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 Multiple Sclerosis Research Studies.
Prognostic Factors for Multiple Sclerosis Symptoms in Radiologically Isolated Syndrome
Machine learning in Alzheimer’s disease genetics
Cerebrovascular Reactivity at Rest and Its Association With Cognitive Function in People With Genetic Frontotemporal Dementia
Distinct proteomic CSF profiles in genetic frontotemporal lobar degeneration
Executive Function Deficits in Genetic Frontotemporal Dementia
Thalamus involvement in genetic frontotemporal dementia assessed using structural and diffusion MRI: a GENFI study
Demographic, clinical, biomarker, and neuropathological correlates of posterior cortical atrophy: an international cohort study and individual participant data meta-analysis
Clinical recognition of frontotemporal dementia with right anterior temporal predominance: A multicenter retrospective cohort study
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
Extending the phenotypic spectrum assessed by the CDR plus NACC FTLD in genetic frontotemporal dementia
Mechanism-Free Repurposing of Drugs For C9orf72-related ALS/FTD Using Large-Scale Genomic Data
Mechanism-Free Repurposing of Drugs For C9orf72-Related ALS/FTD Using Large-Scale Genomic Data
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by <i>HLA-DRB1*04</i> subtypes
Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study
Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasia
Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohort
Neuropsychiatric symptoms in genetic frontotemporal dementia: developing a new module for Clinical Rating Scales
Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort
A longitudinal analysis of cerebral blood flow changes in genetic frontotemporal Dementia: Results from genfi
Examining longitudinal changes of disease severity scores in familial forms of frontotemporal dementia within the GENFI cohort
Developing a mass spectrometric assay to measure granulin peptides in CSF for progranulin‐associated frontotemporal dementia
A longitudinal analysis of the frontotemporal dementia rating scale as a sensitive measure of disease trajectory
Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Temporal order of clinical and biomarker changes in familial frontotemporal dementia
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Association of Rare <i>APOE</i> Missense Variants V236E and R251G With Risk of Alzheimer Disease
Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation