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Publications by Christine Van Broeckhoven

Hot-Spot Residue in Small Heat-Shock Protein 22 Causes Distal Motor Neuropathy

Nature Genetics

English

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

American Journal of Human Genetics

English

Human Meiotic Recombination Products Revealed by Sequencing a Hotspot for Homologous Strand Exchange in Multiple HNPP Deletion Patients

American Journal of Human Genetics

English

Tau Is Central in the Genetic Alzheimer–frontotemporal Dementia Spectrum

Trends in Genetics

English

Flemish and Dutch Mutations in Amyloid Β Precursor Protein Have Different Effects on Amyloid Β Secretion

Neurobiology of Disease

English

Apolipoprotein E and Longevity: The Rotterdam Study

Journal of the American Geriatrics Society

English

Serotonin Transporter 5HTTLPR Polymorphism and Affective Disorders: No Evidence of Association in a Large European Multicenter Study

European Journal of Human Genetics

English

A New Locus for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 (CMT2F) Maps to Chromosome 7q11-Q21

European Journal of Human Genetics

English