Onderzoeker
Lubina Dillen
- Trefwoorden:Biologie
- Disciplines:Dierkundige biologie, Bio-informatica en computationele biologie, Ecologie, Evolutiebiologie, Algemene biologie, Genetica, Microbiologie, Moleculaire en celbiologie, Plantenbiologie, Systeembiologie, Andere biologische wetenschappen, Andere natuurwetenschappen
Affiliaties
- Evolutionaire ecologie (EVECO) (Onderzoeksgroep)
Lid
Vanaf1 okt 2005 → 31 mrt 2010
Publicaties
1 - 10 van 28
- TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early-onset autosomal dominant dementia with amyloid load and parkinsonism(2023)
Auteurs: Estrella Gomez-Tortosa, Yalda Baradaran Heravi, Lubina Dillen, Nila Roy Choudhury, Pablo Aguero Rabes, Julian Perez-Perez, Cemile Kocoglu, M. Jose Sainz, Alicia Ruiz Gonzalez, Raquel Tellez, et al.
Pagina's: 2805 - 2815 - No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers(2021)
Auteurs: Cemile Kocoglu, Helena Gossye, Lubina Dillen, Sara Van Mossevelde, Jan L. De Bleecker, Rik Vandenberghe, Peter De Deyn, Kristel Sleegers, Patrick Cras, Sebastiaan Engelborghs, et al.
Pagina's: 145.e1 - 145.e4 - Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis(2021)
Auteurs: Julie van der Zee, Lubina Dillen, Yalda Baradaran Heravi, Helena Gossye, Cemile Kocoglu, Ivy Cuijt, Bart Dermaut, Anne Sieben, Jonathan Baets, Peter De Jonghe, et al.
- Sporadic Creutzfeldt-Jakob disease and other proteinopathies in comorbidity(2020)
Auteurs: Eva Parobkova, Julie van der Zee, Lubina Dillen, Christine Van Broeckhoven, Robert Rusina, Radoslav Matej
- Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia(2018)
Auteurs: Stéphanie Philtjens, Sara Van Mossevelde, Julie van der Zee, Eline Wauters, Lubina Dillen, Mathieu Vandenbulcke, Rik Vandenberghe, Adrian Ivanoiu, Anne Sieben, Christiana Willems, et al.
- Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort(2018)
Auteurs: Jan Verheijen, Julie van der Zee, Ilse Gijselinck, Tobi Van den Bossche, Lubina Dillen, Bavo Heeman, Estrella Gomez-Tortosa, Albert Llado, Raquel Sanchez-Valle, Caroline Graff, et al.
- No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients(2018)
Auteurs: Lubina Dillen, Hung Nguyen Phuoc, Sara Van Mossevelde, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Rik Vandenberghe, Philip Van Damme, Patrick Cras, Eric Salmon, Matthis Synofzik, et al.
- NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients(2018)
Auteurs: Hung Nguyen Phuoc, Sara Van Mossevelde, Lubina Dillen, Jan L. De Bleecker, Matthieu Moisse, Philip Van Damme, Christine Van Broeckhoven, Julie van der Zee, Sebastiaan Engelborghs, Roeland Crois, et al.
- Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease(2017)
Auteurs: Arne De Roeck, Tobi Van den Bossche, Julie van der Zee, Jan Verheijen, Wouter De Coster, Jasper Van Dongen, Lubina Dillen, Yalda Baradaran Heravi, Bavo Heeman, Raquel Sanchez-Valle, et al.
Pagina's: 475 - 487 - TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis(2017)
Auteurs: Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker, Ellen Gelpi, et al.
Pagina's: 297 - 309