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1.
Bakker, M.K.* et al.: Genetic risk Score for intracranial aneurysms: Prediction of subarachnoid hemorrhage and role in clinical heterogeneity. Stroke 54, 810-818 (2023)
2.
Mai, H. et al.: Spatial proteomics analysis of soft and stiff regions in human acute arterial thrombus. Stroke 54, 1636-1644 (2023)
3.
Hämmerle, M.* et al.: A family and a genome-wide polygenic risk score are independentlyassociated with stroke in a population-based study. Stroke 53, 2331-2339 (2022)
4.
Camen, S.* et al.: Cardiac Troponin I and incident stroke in European cohorts: Insights from the BiomarCaRE project, Stroke 51, 2770-2777 (2020)
5.
Ebner, M.* et al.: Emergency coagulation assessment during treatment with direct oral anticoagulants: Limitations and solutions. Stroke 48, 2457-2463 (2017)
6.
Boeckh-Behrens, T.* et al.: Thrombus histology suggests cardioembolic cause in cryptogenic stroke. Stroke 47, 1864-1871 (2016)
7.
Cheng, Y.C.* et al.: Genome-wide association analysis of young onset stroke identifies a locus on chromosome 10q25 near HABP2. Stroke 47, 307-316 (2016)
8.
Dichgans, M.* et al.: Shared genetic susceptibility to ischemic stroke and coronary artery disease: A genome-wide analysis of common variants. Stroke 45, 24-36 (2014)
9.
Opherk, C.* et al.: Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL. Stroke 45, 968-972 (2014)
10.
Niv, F.* et al.: Aberrant neurogenesis after stroke: A retroviral cell labeling study. Stroke 43, 2468-2475 (2012)
11.
Kronenberg, G.* et al.: Modulation of fate determinants Olig2 and Pax6 in resident glia evokes spiking neuroblasts in a model of mild brain ischemia. Stroke 41, 2944-2999 (2010)
12.
Freilinger, T.* et al.: Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations. Stroke 40, 970-972 (2009)
13.
Bevan, S.* et al.: Genetic variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke - A replication study in two independent populations. Stroke 39, 1109-1114 (2008)
14.
Gschwendtner, A.* et al.: Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans. Stroke 39, 1593-1596 (2008)
15.
Löhmussaar, E.* et al.: ALOX5AP gene and the PDE4D gene in a central European population of stroke patients. Stroke 36, 731-736 (2005)
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