| Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 M Cruts, I Gijselinck, J Van Der Zee, S Engelborghs, H Wils, D Pirici, ... Nature 442 (7105), 920-924, 2006 | 1679 | 2006 |
| A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene … I Gijselinck, T Van Langenhove, J van der Zee, K Sleegers, S Philtjens, ... The Lancet Neurology 11 (1), 54-65, 2012 | 769 | 2012 |
| Treatment of Parkinson's disease with pergolide and relation to restrictive valvular heart disease G Van Camp, A Flamez, B Cosyns, C Weytjens, L Muyldermans, ... The Lancet 363 (9416), 1179-1183, 2004 | 409 | 2004 |
| The genetics and neuropathology of frontotemporal lobar degeneration A Sieben, T Van Langenhove, S Engelborghs, JJ Martin, P Boon, P Cras, ... Acta neuropathologica 124, 353-372, 2012 | 354 | 2012 |
| A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats J van der Zee, I Gijselinck, L Dillen, T Van Langenhove, J Theuns, ... Human mutation 34 (2), 363-373, 2013 | 316 | 2013 |
| Bilingualism delays clinical manifestation of Alzheimer's disease EVY Woumans, P Santens, A Sieben, JAN Versijpt, M Stevens, W Duyck Bilingualism: Language and Cognition 18 (3), 568-574, 2015 | 217 | 2015 |
| Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation L Timmermann, KAM Pauls, K Wieland, R Jech, G Kurlemann, N Sharma, ... Brain 133 (3), 701-712, 2010 | 212 | 2010 |
| Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort I Gijselinck, S Van Mossevelde, J Van Der Zee, A Sieben, S Philtjens, ... Neurology 85 (24), 2116-2125, 2015 | 191 | 2015 |
| Characterization and functional studies of lipoproteins, lipid transfer proteins, and lecithin: cholesterol acyltransferase in CSF of normal individuals and patients with … N Demeester, G Castro, C Desrumaux, C De Geitere, JC Fruchart, ... Journal of lipid research 41 (6), 963-974, 2000 | 189 | 2000 |
| CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro J van der Zee, H Urwin, S Engelborghs, M Bruyland, R Vandenberghe, ... Human molecular genetics 17 (2), 313-322, 2008 | 183 | 2008 |
| Assessment of Neuroinflammation and Microglial Activation in Alzheimer’s Disease with Radiolabelled PK11195 and Single Photon Emission Computed TomographyA Pilot Study JJ Versijpt, F Dumont, KJ Van Laere, D Decoo, P Santens, K Audenaert, ... European neurology 50 (1), 39-47, 2003 | 179 | 2003 |
| Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family N Brouwers, K Nuytemans, J van der Zee, I Gijselinck, S Engelborghs, ... Archives of neurology 64 (10), 1436-1446, 2007 | 153 | 2007 |
| Mutations in SACS cause atypical and late-onset forms of ARSACS J Baets, T Deconinck, K Smets, D Goossens, P Van den Bergh, K Dahan, ... Neurology 75 (13), 1181-1188, 2010 | 148 | 2010 |
| Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia J van der Zee, I Le Ber, S Maurer‐Stroh, S Engelborghs, I Gijselinck, ... Human mutation 28 (4), 416-416, 2007 | 133 | 2007 |
| TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort J van der Zee, T Van Langenhove, G Kleinberger, K Sleegers, ... Brain 134 (3), 808-815, 2011 | 132 | 2011 |
| Task preparation processes related to reward prediction precede those related to task-difficulty expectation H Schevernels, RM Krebs, P Santens, MG Woldorff, CN Boehler NeuroImage 84, 639-647, 2014 | 125 | 2014 |
| Multisubject learning for common spatial patterns in motor-imagery BCI D Devlaminck, B Wyns, M Grosse-Wentrup, G Otte, P Santens Computational intelligence and neuroscience 2011, 8-8, 2011 | 124 | 2011 |
| Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort T Van Langenhove, J Van Der Zee, I Gijselinck, S Engelborghs, ... JAMA neurology 70 (3), 365-373, 2013 | 119 | 2013 |
| Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration J Van Der Zee, T Van Langenhove, GG Kovacs, L Dillen, W Deschamps, ... Acta neuropathologica 128, 397-410, 2014 | 118 | 2014 |
| Lateralized effects of subthalamic nucleus stimulation on different aspects of speech in Parkinson’s disease P Santens, M De Letter, J Van Borsel, J De Reuck, J Caemaert Brain and language 87 (2), 253-258, 2003 | 114 | 2003 |
