Researcher
Lubina Dillen
- Keywords:Biology
- Disciplines:Animal biology, Bioinformatics and computational biology, Ecology, Evolutionary biology, General biology, Genetics, Microbiology, Molecular and cell biology, Plant biology, Systems biology, Other biological sciences, Other natural sciences
Affiliations
- Evolutionary ecology group (EVECO) (Research group)
Member
From1 Oct 2005 → 31 Mar 2010
Publications
11 - 20 of 28
- A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimers disease(2016)
Authors: 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.
Pages: 213 - 224 - Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD(2016)
Authors: Julie van der Zee, Peter Mariën, Roeland Crols, Sara Van Mossevelde, Lubina Dillen, Federica Perrone, Sebastiaan Engelborghs, Jo Verhoeven, Tine D'aes, Chantal De Groote, et al.
Pages: 1 - 8 - Rare variants in PLD3 do not affect risk for early-onset Alzheimer disease in a European consortium cohort(2015)
Authors: Rita Cacace, Tobi Van den Bossche, Sebastiaan Engelborghs, Nathalie Geerts, Annelies Laureys, Lubina Dillen, Caroline Graff, Hakan Thonberg, Huei-Hsin Chiang, Pau Pastor, et al.
Pages: 1226 - 1235 - Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia(2015)
Authors: Elise Cuyvers, Julie van der Zee, Karolien Bettens, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Caroline Robberecht, Lubina Dillen, Céline Merlin, Nathalie Geerts, Caroline Graff, et al.
- Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains(2015)
Authors: Jonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, Sara Van Mossevelde, Julie van der Zee, Rita Cacace, Sebastiaan Engelborghs, Anne Sieben, Julia Banzhaf-Strathmann, Lubina Dillen, et al.
- Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation(2014)
Authors: Marc Suárez-Calvet, Oriol Dols-Icardo, Albert Lladó, Julie van der Zee, Lubina Dillen, Christine Van Broeckhoven, et al.
Pages: 684 - 691 - Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration(2014)
Authors: Julie van der Zee, Tim Van Langenhove, Gabor G. Kovacs, Lubina Dillen, Sebastiaan Engelborghs, Anne Sieben, Katrien Smets, Céline Merlin, Annelies Laureys, Marleen Van den Broeck, et al.
Pages: 397 - 410 - Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation(2013)
Authors: Catarina Chester, Mamede de Carvalho, Gabriel Miltenberger, Sónia Pereira, Lubina Dillen, Julie van der Zee, Christine Van Broeckhoven, Alexandre de Mendonça
Pages: 70 - 72 - A Pan-European study of the **C9orf72** repeat associated with FTLD(2013)
Authors: Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Kristel Sleegers, Anne Sieben, Veerle Bäumer, et al.
Pages: 363 - 373 - Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients(2013)
Authors: Lubina Dillen, Tim Van Langenhove, Sebastiaan Engelborghs, Céline Merlin, Patrick Cras, Albena Jordanova, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, et al.
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