BetterScholar BetterScholar

J. Theuns

Human Mutation, JAMA Neurology, Brain : a journal of neurology, Lancet Neurology, Annals of Neurology, Trends in Genetics, Human Molecular Genetics, American Journal of Human Genetics Show more
11
Role
Title
Level Year L/R
🐬 Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update
Karen Nuytemans, J. Theuns, M. Cruts, C. van Broeckhoven 		9 2010
9
🐬
🐬 Locus-Specific Mutation Databases for Neurodegenerative Brain Diseases
M. Cruts, J. Theuns, C. van Broeckhoven 		8 2012
8
🐬
🐜 A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies.
58 auth. M. Nalls, R. Durán, G. Lopez, M. Kurzawa-Akanbi, I. McKeith, P. Chinnery, C. Morris, J. Theuns, D. Crosiers, P. Cras, S. Engelborghs, P. D. de Deyn, C. van Broeckhoven, D. Mann, J. Snowden, ... S. Pickering-Brown, Nicola A. Halliwell, Y. Davidson, L. Gibbons, Jenny Harris, U. Sheerin, J. Bras, J. Hardy, L. Clark, K. Marder, L. Honig, D. Berg, W. Maetzler, K. Brockmann, T. Gasser, F. Novellino, A. Quattrone, G. Annesi, E. V. De Marco, E. Rogaeva, M. Masellis, S. Black, J. Bilbao, T. Foroud, B. Ghetti, W. Nichols, N. Pankratz, G. Halliday, S. Lesage, S. Klebe, A. Durr, C. Duyckaerts, A. Brice, B. Giasson, J. Trojanowski, H. Hurtig, N. Tayebi, Claudia S Landazabal, M. A. Knight, Margaux F. Keller, A. Singleton, T. Wolfsberg, E. Sidransky 		8 2013
8
🐜
🐜 APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.
10 auth. K. Sleegers, N. Brouwers, I. Gijselinck, J. Theuns, D. Goossens, J. Wauters, ... J. Del-Favero, M. Cruts, C. V. van Duijn, C. van Broeckhoven 		8 2006
8
🐜
🐜 Mean age‐of‐onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
10 auth. S. Kumar-Singh, J. Theuns, Bianca Van Broeck, D. Pirici, K. Vennekens, E. Corsmit, ... M. Cruts, B. Dermaut, Rong Wang, C. van Broeckhoven 		8 2006
8
🐜
🐜 Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study
69 auth. O. Ross, A. Soto-Ortolaza, M. Heckman, J. Aasly, Nadine Abahuni, G. Annesi, Justin A. Bacon, S. Bardien, M. Bozi, A. Brice, L. Brighina, C. Broeckhoven, J. Carr, M. Chartier-Harlin, M. Chartier-Harlin, ... E. Dardiotis, E. Dardiotis, D. Dickson, N. Diehl, A. Elbaz, A. Elbaz, C. Ferrarese, A. Ferraris, B. Fiske, J. Gibson, Rachel Gibson, G. Hadjigeorgiou, G. Hadjigeorgiou, N. Hattori, J. Ioannidis, J. Ioannidis, B. Jasińska‐Myga, B. Jeon, Y. Kim, C. Klein, R. Krüger, Elli Kyratzi, S. Lesage, S. Lesage, S. Lesage, Chin-Hsien Lin, T. Lynch, D. Maraganore, G. Mellick, E. Mutez, E. Mutez, C. Nilsson, G. Opala, S. Park, A. Puschmann, A. Quattrone, M. Sharma, P. Silburn, Y. Sohn, L. Stefanis, V. Tadić, J. Theuns, H. Tomiyama, R. Uitti, E. Valente, S. Loo, D. Vassilatis, C. Vilariño-Güell, L. White, K. Wirdefeldt, Z. Wszolek, R. Wu, M. Farrer, M. Farrer 		8 2011
8
🐜
🐜 A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
62 auth. J. van der Zee, I. Gijselinck, L. Dillen, Tim van Langenhove, J. Theuns, S. Engelborghs, Stéphanie Philtjens, M. Vandenbulcke, K. Sleegers, A. Sieben, Veerle Bäumer, Githa Maes, E. Corsmit, B. Borroni, A. Padovani, ... S. Archetti, R. Perneczky, J. Diehl-Schmid, A. de Mendonça, G. Miltenberger-Miltenyi, S. Pereira, J. Pimentel, B. Nacmias, S. Bagnoli, S. Sorbi, C. Graff, H. Chiang, M. Westerlund, Raquel Sánchez-Valle, A. Lladó, E. Gelpí, I. Santana, M. R. Almeida, B. Santiago, G. Frisoni, O. Zanetti, C. Bonvicini, M. Synofzik, W. Maetzler, Jennifer Müller vom Hagen, L. Schöls, M. Heneka, F. Jessen, R. Matěj, E. Parobková, G. Kovacs, T. Ströbel, Stayko Sarafov, I. Tournev, A. Jordanova, A. Danek, T. Arzberger, G. Fabrizi, S. Testi, E. Salmon, P. Santens, Jean-Jacques Martin, P. Cras, R. Vandenberghe, P. D. de Deyn, M. Cruts, C. van Broeckhoven 		8 2012
8
🐜
🐜 A novel presenilin 1 mutation associated with Pick's disease but not β‐amyloid plaques
16 auth. B. Dermaut, S. Kumar-Singh, S. Engelborghs, J. Theuns, R. Rademakers, J. Saerens, B. Pickut, K. Peeters, M. Van den Broeck, K. Vennekens, ... S. Claes, M. Cruts, P. Cras, Jean-Jacques Martin, C. van Broeckhoven, P. D. de Deyn 		7 2004
7
🐜
🐬 Progress in unraveling the genetic etiology of Parkinson disease in a genomic era.
A. Verstraeten, J. Theuns, C. van Broeckhoven 		7 2015
7
🐬
🐜 Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3.
10 auth. M. Cruts, H. Backhovens, S. Y. Wang, G. Van Gassen, J. Theuns, C. de Jonghe, ... A. Wehnert, J. De Voecht, G. De Winter, P. Cras 		7 1995
7
🐜
🦁 Promoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease.
10 auth. J. Theuns, N. Brouwers, S. Engelborghs, K. Sleegers, Veerle Bogaerts, E. Corsmit, ... Tim De Pooter, C. V. van Duijn, P. D. de Deyn, C. van Broeckhoven 		7 2006
7
🦁