دنبال کردن
Huw R Morris
Huw R Morris
UCL Queen Square Institute of Neurology
ایمیل تأیید شده در ucl.ac.uk
عنوان
نقل شده توسط
نقل شده توسط
سال
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
50352011
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
20892017
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
19992019
Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study
A Varatharaj, N Thomas, MA Ellul, NWS Davies, TA Pollak, EL Tenorio, ...
The Lancet Psychiatry 7 (10), 875-882, 2020
16272020
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
15572018
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
14062012
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
10322011
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium
Science (New York, NY) 360 (6395), eaap8757, 2018
7222018
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), 699-705, 2011
6592011
100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report
100,000 Genomes Project Pilot Investigators
New England Journal of Medicine 385 (20), 1868-1880, 2021
5502021
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
5182000
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
4982001
Visual dysfunction in Parkinson’s disease
RS Weil, AE Schrag, JD Warren, SJ Crutch, AJ Lees, HR Morris
Brain 139 (11), 2827-2843, 2016
4712016
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
4442016
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
4392014
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
4212017
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
3912014
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
3562014
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
3352001
Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms
C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ...
Movement Disorders 34 (6), 866-875, 2019
3332019
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مقاله‌ها 1–20