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Authors whose works are in public domain in at least one jurisdiction

List of works by Huw R Morris

1-50 of 102 results

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

scientific article

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

scientific article

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria

scientific article published on 3 May 2017

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

scientific article published on 01 June 2001

Creation of an open-access, mutation-defined fibroblast resource for neurological disease research

scientific article

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

scientific article

Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion

scientific article published on 17 January 2014

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

scientific article published on 13 August 2012

The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK.

scientific article

Chromosome 9 ALS and FTD locus is probably derived from a single founder

scientific article published on 16 September 2011

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

scientific article published on 7 December 2012

Parkinson's disease in GTP cyclohydrolase 1 mutation carriers

scientific article

Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease

scientific article published on 06 September 2012

Genetic and phenotypic characterization of complex hereditary spastic paraplegia

scientific article published on 23 May 2016

The genetic and pathological classification of familial frontotemporal dementia

scientific article published in November 2001

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

scientific article published on 05 June 2017

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.

scientific article published in May 1999

Prevalence and age of onset of Parkinson's disease in Cardiff: a community based cross sectional study and meta-analysis

article

A genome-wide association study in multiple system atrophy

scientific article published on 14 September 2016

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

scientific article

Genetics of Parkinson's disease

article

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

scientific article

C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism

scientific article published on July 1, 2012

Clinical genetics of familial progressive supranuclear palsy.

scientific article published in July 1999

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia

scientific article

Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology

scientific article

Recent advances in Parkinson’s disease genetics.

scientific article published on February 2014

Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation

scientific article

Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing

scientific article published on 30 January 2017

Variation in tau isoform expression in different brain regions and disease states

scientific article published on 19 February 2013

Client and therapist views on exercise programmes for early-mid stage Parkinson's disease and Huntington's disease

scientific article published in January 2010

Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease

scientific article published on 01 October 2000

Which ante mortem clinical features predict progressive supranuclear palsy pathology?

scientific article published on 13 May 2017

Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

scientific article published on 01 October 2001

Parkinson's disease--the debate on the clinical phenomenology, aetiology, pathology and pathogenesis

scientific article published on January 2013

Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance

scientific article

Hyposmia in progressive supranuclear palsy

scientific article published in April 2010

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

scientific article published on 17 May 2017

Early myoclonic status and outcome after cardiorespiratory arrest

scientific article

Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure

scientific article

The effect of age and the H1c MAPT haplotype on MAPT expression in human brain

article

Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: A systematic review.

scientific article published on August 2009

Quality of life in young- compared with late-onset Parkinson's disease

scientific article published on 13 May 2011

Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins

scientific article

Late onset startle induced tics

scientific article

Psychiatric disorders, myoclonus dystonia, and the epsilon‐sarcoglycan gene: A systematic review

scientific article published on June 28, 2011

Parkinson's disease: chameleons and mimics

scientific article published on September 24, 2014

Upbeat nystagmus: clinicoanatomical correlation

scientific article

Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation

scientific article published on February 2004