Huw R Morris
Huw R Morris
UCL Institute of Neurology
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron, 2011
32652011
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
8942012
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
MA Nalls, V Plagnol, DG Hernandez, M Sharma, UM Sheerin, M Saad, ...
Lancet 377 (9766), 641, 2011
8012011
Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria
GU Höglinger, G Respondek, M Stamelou, C Kurz, KA Josephs, AE Lang, ...
Movement Disorders 32 (6), 853-864, 2017
5492017
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
5382018
Differentiation of atypical parkinsonian syndromes with routine MRI
A Schrag, CD Good, K Miszkiel, HR Morris, CJ Mathias, AJ Lees, ...
Neurology 54 (3), 697-697, 2000
4452000
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699, 2011
4252011
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
H Houlden, M Baker, HR Morris, N MacDonald, S Pickering–Brown, ...
Neurology 56 (12), 1702-1706, 2001
4192001
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
2702014
The prevalence of progressive supranuclear palsy (Steele–Richardson–Olszewski syndrome) in the UK
U Nath, Y Ben-Shlomo, RG Thomson, HR Morris, NW Wood, AJ Lees, ...
Brain 124 (7), 1438-1449, 2001
2412001
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion
AJ Waite, D Bäumer, S East, J Neal, HR Morris, O Ansorge, DJ Blake
Neurobiology of aging 35 (7), 1779. e5-1779. e13, 2014
2072014
Frontotemporal dementia and its subtypes: a genome-wide association study
R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ...
The Lancet Neurology 13 (7), 686-699, 2014
2032014
Neurodegeneration: the molecular pathology of dementia and movement disorders
D Dickson, RO Weller
John Wiley & Sons, 2011
1962011
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Human molecular genetics 20 (2), 345-353, 2011
1822011
Loss of VPS13C function in autosomal-recessive Parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
1812016
Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Human molecular genetics 21 (22), 4996-5009, 2012
1732012
A two-stage meta-analysis identifies several new loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium, ...
PLoS Genet 7 (6), e1002142, 2011
1722011
Visual dysfunction in Parkinson’s disease
RS Weil, AE Schrag, JD Warren, SJ Crutch, AJ Lees, HR Morris
Brain 139 (11), 2827-2843, 2016
1632016
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
1622019
A panel of nine cerebrospinal fluid biomarkers may identify patients with atypical parkinsonian syndromes
NK Magdalinou, RW Paterson, JM Schott, NC Fox, C Mummery, ...
Journal of Neurology, Neurosurgery & Psychiatry 86 (11), 1240-1247, 2015
1492015
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