|
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Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease
52 auth.
J. Theuns,
Aline Verstraeten,
K. Sleegers,
Eline Wauters,
I. Gijselinck,
S. Smolders,
D. Crosiers,
E. Corsmit,
E. Elinck,
Manu Sharma,
R. Krüger,
S. Lesage,
Alexis Brice,
Sun Ju Chung,
Mi-Jung Kim,
...
Young Jin Kim,
Owen A. Ross,
Z. Wszolek,
E. Rogaeva,
Z. Xi,
Anthony E. Lang,
C. Klein,
A. Weissbach,
G. Mellick,
P. Silburn,
G. Hadjigeorgiou,
E. Dardiotis,
Nobutaka Hattori,
K. Ogaki,
E. Tan,
Yi Zhao,
J. Aasly,
E. M. Valente,
Simona Petrucci,
G. Annesi,
Aldo Quattrone,
C. Ferrarese,
L. Brighina,
Angela B Deutschländer,
A. Puschmann,
Christer Nilsson,
Gaëtan Garraux,
M. LeDoux,
R. Pfeiffer,
M. Boczarska-Jedynak,
G. Opala,
D. Maraganore,
S. Engelborghs,
P. D. de Deyn,
P. Cras,
M. Cruts,
C. van Broeckhoven
|
5 |
2014 |
5
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|
🐜
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Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson’s disease and increase susceptibility to dementia in a Flanders-Belgian cohort
10 auth.
D. Crosiers,
A. Verstraeten,
Eline Wauters,
S. Engelborghs,
K. Peeters,
Maria Mattheijssens,
...
P. Deyn,
J. Theuns,
C. Broeckhoven,
P. Cras
|
4 |
2016 |
4
🐜
|
|
🦁
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Modifiers of GRN-Associated Frontotemporal Lobar Degeneration.
Eline Wauters,
Sara Van Mossevelde,
J. van der Zee,
M. Cruts,
C. van Broeckhoven
|
4 |
2017 |
4
🦁
|
|
🐜
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Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
41 auth.
Stéphanie Philtjens,
S. V. Mossevelde,
J. Zee,
Eline Wauters,
L. Dillen,
M. Vandenbulcke,
R. Vandenberghe,
A. Ivanoiu,
A. Sieben,
Christiana Willems,
L. Benussi,
R. Ghidoni,
G. Binetti,
B. Borroni,
A. Padovani,
...
P. Pastor,
M. Diez-Fairen,
M. Aguilar,
A. Mendonça,
G. Miltenberger-Miltenyi,
I. Hernández,
M. Boada,
A. Ruiz,
B. Nacmias,
S. Sorbi,
M. R. Almeida,
I. Santana,
J. Clarimón,
A. Lleó,
G. Frisoni,
Raquel Sánchez-Valle,
A. Lladó,
E. Gómez-Tortosa,
E. Gelpí,
M. Broeck,
K. Peeters,
P. Cras,
P. Deyn,
S. Engelborghs,
M. Cruts,
C. Broeckhoven
|
4 |
2018 |
4
🐜
|
|
🐜
|
Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population
15 auth.
A. Verstraeten,
Eline Wauters,
D. Crosiers,
Bram Meeus,
E. Corsmit,
E. Elinck,
Maria Mattheijssens,
K. Peeters,
P. Cras,
B. Pickut,
...
R. Vandenberghe,
S. Engelborghs,
P. Deyn,
C. Broeckhoven,
J. Theuns
|
4 |
2012 |
4
🐜
|
|
🦁
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Clinical variability and onset age modifiers in an extended Belgian GRN founder family
33 auth.
Eline Wauters,
Sara Van Mossevelde,
K. Sleegers,
J. van der Zee,
S. Engelborghs,
A. Sieben,
R. Vandenberghe,
Stéphanie Philtjens,
M. Van den Broeck,
K. Peeters,
Ivy Cuijt,
Wouter De Coster,
Tim van Langenhove,
P. Santens,
A. Ivanoiu,
...
P. Cras,
J. D. De Bleecker,
J. Versijpt,
R. Crols,
N. de Klippel,
Jean-Jacques Martin,
P. D. de Deyn,
M. Cruts,
C. van Broeckhoven,
J. Goeman,
Dirk Nuytten,
M. Vandenbulcke,
A. Michotte,
E. Salmon,
O. Deryck,
B. Bergmans,
Christiana Willems,
Jean-Willem Delbeck
|
4 |
2018 |
4
🦁
|
|
🐬
|
Uncovering the impact of noncoding variants in neurodegenerative brain diseases.
Alexandros Frydas,
Eline Wauters,
J. van der Zee,
C. van Broeckhoven
|
4 |
2021 |
4
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|
