun Olubunmi; Boncoraglio, Giorgio; Dichgans, Martin ORCID: https://orcid.org/0000-0002-0654-387X; Lemmens, Robin; Rosand, Jonathan; Rost, Natalia S.; Rothwell, Peter M.; Sudlow, Cathie L. M.; Thijs, Vincent; Rutten-Jacobs, Loes und Markus, Hugh S.
(2019):
Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n=11,226).
In: Neurology, Bd. 92, Nr. 8, E749-E757
[PDF, 399kB]
ORCID: https://orcid.org/0000-0002-0654-387X; Lemmens, Robin; Rosand, Jonathan; Rost, Natalia S.; Rothwell, Peter M.; Sudlow, Cathie L. M.; Thijs, Vincent; Rutten-Jacobs, Loes und Markus, Hugh S.
(2019):
Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n=11,226).
In: Neurology, Bd. 92, Nr. 8, E749-E757
[PDF, 399kB]
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]