- Works count
- 701
- Citation count
- 46,061
- H-index
- 102
- i10-index
- 392
Research interests
Publications
Recent advances in the diagnosis and prognosis of amyotrophic lateral sclerosis
The Lancet Neurology · 2022 · 10.1016/s1474-4422(21)00465-8
Emerging insights into the complex genetics and pathophysiology of amyotrophic lateral sclerosis
The Lancet Neurology · 2022 · 10.1016/s1474-4422(21)00414-2
Recent advances in the diagnosis and prognosis of amyotrophic lateral sclerosis
The Lancet Neurology · 2022 · 10.1016/s1474-4422(21)00465-8
A proposal for new diagnostic criteria for ALS
Clinical Neurophysiology · 2020 · 10.1016/j.clinph.2020.04.005
Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
The Lancet Neurology · 2018 · 10.1016/s1474-4422(18)30089-9
Correction: Amyotrophic lateral sclerosis
Nature Reviews Disease Primers · 2017 · 10.1038/nrdp.2017.85
Correction: Amyotrophic lateral sclerosis
Nature Reviews Disease Primers · 2017 · 10.1038/nrdp.2017.85
Amyotrophic lateral sclerosis
Nature Reviews Disease Primers · 2017 · https://doi.org/10.1038/nrdp.2017.71
Detection of long repeat expansions from PCR-free whole-genome sequence data
Genome Research · 2017 · 10.1101/gr.225672.117
Amyotrophic lateral sclerosis: moving towards a new classification system
The Lancet Neurology · 2016 · 10.1016/s1474-4422(16)30199-5
A revision of the El Escorial criteria - 2015
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 2015 · 10.3109/21678421.2015.1049183
Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study
The Lancet Neurology · 2014 · 10.1016/s1474-4422(14)70219-4
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS
Neuron · 2014 · 10.1016/j.neuron.2014.09.027
Controversies and priorities in amyotrophic lateral sclerosis
The Lancet Neurology · 2013 · 10.1016/s1474-4422(13)70036-x
The epidemiology of ALS: a conspiracy of genes, environment and time
Nature Reviews Neurology · 2013 · 10.1038/nrneurol.2013.203
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
The Lancet Neurology · 2012 · 10.1016/s1474-4422(12)70014-5
EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force
European Journal of Neurology · 2011 · https://doi.org/10.1111/j.1468-1331.2011.03501.x
Clinical diagnosis and management of amyotrophic lateral sclerosis
Nature Reviews Neurology · 2011 · 10.1038/nrneurol.2011.153
The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study
Journal of Neurology Neurosurgery & Psychiatry · 2011 · 10.1136/jnnp-2011-300188
Incidence of amyotrophic lateral sclerosis in Europe
Journal of Neurology Neurosurgery & Psychiatry · 2009 · https://doi.org/10.1136/jnnp.2009.183525
Prognostic factors in ALS: A critical review
Amyotrophic Lateral Sclerosis · 2009 · https://doi.org/10.3109/17482960802566824
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
Nature Genetics · 2009 · 10.1038/ng.442
Cognitive impairment in amyotrophic lateral sclerosis
The Lancet Neurology · 2007 · 10.1016/s1474-4422(07)70265-x
Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues
Journal of Neurology Neurosurgery & Psychiatry · 2007 · 10.1136/jnnp.2006.104828
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
Nature Genetics · 2006 · https://doi.org/10.1038/ng1742
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
Neurology · 2006 · 10.1212/01.wnl.0000231510.89311.8b
Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study.
PubMed · 2000 · 10.1001/archneur.57.8.1171
Current projects
No projects listed.