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Publications by Christine Van Broeckhoven
Author Correction: Genetic Meta-Analysis of Diagnosed Alzheimer’s Disease Identifies New Risk Loci and Implicates Aβ, Tau, Immunity and Lipid Processing
Nature Genetics
Genetics
Structural Variants Identified by Oxford Nanopore PromethION Sequencing of the Human Genome
Genome Research
Genetics
Loss of DPP6 in Neurodegenerative Dementia: A Genetic Player in the Dysfunction of Neuronal Excitability
Acta Neuropathologica
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
Mutated ATP10B Increases Parkinson’s Disease Risk by Compromising Lysosomal Glucosylceramide Export
Acta Neuropathologica
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
Alpha-Synuclein Repeat Variants and Survival in Parkinson's Disease
Movement Disorders
Neurology
A Pan-European Study of theC9orf72Repeat Associated With FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
Human Mutation
Genetics
Male-Specific Epistasis Between WWC1 and TLN2 Genes Is Associated With Alzheimer’s Disease
Neurobiology of Aging
Aging
Gerontology
Developmental Biology
Geriatrics
Neuroscience
Neurology
Diagnostic Accuracy of Cerebrospinal Fluid Amyloid-Β Isoforms for Early and Differential Dementia Diagnosis
Journal of Alzheimer's Disease
Gerontology
Clinical Psychology
Mental Health
Psychiatry
Geriatrics
Medicine
Neuroscience
Validation of the Erlangen Score Algorithm for Differential Dementia Diagnosis in Autopsy-Confirmed Subjects
Journal of Alzheimer's Disease
Gerontology
Clinical Psychology
Mental Health
Psychiatry
Geriatrics
Medicine
Neuroscience
Peripheral Myelin Protein 2 – A Novel Cluster of Mutations Causing Charcot-Marie-Tooth Neuropathy
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
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