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Lieke Meeter

Erasmus MC · NL
Area of research
Neurology · Physiology
Research interest
Research interests include Amyotrophic Lateral Sclerosis Research, Alzheimer's disease research and treatments, Dementia and Cognitive Impairment Research, and Prion Diseases and Protein Misfolding.
h-index
38
citations
5,093
works
83
NIH funding
primary concept
email

Recent publications

Large-scale CSF proteome profiling identifies biomarkers for accurate diagnosis of frontotemporal dementia
Molecular Neurodegeneration 2025cited by 5position: middledoi
CSF proteome profiling across the Alzheimer’s disease spectrum reflects the multifactorial nature of the disease and identifies specific biomarker panels
Nature Aging 2022cited by 98position: middledoi
Elevated CSF and plasma complement proteins in genetic frontotemporal dementia: results from the GENFI study
Journal of Neuroinflammation 2022cited by 36position: middledoi
Cognitive composites for genetic frontotemporal dementia: GENFI-Cog
Alzheimer s Research & Therapy 2022cited by 15position: middledoi
Characterizing the Clinical Features and Atrophy Patterns of <i>MAPT</i> -Related Frontotemporal Dementia With Disease Progression Modeling
Neurology 2021cited by 63position: middledoi
Differential early subcortical involvement in genetic FTD within the GENFI cohort
NeuroImage Clinical 2021cited by 63position: middledoi
A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia
Brain 2021cited by 61position: middledoi
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study
Molecular Neurodegeneration 2021cited by 43position: middledoi
Neuronal pentraxin 2: a synapse-derived CSF biomarker in genetic frontotemporal dementia
Journal of Neurology Neurosurgery & Psychiatry 2020cited by 101position: middledoi
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort
Cortex 2020cited by 49position: middledoi
Diagnostic Value of Cerebrospinal Fluid Neurofilament Light Protein in Neurology
JAMA Neurology 2019cited by 750position: middledoi
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
The Lancet Neurology 2019cited by 303position: middledoi
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
The Lancet Neurology 2019cited by 185position: middledoi
Novel <scp>CSF</scp> biomarkers in genetic frontotemporal dementia identified by proteomics
Annals of Clinical and Translational Neurology 2019cited by 71position: middledoi
Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia
Neurobiology of Aging 2019cited by 65position: middledoi
Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study
Brain 2019cited by 61position: middledoi
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study
NeuroImage Clinical 2019cited by 46position: middledoi
The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint
NeuroImage 2019cited by 43position: middledoi
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference
Nature Communications 2018cited by 567position: middledoi
Poly(GP), neurofilament and grey matter deficits in <i>C9orf72</i> expansion carriers
Annals of Clinical and Translational Neurology 2018cited by 61position: firstdoi
Presymptomatic white matter integrity loss in familial frontotemporal dementia in the <scp>GENFI</scp> cohort: A cross‐sectional diffusion tensor imaging study
Annals of Clinical and Translational Neurology 2018cited by 58position: middledoi
Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort
NeuroImage 2018cited by 23position: middledoi
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study
Neurobiology of Aging 2017cited by 201position: middledoi
White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort
NeuroImage Clinical 2017cited by 80position: middledoi
Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study
Brain 2017cited by 60position: middledoi
Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study
Neurobiology of Aging 2017cited by 57position: middledoi
Neurofilament light chain: a biomarker for genetic frontotemporal dementia
Annals of Clinical and Translational Neurology 2016cited by 265position: firstdoi

Grants

No grants ingested yet.

Frequent collaborators

Yolande A.L. Pijnenburg · University of Lausanne3 papers (2019–2025)John C. van Swieten · Karolinska Institutet3 papers (2019–2025)Daniel Alcolea · Hospital de Sant Pau2 papers (2022–2025)Lisa Vermunt · Erasmus University Rotterdam2 papers (2022–2025) · 2 papers (2022–2025)Alberto Lleó · Instituto de Salud Carlos III2 papers (2022–2025)William T. Hu · Johnson University2 papers (2022–2025)Wiesje M. van der Flier · Alzheimer Nederland2 papers (2022–2025) · 2 papers (2022–2025)Harro Seelaar · University of Massachusetts Chan Medical School2 papers (2019–2025) · 2 papers (2022–2025)Alice Chen‐Plotkin · University of Pennsylvania2 papers (2022–2025)Emma L. van der Ende · Lund University2 papers (2019–2025)Charlotte E. Teunissen · Centrum Wiskunde & Informatica2 papers (2022–2025)David J. Irwin · University of Pennsylvania2 papers (2022–2025) · 1 papers (2022–2022) · 1 papers (2025–2025) · 1 papers (2019–2019)Caroline Graff · Karolinska University Hospital1 papers (2019–2019)Nicholas T. Seyfried · Emory Healthcare1 papers (2022–2022)