Elise G.P. Dopper

Erasmus MC — Netherlands

Medicine · Health Sciences

38h-index11.0kcitations108works3.62yr avg
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Research Topics

Amyotrophic Lateral Sclerosis Research(56), Alzheimer's disease research and treatments(40), Dementia and Cognitive Impairment Research(25), Advanced Neuroimaging Techniques and Applications(23), Parkinson's Disease Mechanisms and Treatments(20)

Publications95 total

Distinct proteomic CSF profiles in genetic frontotemporal lobar degeneration
Brain·2025· 1 citedOpen Access
Multiple System Atrophy Without Dysautonomia
Neurology·2025· 1 citedOpen Access
High-resolution in-vivo imaging of glymphatic markers in frontotemporal lobar degeneration using CSF-STREAM at 7 Tesla
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition·2025
Neurochemical changes in presymptomatic C9orf72-HRE frontotemporal lobar degeneration: a 7T magnetic resonance spectroscopy study
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition·2025
Progressive Supranuclear Palsy—A Global Review
Movement Disorders Clinical Practice·2025· 2 cited
Investigating the role of neuroinflammation and brain clearance in frontotemporal lobar degeneration using 7T MRI and fluid biomarkers: protocol for a cross-sectional study in a tertiary care setting
BMJ Open·2025· 2 citedOpen Access
Quantitative MRI-based decision model for early-stage parkinsonism diagnosis: a pilot feasibility study
Neuroimage Reports·2025Open Access
Assessing the Big Five personality traits in presymptomatic and symptomatic C9orf72-related frontotemporal dementia using the Dutch Personality Inventory for DSM-5 (PID-5-NL)
Journal of the Neurological Sciences·2025Open Access
Investigating the Role of Neuroinflammation and Brain Clearance in Frontotemporal Lobar Degeneration using 7T MRI and Biofluid Markers: Protocol for an observational cross-sectional cohort study
2025Open Access
Copy Number Variation and Haplotype Analysis of <scp>17q21.31</scp> Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells
Movement Disorders·2025· 1 citedOpen Access
Montreal Cognitive Assessment vs the Mini-Mental State Examination as a Screening Tool for Patients With Genetic Frontotemporal Dementia
Neurology·2025· 10 citedOpen Access
Fluid and Imaging Markers of Frontotemporal Lobar Degeneration
2025· 1 cited
Two novel variants in GRN: the relevance of CNV analysis and genetic screening in FTLD patients with a negative family history
Journal of Neurology·2024· 2 citedOpen Access
Analysis of Iron Accumulation in MAPT- and C9orf72-associated Frontotemporal Lobar Degeneration: QSM, T2*-w MRI, and Histology
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition·2024
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Molecular Neurodegeneration·2024· 2 citedOpen Access
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Molecular Neurodegeneration·2024· 25 citedOpen Access
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
The American Journal of Human Genetics·2024· 10 citedOpen Access
Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria
Movement Disorders·2024· 11 citedOpen Access
Distinctive cell‐free <scp>DNA</scp> methylation characterizes presymptomatic genetic frontotemporal dementia
Annals of Clinical and Translational Neurology·2024· 6 citedOpen Access
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypes
2024Open Access
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Frequent Co-authors

John C. van Swieten(47), Lize C. Jiskoot(28), Serge A.R.B. Rombouts(24), Yolande A.L. Pijnenburg(22), Lieke Meeter(17), Harro Seelaar(15), Rick van Minkelen(15), Jessica Panman(15), Janne M. Papma(13), Jeroen van der Grond(13), Jonathan D. Rohrer(12), Emma L. van der Ende(12), Barbara Borroni(11), Daniela Galimberti(10), Caroline Graff(10), Jackie M. Poos(10), Anne Hafkemeijer(10), Laura Donker Kaat(10), David M. Cash(9), Robert Laforce(9)