Huw Morris, PhD FRCP
Cardiff, United KingdomResearch field: Medicine - Neurology
Neurogenetics, PD, PSP, FTD, Myoclonus dystonia
Publications
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Journal Article (74)
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Kin Mok, Bryan J. Traynor, Jennifer Schymick et al. (2012) Chromosome 9 ALS and FTD locus is probably derived from a single founder., 209.e3-8. In Neurobiology of aging 33 (1).Download PDF (424.68 KB)
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Javier Simón-Sánchez, Laura L. Kilarski, Michael A. Nalls et al. (2012) Cooperative Genome-Wide Analysis Shows Increased Homozygosity in Early Onset Parkinson's Disease, e28787. In PLoS ONE 7 (3).Download PDF (258.95 KB)
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Elisa Majounie, Alan E Renton, Kin Mok et al. (2012) Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.. In Lancet neurology.
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Huw R Morris, Adrian J Waite, Nigel M Williams et al. (2012) Recent Advances in the Genetics of the ALS-FTLD Complex.. In Current neurology and neuroscience reports.Download PDF (434.58 KB)
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Gavin Charlesworth, Sonia Gandhi, Jose M Bras et al. (2012) Tau acts as an independent genetic risk factor in pathologically proven PD., 838.e7-11. In Neurobiology of aging 33 (4).
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Alan E. Renton, Elisa Majounie, Adrian Waite et al. (2011) A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD, 257-68. In Neuron 72 (2).Download PDF (1.08 MB)
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Alistair Church, Junita Prescott, Suzanne Lillis et al. (2011) A novel presenilin 1 mutation, I202F occurring at a previously predicted pathogenic site causing autosomal dominant Alzheimer's disease. In NEUROBIOLOGY OF AGING 32 (3).
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Vincent Plagnol, Michael A Nalls, Jose M Bras et al. (2011) A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease. In PLOS GENETICS 7 (6).
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(2011) A two-stage meta-analysis identifies several new loci for Parkinson's disease., e1002142. In PLoS genetics 7 (6).Download PDF (425.29 KB)
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Chris C A Spencer, Vincent Plagnol, Amy Strange et al. (2011) Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21., 345-53. In Human molecular genetics 20 (2).Download PDF (205.69 KB)
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