Christine Van Broeckhoven

发表

SSHSuite: an integrated software package for analysis of large-scale suppression subtractive hybridization data.

Jurgen Del-Favero, Stefan Weckx, Peter De Rijk, 2004, BioTechniques.

NanoPack: visualizing and processing long read sequencing data

Wouter De Coster, Darrin T. Schultz, Marc Cruts, 2018 .

SNPbox: web-based high-throughput primer design with an eye for repetitive sequences.

Jurgen Del-Favero, Stefan Weckx, Peter De Rijk, 2007, Methods in molecular biology.

Common variation in GRB‐associated Binding Protein 2 (GAB2) and increased risk for Alzheimer dementia

Sebastiaan Engelborghs, Christine Van Broeckhoven, Kristel Sleegers, 2009, Human mutation.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Eden R Martin, Seth Love, Brian Lawlor, 2019, Nature Genetics.

Dense-core plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls.

John Hardy, Samir Kumar-Singh, Christine Van Broeckhoven, 2005, The American journal of pathology.

Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

Kenneth Offit, Diether Lambrechts, Gil Atzmon, 2014, Nature Communications.

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.

Patrick Santens, Karin Peeters, Rik Vandenberghe, 2008, Human molecular genetics.

Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects

Lars-Göran Nilsson, Thomas Karlsson, Lars Nyberg, 2012, PloS one.

Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update

Marc Cruts, Karen Nuytemans, Christine Van Broeckhoven, 2010, Human mutation.

Loss of progranulin function in frontotemporal lobar degeneration.

Marc Cruts, Christine Van Broeckhoven, C. van Broeckhoven, 2008, Trends in genetics : TIG.

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.

Eric Guedj, Valérie Hahn-Barma, Marie-Odile Habert, 2008, Brain : a journal of neurology.

Intraneuronal amyloid beta and reduced brain volume in a novel APP T714I mouse model for Alzheimer's disease.

Samir Kumar-Singh, Christine Van Broeckhoven, Annemie Van der Linden, 2008, Neurobiology of aging.

The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects.

Philippe Amouyel, Jean-Charles Lambert, Lars Bertram, 2010, Trends in genetics : TIG.

Molecular genetics of Alzheimer's disease: An update

Christine Van Broeckhoven, Kristel Sleegers, K. Sleegers, 2008, Annals of medicine.

Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome.

Wouter De Coster, Mojca Strazisar, Svenn D'Hert, 2019, Genome research.

TDP-43 loss-of-function causes neuronal loss due to defective steroid receptor-mediated gene program switching in Drosophila.

Stein Aerts, Jean-Charles Lambert, Julien Chapuis, 2013, Cell reports.

Locus-Specific Mutation Databases for Neurodegenerative Brain Diseases

Marc Cruts, Christine Van Broeckhoven, C. van Broeckhoven, 2012, Human mutation.

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease

Giuliano Binetti, Alberto Lleó, Juan Fortea, 2016, Acta Neuropathologica.

Reduced functional brain activity response in cognitively intact apolipoprotein E epsilon4 carriers.

Jonas Persson, Lars-Göran Nilsson, Lars Nyberg, 2006, Brain : a journal of neurology.

The role of ABCA7 in Alzheimer’s disease: evidence from genomics, transcriptomics and methylomics

Christine Van Broeckhoven, Kristel Sleegers, K. Sleegers, 2019, Acta Neuropathologica.

Pathogenesis of polyglutamine disorders: aggregation revisited.

Christine Van Broeckhoven, C. van Broeckhoven, A. Michalik, 2003, Human molecular genetics.

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Patrick Santens, Mathieu Vandenbulcke, Adrian Ivanoiu, 2015, Acta neuropathologica communications.

Parietal cortex activation predicts memory decline in apolipoprotein E-ϵϵ4 carriers

Jonas Persson, Lars-Göran Nilsson, Lars Nyberg, 2006, Neuroreport.

The genetic landscape of Alzheimer disease: clinical implications and perspectives

Christine Van Broeckhoven, Kristel Sleegers, K. Sleegers, 2015, Genetics in Medicine.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease.

Sebastiaan Engelborghs, Christine Van Broeckhoven, Eugeen Vanmechelen, 2007, Brain : a journal of neurology.

Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric.

Cornelia M van Duijn, Jean-Pierre Timmermans, Rong Wang, 2002, The American journal of pathology.

De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

Berten Ceulemans, Salmo Raskin, Jurgen Del-Favero, 2003, Human mutation.

Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

Aldo Quattrone, Nobutaka Hattori, Mariza de Andrade, 2006, JAMA.