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Christine Van Broeckhoven biologiste belge ISNI Wikidata

Van Broeckhoven, C. (Christine), 1953- National Library of the Netherlands

VIAF ID: 288501792 (Personal)

Permalink: http://viaf.org/viaf/288501792

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Title Sources
Brein en branie National Library of the Netherlands
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis Wikidata
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder Wikidata
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Wikidata
Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population. Wikidata
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease Wikidata
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy Wikidata
Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene. Wikidata
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains. Wikidata
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21 Wikidata
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease Wikidata
Large-scale replication and heterogeneity in Parkinson disease genetic loci. Wikidata
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample Wikidata
Locus-specific mutation databases for neurodegenerative brain diseases Wikidata
Longer leukocyte telomere length is associated with smaller hippocampal volume among non-demented APOE ε3/ε3 subjects Wikidata
Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth. Wikidata
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort. Wikidata
Lymphoblast-derived integration-free iPSC lines from a female and male Alzheimer's disease patient expressing different copy numbers of a coding CNV in the Alzheimer risk gene CR1. Wikidata
Major affective disorders and schizophrenia: a common molecular signature? Wikidata
Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40. Wikidata
Mechanisms of granulin deficiency: lessons from cellular and animal models Wikidata
Messenger RNA electroporation of human monocytes, followed by rapid in vitro differentiation, leads to highly stimulatory antigen-loaded mature dendritic cells. Wikidata
Mijn hersenen dat ben ik! National Library of the Netherlands
Molecular genetics of early-onset Alzheimer's disease revisited Wikidata
Molecular pathogenesis of frontotemporal lobar degeneration: basic science seminar in neurology. Wikidata
Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3 Wikidata
Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis Wikidata
Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort. Wikidata
Mutations in SEPT9 cause hereditary neuralgic amyotrophy Wikidata
No added diagnostic value of non-phosphorylated tau fraction (p-taurel) in CSF as a biomarker for differential dementia diagnosis. Wikidata
No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease. Wikidata
Non-motor symptoms in a Flanders-Belgian population of 215 Parkinson's disease patients as assessed by the Non-Motor Symptoms Questionnaire Wikidata
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study. Wikidata
Non-replication of the brain-derived neurotrophic factor (BDNF) association in bipolar affective disorder: a Belgian patient-control study. Wikidata
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy. Wikidata
Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects. Wikidata
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. Wikidata
novoSNP, a novel computational tool for sequence variation discovery. Wikidata
Parkinson disease: insights in clinical, genetic and pathological features of monogenic disease subtypes. Wikidata
Pathogenesis of polyglutamine disorders: aggregation revisited. Wikidata
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation. Wikidata
Phenotypic variation of autosomal-dominant corticobasal degeneration. Wikidata
Polymorphism of brain derived neurotrophic factor influences β amyloid load in cognitively intact apolipoprotein E ε4 carriers. Wikidata
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis Wikidata
Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Wikidata
Potent amyloidogenicity and pathogenicity of Aβ43. Wikidata
Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models. Wikidata
Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Wikidata
Progress in unraveling the genetic etiology of Parkinson disease in a genomic era. Wikidata
Progressive external ophthalmoplegia characterized by multiple deletions of mitochondrial DNA: unraveling the pathogenesis of human mitochondrial DNA instability and the initiation of a genetic classification. Wikidata
Promoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease. Wikidata
The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects. Wikidata
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration Wikidata
Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort. Wikidata
Reduced hippocampal volume in non-demented carriers of the apolipoprotein E epsilon4: relation to chronological age and recognition memory. Wikidata
Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations. Wikidata
Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin. Wikidata
Relationship between C9orf72 repeat size and clinical phenotype. Wikidata
The role of mutant TAR DNA-binding protein 43 in amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Wikidata
Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Wikidata
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins. Wikidata
Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study. Wikidata
SNPbox: a modular software package for large-scale primer design. Wikidata
SNPbox: web-based high-throughput primer design with an eye for repetitive sequences. Wikidata
SSHSuite: an integrated software package for analysis of large-scale suppression subtractive hybridization data. Wikidata
sTREM2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early-stage Alzheimer's disease and associate with neuronal injury markers. Wikidata
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum. Wikidata
TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies Wikidata
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration Wikidata
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Wikidata
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort Wikidata
Tracing myelin protein zero (P0) in vivo by construction of P0-GFP fusion proteins Wikidata
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis. Wikidata
A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic function. Wikidata
De werking van de hersenen National Library of the Netherlands
De ziekte van Alzheimer National Library of the Netherlands

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