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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study OA Ross, AI Soto-Ortolaza, MG Heckman, JO Aasly, N Abahuni, G Annesi, ... The Lancet Neurology 10 (10), 898-908, 2011 | 345 | 2011 |
Large-scale replication and heterogeneity in Parkinson disease genetic loci M Sharma, JPA Ioannidis, JO Aasly, G Annesi, A Brice, ... Neurology 79 (7), 659-667, 2012 | 157 | 2012 |
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DLB and PDD: a role for mutations in dementia and Parkinson disease genes? B Meeus, A Verstraeten, D Crosiers, S Engelborghs, M Van den Broeck, ... Neurobiology of aging 33 (3), 629. e5-629. e18, 2012 | 101 | 2012 |
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Mindfulness training among individuals with Parkinson’s disease: neurobehavioral effects B Pickut, S Vanneste, MA Hirsch, W Van Hecke, E Kerckhofs, P Mariën, ... Parkinson’s disease 2015 (1), 816404, 2015 | 75 | 2015 |
Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation D Crosiers, B Ceulemans, B Meeus, K Nuytemans, P Pals, ... Parkinsonism & related disorders 17 (2), 135-138, 2011 | 73 | 2011 |
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease J Theuns, A Verstraeten, K Sleegers, E Wauters, I Gijselinck, S Smolders, ... Neurology 83 (21), 1906-1913, 2014 | 67 | 2014 |
Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export S Martin, S Smolders, C Van den Haute, B Heeman, S van Veen, ... Acta Neuropathologica 139, 1001-1024, 2020 | 55 | 2020 |
Myoclonus and cerebellar ataxia following COVID‐19 F Dijkstra, T Van den Bossche, B Willekens, P Cras, D Crosiers Movement disorders clinical practice 7 (8), 974, 2020 | 50 | 2020 |
Non-motor symptoms in a Flanders-Belgian population of 215 Parkinson’s disease patients as assessed by the Non-Motor Symptoms Questionnaire D Crosiers, B Pickut, J Theuns, PP De Deyn, C Van Broeckhoven, ... American Journal of Neurodegenerative Disease 1 (2), 160, 2012 | 45 | 2012 |
Impulse control disorders in Parkinson’s disease: an overview from neurobiology to treatment E Maréchal, B Denoiseux, E Thys, D Crosiers, B Pickut, P Cras Journal of Neurology 262, 7-20, 2015 | 39 | 2015 |
Using global team science to identify genetic Parkinson’s disease worldwide EJ Vollstedt, M Kasten, C Klein Annals of neurology 86 (2), 153, 2019 | 33 | 2019 |
Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson’s disease and increase susceptibility to dementia in a Flanders-Belgian cohort D Crosiers, A Verstraeten, E Wauters, S Engelborghs, K Peeters, ... Neuroscience letters 629, 160-164, 2016 | 31 | 2016 |
GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population B Meeus, K Nuytemans, D Crosiers, S Engelborghs, P Pals, B Pickut, ... Neurobiology of aging 32 (2), 308-312, 2011 | 31 | 2011 |
Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population A Verstraeten, E Wauters, D Crosiers, B Meeus, E Corsmit, E Elinck, ... Neurobiology of aging 33 (8), 1844. e11-1844. e13, 2012 | 30 | 2012 |
Natural history study of STXBP1-developmental and epileptic encephalopathy into adulthood H Stamberger, D Crosiers, G Balagura, CM Bonardi, A Basu, G Cantalupo, ... Neurology 99 (3), e221-e233, 2022 | 28 | 2022 |
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease L Wang, JO Aasly, G Annesi, S Bardien, M Bozi, A Brice, J Carr, SJ Chung, ... Neurology 85 (15), 1283-1292, 2015 | 27 | 2015 |