Publications by authors named "Ellen Corsmit"

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Pilot Testing of the "Turbidimeter", a Simple, Universal Reader Intended to Complement and Enhance Bacterial Growth Detection in Manual Blood Culture Systems in Low-Resource Settings.
Barbara Barbé, Ellen Corsmit, Jasper Jans, Kamalpreet Kaur, Roel Baets

Diagnostics (Basel)· March 2022

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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, Ellen Corsmit

Neurology· November 2014

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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, Jessie Theuns, Ellen Corsmit, Ellen Corsmit

Hum Mutat· February 2013

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Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.
Jessie Theuns, David Crosiers, Luc Debaene, Karen Nuytemans, Bram Meeus, Ellen Corsmit

Mov Disord· September 2012

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Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population.
Aline Verstraeten, Eline Wauters, David Crosiers, Bram Meeus, Ellen Corsmit

Neurobiol Aging· August 2012

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DLB and PDD: a role for mutations in dementia and Parkinson disease genes?
Bram Meeus, Aline Verstraeten, David Crosiers, Sebastiaan Engelborghs, Marleen Van den Broeck, Ellen Corsmit

Neurobiol Aging· March 2012

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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.
Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee, Kristel Sleegers, Stéphanie Philtjens, Ellen Corsmit

Lancet Neurol· January 2012

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GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population.
Bram Meeus, Karen Nuytemans, David Crosiers, Sebastiaan Engelborghs, Philippe Pals, Ellen Corsmit

Neurobiol Aging· February 2011

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Comprehensive genetic and mutation analysis of familial dementia with Lewy bodies linked to 2q35-q36.
Bram Meeus, Karen Nuytemans, David Crosiers, Sebastiaan Engelborghs, Karin Peeters, Ellen Corsmit

J Alzheimers Dis· July 2010

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Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
Karen Nuytemans, Bram Meeus, David Crosiers, Nathalie Brouwers, Dirk Goossens, Ellen Corsmit

Hum Mutat· July 2009

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Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.
Veerle Bogaerts, Karen Nuytemans, Joke Reumers, Philippe Pals, Sebastiaan Engelborghs, Ellen Corsmit

Hum Mutat· June 2008

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Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response.
Ines Dierick, Joy Irobi, Sophie Janssens, Jessie Theuns, Robin Lemmens, Ellen Corsmit

Hum Mutat· August 2007

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Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease.
Nathalie Brouwers, Kristel Sleegers, Sebastiaan Engelborghs, Veerle Bogaerts, Sally Serneels, Ellen Corsmit

Brain· November 2006

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Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40.
Samir Kumar-Singh, Jessie Theuns, Bianca Van Broeck, Daniel Pirici, Krist'l Vennekens, Ellen Corsmit

Hum Mutat· July 2006

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Promoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease.
Jessie Theuns, Nathalie Brouwers, Sebastiaan Engelborghs, Kristel Sleegers, Veerle Bogaerts, Ellen Corsmit

Am J Hum Genet· June 2006

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High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
Rosa Rademakers, Stacey Melquist, Marc Cruts, Jessie Theuns, Jurgen Del-Favero, Ellen Corsmit

Hum Mol Genet· November 2005

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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, Jessie Theuns, Ellen Corsmit

Am J Hum Genet· October 2005

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Alzheimer-associated C allele of the promoter polymorphism -22C>T causes a critical neuron-specific decrease of presenilin 1 expression.
Jessie Theuns, Jacques Remacle, Richard Killick, Ellen Corsmit, Krist'l Vennekens

Hum Mol Genet· April 2003

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The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample.
Bart Dermaut, Jessie Theuns, Kristel Sleegers, Hiroshi Hasegawa, Marleen Van den Broeck, Ellen Corsmit

Am J Hum Genet· June 2002

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