Ghent University Academic Bibliography

Your filters: cql: author="Rademakers, Rosa" or (type any "bookEditor issueEditor" and editor="Rademakers, Rosa")

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Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health

Jolien Perneel, Miranda Lastra Osua, Sara Alidadiani, Nele Peeters, Linus De Witte, Bavo Heeman, Simona Manzella, Riet De Rycke (UGent) , Mieu Brooks, Ralph B. Perkerson, et al.

(2025) MOLECULAR NEURODEGENERATION. 20(1).
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Local structural preferences in shaping tau amyloid polymorphism

Nikolaos Louros, Martin Wilkinson, Grigoria Tsaka, Meine Ramakers, Chiara Morelli, Teresa Garcia, Rodrigo Gallardo, Sam D'Haeyer (UGent) , Vera Goossens (UGent) , Dominique Audenaert (UGent) , et al.

(2024) NATURE COMMUNICATIONS. 15(1).
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Scywalker : scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing

Peter De Rijk, Tijs Watzeels, Fahri Küçükali, Jasper Van Dongen, Júlia Faura, Patrick Willems (UGent) , Lara De Deyn, Lena Duchateau, Carolin Seyfferth (UGent) , Thomas Eekhout (UGent) , et al.

(2024) BIOINFORMATICS. 40(9).
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Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family

Daniel Pirici, Rik Vandenberghe, Rosa Rademakers, Bart Dermaut (UGent) , Marc Cruts, Krist'l Vennekens, Ivy Cuijt, Ursula Lubke, Chantal Ceuterick, Jean-Jacques Martin, et al.

(2006) JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 65(3). p.289-301
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Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia

Sebastiaan Engelborghs, Bart Dermaut (UGent) , Peter Mariën, Anoek Symons, Ellen Vloeberghs, Karen Maertens, Nore Somers, Johan Goeman, Rosa Rademakers, Marleen Van den Broeck, et al.

(2006) NEUROBIOLOGY OF AGING. 27(2). p.285-292
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- Journal Article
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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Marc Cruts, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Hans Wils, Daniel Pirici, Rosa Rademakers, Rik Vandenberghe, Bart Dermaut (UGent) , Jean-Jacques Martin, et al.

(2006) NATURE. 442(7105). p.920-924
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Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum

Bart Dermaut (UGent) , Samir Kumar-Singh, Rosa Rademakers, Jessie Theuns, Marc Cruts and Christine Van Broeckhoven

(2005) TRENDS IN GENETICS. 21(12). p.664-672
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Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

Marc Cruts, Rosa Rademakers, Ilse Gijselinck, Julie van der Zee, Bart Dermaut (UGent) , Tim de Pooter, Peter de Rijk, Jurgen Del-Favero and Christine van Broeckhoven

(2005) HUMAN MOLECULAR GENETICS. 14(13). p.1753-1762
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Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample

Rosa Rademakers, Marc Cruts, Kristel Sleegers, Bart Dermaut (UGent) , Jessie Theuns, Yurii Aulchenko, Stefan Weckx, Tim De Pooter, Marleen Van den Broeck, Ellen Corsmit, et al.

(2005) AMERICAN JOURNAL OF HUMAN GENETICS. 77(4). p.643-652
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- Conference Paper
- C3
A novel presenilin 1 mutation (gly183val) is associated with Pick's disease in the absence of β-amyloid plaques

Bart Dermaut (UGent) , Samir Kumar-Singh, Sebastiaan Engelborghs, Jessie Theuns, Rosa Rademakers, Karin Peeters, Stephan Claes, Marc Cruts, Jean-Jacques Martin, Peter De Deyn, et al.

(2004) NEUROBIOLOGY OF AGING. 25(suppl. 2). p.S61-S61

Academic Bibliography

Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health

Local structural preferences in shaping tau amyloid polymorphism

Scywalker : scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing

Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family

Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample

A novel presenilin 1 mutation (gly183val) is associated with Pick's disease in the absence of β-amyloid plaques

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