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robin lemmens
robin lemmens
UZ leuven, KU Leuven
Verified email at vib-kuleuven.be
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Cited by
Cited by
Year
MRI-guided thrombolysis for stroke with unknown time of onset
G Thomalla, CZ Simonsen, F Boutitie, G Andersen, Y Berthezene, ...
New England Journal of Medicine 379 (7), 611-622, 2018
12262018
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ...
Nature genetics 50 (4), 524-537, 2018
11962018
Dabigatran for prevention of stroke after embolic stroke of undetermined source
HC Diener, RL Sacco, JD Easton, CB Granger, RA Bernstein, S Uchiyama, ...
New England Journal of Medicine 380 (20), 1906-1917, 2019
6172019
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
M Traylor, M Farrall, EG Holliday, C Sudlow, JC Hopewell, YC Cheng, ...
The Lancet Neurology 11 (11), 951-962, 2012
5782012
EU-Wide Cross-Sectional Observational Study of Lipid-Modifying Therapy Use in Secondary and Primary Care: the DA VINCI study
KK Ray, B Molemans, WM Schoonen, P Giovas, S Bray, G Kiru, J Murphy, ...
European journal of preventive cardiology 28 (11), 1279-1289, 2021
5282021
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
MA Van Es, JH Veldink, CGJ Saris, HM Blauw, PWJ van Vught, A Birve, ...
Nature genetics 41 (10), 1083-1087, 2009
4342009
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
International Stroke Genetics Consortium (ISGC), ...
Nature genetics 44 (3), 328-333, 2012
4252012
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans
A Van Hoecke, L Schoonaert, R Lemmens, M Timmers, KA Staats, ...
Nature medicine 18 (9), 1418-1422, 2012
3442012
Variants of the elongator protein 3 ( ELP3 ) gene are associated with motor neuron degeneration
CL Simpson, R Lemmens, K Miskiewicz, WJ Broom, VK Hansen, ...
Human molecular genetics 18 (3), 472-481, 2009
3362009
A randomized trial of intravenous alteplase before endovascular treatment for stroke
NE LeCouffe, M Kappelhof, KM Treurniet, LA Rinkel, AE Bruggeman, ...
New England journal of medicine 385 (20), 1833-1844, 2021
2982021
Acute cerebrovascular disease in the young: the Stroke in Young Fabry Patients study
A Rolfs, F Fazekas, U Grittner, M Dichgans, P Martus, M Holzhausen, ...
Stroke 44 (2), 340-349, 2013
2882013
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study
MA Van Es, PW Van Vught, HM Blauw, L Franke, CG Saris, PM Andersen, ...
The Lancet Neurology 6 (10), 869-877, 2007
2792007
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis
MA Van Es, PWJ Van Vught, HM Blauw, L Franke, CGJ Saris, ...
Nature genetics 40 (1), 29-31, 2008
2732008
Lipoprotein (a) and stroke: a meta-analysis of observational studies
B Smolders, R Lemmens, V Thijs
Stroke 38 (6), 1959-1966, 2007
2552007
Etiology of first‐ever ischaemic stroke in European young adults: the 15 cities young stroke study
N Yesilot Barlas, J Putaala, U Waje‐Andreassen, S Vassilopoulou, ...
European journal of neurology 20 (11), 1431-1439, 2013
2392013
Demographic and geographic vascular risk factor differences in European young adults with ischemic stroke: the 15 cities young stroke study
J Putaala, N Yesilot, U Waje-Andreassen, J Pitkäniemi, S Vassilopoulou, ...
Stroke 43 (10), 2624-2630, 2012
2172012
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
MA Van Es, HJ Schelhaas, PWJ Van Vught, N Ticozzi, PM Andersen, ...
Annals of neurology 70 (6), 964-973, 2011
2112011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
MA Van Es, HJ Schelhaas, PWJ Van Vught, N Ticozzi, PM Andersen, ...
Annals of neurology 70 (6), 964-973, 2011
2112011
Review of perfusion imaging in acute ischemic stroke: from time to tissue
J Demeestere, A Wouters, S Christensen, R Lemmens, MG Lansberg
Stroke 51 (3), 1017-1024, 2020
1862020
Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish
R Lemmens, A Van Hoecke, N Hersmus, V Geelen, I D'Hollander, V Thijs, ...
Human molecular genetics 16 (19), 2359-2365, 2007
1792007
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