Ghent University Academic Bibliography

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Your filters: cql: author="van der Zee, Julie*" or (type exact bookEditor and editor="van der Zee, Julie*")

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Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD

Julie van der Zee, Peter Marien, Roeland Crols, Sara Van Mossevelde, Lubina Dillen, Federica Perrone, Sebastiaan Engelborghs, Jo Verhoeven, Tine D'aes, Chantal Ceuterick-De Groote, et al.

(2016) NEUROLOGY-GENETICS. 2(5).
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A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

Jan Verheijen, Tobi Van den Bossche, Julie van der Zee, Sebastiaan Engelborghs, Raquel Sanchez-Valle, Albert Llado, Caroline Graff, Hakan Thonberg, Pau Pastor, Sara Ortega-Cubero, et al.

(2016) ACTA NEUROPATHOLOGICA. 132(2). p.213-224
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Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Anne Sieben (UGent) , Tim Van Langenhove (UGent) , Jan De Bleecker (UGent) , Jonathan Baets, Mathieu Vandenbulcke, Koen Van Laere, et al.

(2016) BRAIN. 139. p.452-467
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Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Jonathan Janssens, Stephanie Philtjens, Gernot Kleinberger, Sara Van Mossevelde, Julie van der Zee, Rita Cacace, Sebastiaan Engelborghs, Anne Sieben (UGent) , Julia Banzhaf-Strathmann, Lubina Dillen, et al.

(2015) ACTA NEUROPATHOLOGICA COMMUNICATIONS. 3.
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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, Anne Sieben (UGent) , Stephanie Philtjens, Bavo Heeman, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Greet De Baets, Veerle Baumer, et al.

(2015) NEUROLOGY. 85(24). p.2116-2125
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Julie van der Zee, Tim Van Langenhove (UGent) , Gabor G Kovacs, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben (UGent) , Bart Dermaut (UGent) , et al.

(2014) ACTA NEUROPATHOLOGICA. 128(3). p.397-410
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

Elise Cuyvers, Karolien Bettens, Stéphanie Philtjens, Tim Van Langenhove (UGent) , Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, Nathalie Geerts, et al.

(2014) NEUROBIOLOGY OF AGING. 35(3). p.726.e11-726.e19
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A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats

Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove (UGent) , Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben (UGent) , et al.

(2013) HUMAN MUTATION. 34(2). p.363-373
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Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

Tim Van Langenhove (UGent) , Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Rik Vandenberghe, Mathieu Vandenbulcke, Jan De Bleecker (UGent) , Anne Sieben (UGent) , Jan Versijpt, Adrian Ivanoiu, et al.

(2013) JAMA NEUROLOGY. 70(3). p.365-373
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Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

Lubina Dillen, Tim Van Langenhove (UGent) , Sebastiaan Engelborghs, Mathieu Vandenbulcke, Stayko Sarafov, Ivailo Tournev, Celine Merlin, Patrick Cras, Rik Vandenberghe, Peter P De Deyn, et al.

(2013) NEUROBIOLOGY OF AGING. 34(6).

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Academic Bibliography

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

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