Jason D. Warren
Researcher Next ID · RN-023696
Researcher · Medicine
University College London Hospitals NHS Foundation Trust
London, Pakistan
- Works count
- 756
- Citation count
- 42,953
- H-index
- 96
- i10-index
- 361
Research interests
Publications
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
The Lancet Neurology · 2019 · https://doi.org/10.1016/s1474-4422(19)30354-0
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
The Lancet Neurology · 2019 · https://doi.org/10.1016/s1474-4422(19)30394-1
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference
Nature Communications · 2018 · https://doi.org/10.1038/s41467-018-05892-0
Prevalence of amyloid‐β pathology in distinct variants of primary progressive aphasia
Annals of Neurology · 2018 · https://doi.org/10.1002/ana.25333
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study
Neurobiology of Aging · 2017 · https://doi.org/10.1016/j.neurobiolaging.2017.10.008
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia
Neurology · 2016 · https://doi.org/10.1212/wnl.0000000000003154
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
The Lancet Neurology · 2015 · 10.1016/s1474-4422(14)70324-2
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions
Acta Neuropathologica · 2014 · https://doi.org/10.1007/s00401-013-1239-x
Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population
The American Journal of Human Genetics · 2013 · https://doi.org/10.1016/j.ajhg.2013.01.011
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Brain · 2011 · https://doi.org/10.1093/brain/awr179
The diagnosis of young-onset dementia
The Lancet Neurology · 2010 · 10.1016/s1474-4422(10)70159-9
The heritability and genetics of frontotemporal lobar degeneration
Neurology · 2009 · 10.1212/wnl.0b013e3181bf997a
Current projects
No projects listed.