Publications by authors named "Marc Cruts"

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Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.
Kohji Mori, Thomas Arzberger, Friedrich A Grässer, Ilse Gijselinck, Stephanie May, Marc Cruts

Acta Neuropathol· October 2024

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Data Mining: Applying the AD&FTD Mutation Database to Progranulin.
Marc Cruts, Christine Van Broeckhoven

Methods Mol Biol· March 2019

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NanoPack: visualizing and processing long-read sequencing data.
Wouter De Coster, Svenn D'Hert, Darrin T Schultz, Marc Cruts, Christine Van Broeckhoven

Bioinformatics· August 2018

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Clinical variability and onset age modifiers in an extended Belgian GRN founder family.
Eline Wauters, Sara Van Mossevelde, Kristel Sleegers, Julie van der Zee, Sebastiaan Engelborghs, Marc Cruts

Neurobiol Aging· July 2018

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Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.
Stéphanie Philtjens, Sara Van Mossevelde, Julie van der Zee, Eline Wauters, Lubina Dillen, Marc Cruts

Neurobiol Aging· June 2018

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The Genetics of Expansions.
Ilse Gijselinck, Marc Cruts, Christine Van Broeckhoven

Cold Spring Harb Perspect Med· April 2018

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Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort.
Jan Verheijen, Julie van der Zee, Ilse Gijselinck, Tobi Van den Bossche, Lubina Dillen, Marc Cruts

Neurobiol Aging· February 2018

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Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family.
Anne Sieben, Sara Van Mossevelde, Eline Wauters, Sebastiaan Engelborghs, Julie van der Zee, Marc Cruts

Alzheimers Res Ther· January 2018

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Familial primary lateral sclerosis or dementia associated with Arg573Gly mutation.
Estrella Gómez-Tortosa, Julie Van der Zee, María Ruggiero, Ilse Gijselinck, Jesús Esteban-Pérez, Marc Cruts

J Neurol Neurosurg Psychiatry· November 2017

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Modifiers of GRN-Associated Frontotemporal Lobar Degeneration.
Eline Wauters, Sara Van Mossevelde, Julie Van der Zee, Marc Cruts, Christine Van Broeckhoven

Trends Mol Med· October 2017

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Relationship between C9orf72 repeat size and clinical phenotype.
Sara Van Mossevelde, Julie van der Zee, Marc Cruts, Christine Van Broeckhoven

Curr Opin Genet Dev· June 2017

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Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Kristel Sleegers, Jan De Bleecker, Marc Cruts

JAMA Neurol· April 2017

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TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Marc Cruts

Hum Mutat· March 2017

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Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin.
Gernot Kleinberger, Anja Capell, Nathalie Brouwers, Katrin Fellerer, Kristel Sleegers, Marc Cruts

Neurobiol Aging· March 2016

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Clinical features of TBK1 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, Marc Cruts

Brain· February 2016

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Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD.
Steven Boeynaems, Elke Bogaert, Emiel Michiels, Ilse Gijselinck, Anne Sieben, Marc Cruts

Sci Rep· February 2016

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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, Stéphanie Philtjens, Marc Cruts

Neurology· December 2015

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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, Stéphanie Philtjens, Gernot Kleinberger, Sara Van Mossevelde, Julie van der Zee, Marc Cruts

Acta Neuropathol Commun· November 2015

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Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations.
Karolien Bettens, Steven Vermeulen, Caroline Van Cauwenberghe, Bavo Heeman, Bob Asselbergh, Marc Cruts

Mol Neurodegener· July 2015

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Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.
Jessie Theuns, Aline Verstraeten, Kristel Sleegers, Eline Wauters, Ilse Gijselinck, Marc Cruts

Neurology· November 2014

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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
Julie van der Zee, Tim Van Langenhove, Gabor G Kovacs, Lubina Dillen, William Deschamps, Marc Cruts

Acta Neuropathol· September 2014

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Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.
Shai Carmi, Ken Y Hui, Ethan Kochav, Xinmin Liu, James Xue, Marc Cruts

Nat Commun· September 2014

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Frontotemporal dementia and its subtypes: a genome-wide association study.
Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, Jonathan D Rohrer, Adaikalavan Ramasamy, Marc Cruts

Lancet Neurol· July 2014

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TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
Michael D Gallagher, Eunran Suh, Murray Grossman, Lauren Elman, Leo McCluskey, Marc Cruts

Acta Neuropathol· March 2014

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Promoter DNA methylation regulates progranulin expression and is altered in FTLD.
Julia Banzhaf-Strathmann, Rainer Claus, Oliver Mücke, Kristin Rentzsch, Julie van der Zee, Marc Cruts

Acta Neuropathol Commun· May 2013

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