| 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 | 1710 | 2006 |
| Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ... Acta neuropathologica 119, 1-4, 2010 | 1166 | 2010 |
| Identification of a novel plasmid-mediated colistin-resistance gene, mcr-2, in Escherichia coli, Belgium, June 2016 BB Xavier, C Lammens, R Ruhal, S Kumar-Singh, P Butaye, H Goossens, ... Eurosurveillance 21 (27), 30280, 2016 | 926 | 2016 |
| TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration H Wils, G Kleinberger, J Janssens, S Pereson, G Joris, I Cuijt, V Smits, ... Proceedings of the National Academy of Sciences 107 (8), 3858-3863, 2010 | 682 | 2010 |
| Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions VM Van Deerlin, PMA Sleiman, M Martinez-Lage, A Chen-Plotkin, ... Nature genetics 42 (3), 234-239, 2010 | 612 | 2010 |
| Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ... Acta neuropathologica 117, 15-18, 2009 | 488 | 2009 |
| Mean age‐of‐onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40 S Kumar‐Singh, J Theuns, B Van Broeck, D Pirici, K Vennekens, ... Human mutation 27 (7), 686-695, 2006 | 468 | 2006 |
| FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration H Urwin, KA Josephs, JD Rohrer, IR Mackenzie, M Neumann, A Authier, ... Acta neuropathologica 120, 33-41, 2010 | 309 | 2010 |
| Pathogenic APP mutations near the γ-secretase cleavage site differentially affect Aβ secretion and APP C-terminal fragment stability C De Jonghe, C Esselens, S Kumar-Singh, K Craessaerts, S Serneels, ... Human molecular genetics 10 (16), 1665-1671, 2001 | 305 | 2001 |
| A novel presenilin 1 mutation associated with Pick's disease but not β‐amyloid plaques B Dermaut, S Kumar‐Singh, S Engelborghs, J Theuns, R Rademakers, ... Annals of Neurology: Official Journal of the American Neurological …, 2004 | 264 | 2004 |
| In vivo and In vitro Interactions between Pseudomonas aeruginosa and Staphylococcus spp. A Hotterbeekx, S Kumar-Singh, H Goossens, S Malhotra-Kumar Frontiers in cellular and infection microbiology 7, 106, 2017 | 255 | 2017 |
| Angiogenic cytokines in mesothelioma: a study of VEGF, FGF‐1 and‐2, and TGF β expression S Kumar‐Singh, J Weyler, MJH Martin, PB Vermeulen, E Van Marck The Journal of pathology 189 (1), 72-78, 1999 | 232 | 1999 |
| Dense-core plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls S Kumar-Singh, D Pirici, E McGowan, S Serneels, C Ceuterick, J Hardy, ... The American journal of pathology 167 (2), 527-543, 2005 | 213 | 2005 |
| Nonfibrillar diffuse amyloid deposition due to a γ 42‐secretase site mutation points to an essential role for N‐truncated A β 42 in Alzheimer’s disease S Kumar-Singh, C De Jonghe, M Cruts, R Kleinert, R Wang, M Mercken, ... Human molecular genetics 9 (18), 2589-2598, 2000 | 213 | 2000 |
| Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS‐1 mutations that lead to exceptionally high amyloid‐β concentrations H Houlden, M Baker, E McGowan, P Lewis, M Hutton, R Crook, NW Wood, ... Annals of neurology 48 (5), 806-808, 2000 | 176 | 2000 |
| Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric S Kumar-Singh, P Cras, R Wang, JM Kros, J van Swieten, U Lübke, ... The American journal of pathology 161 (2), 507-520, 2002 | 160 | 2002 |
| 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 | 155 | 2007 |
| Antibody elution method for multiple immunohistochemistry on primary antibodies raised in the same species and of the same subtype D Pirici, L Mogoanta, S Kumar-Singh, I Pirici, C Margaritescu, ... Journal of Histochemistry & Cytochemistry 57 (6), 567-575, 2009 | 154 | 2009 |
| The risk for behavioural deficits is determined by the maternal immune response to prenatal immune challenge in a neurodevelopmental model S Missault, K Van den Eynde, WV Berghe, E Fransen, A Weeren, ... Brain, behavior, and immunity 42, 138-146, 2014 | 145 | 2014 |
| WT1 MUTATION IN MALIGNANT MESOTHELIOMA AND WT1 IMMUNOREACTIVITY IN RELATION TO p53 AND GROWTH FACTOR RECEPTOR EXPRESSION … S KUMAR‐SINGH, K SEGERS, U RODECK, H BACKHOVENS, ... The Journal of Pathology: A Journal of the Pathological Society of Great …, 1997 | 144 | 1997 |
Marc CrutsProfessor of Molecular Genomics在 molgen.vib-ua.be 的电子邮件经过验证
