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 Parkinson's Disease Mechanisms and Treatments.
Comprehensive cross-sectional and longitudinal comparisons of plasma glial fibrillary acidic protein and neurofilament light across FTD spectrum disorders
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Support vector machine classification of 18F-FDG PET scans across subtypes of amyotrophic lateral sclerosis
Cellular signatures underlying functional resilience in presymptomatic frontotemporal dementia
Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study
Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohort
Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort
Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia
Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers
Motor symptoms in genetic frontotemporal dementia: developing a new module for clinical rating scales
Cognitive composites for genetic frontotemporal dementia: GENFI-Cog
Language impairment in the genetic forms of behavioural variant frontotemporal dementia
Characterizing the Clinical Features and Atrophy Patterns of <i>MAPT</i> -Related Frontotemporal Dementia With Disease Progression Modeling
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study
Altered levels of CSF proteins in patients with FTD, presymptomatic mutation carriers and non-carriers
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Novel <scp>CSF</scp> biomarkers in genetic frontotemporal dementia identified by proteomics
Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia
Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study
The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference
Poly(GP), neurofilament and grey matter deficits in <i>C9orf72</i> expansion carriers
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study
White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort
Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study