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List of works by Huw R Morris

A genome-wide association study in multiple system atrophy

scientific article published on 14 September 2016

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

scientific article

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia

scientific article

A novel presenilin 1 mutation, I202F occurring at a previously predicted pathogenic site causing autosomal dominant Alzheimer's disease

scientific article published on 7 December 2010

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

scientific article published on 7 December 2012

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

scientific article published on 13 November 2013

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

scientific article

Analysis of copy number variation using quantitative interspecies competitive PCR

scientific article published on 12 August 2008

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations

article

Aripiprazole associated with severe exacerbation of Parkinson's disease

scientific article published on 01 September 2006

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

Association, expression, pathobiology: is too much tau in PD a blueprint for genetic association?

scientific article published on 01 July 2008

Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology

scientific article

BRain health and healthy AgeINg in retired rugby union players, the BRAIN Study: study protocol for an observational study in the UK.

scientific article published on 26 December 2017

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

scientific article published on July 1, 2012

Case control analysis of repeat expansion size in ataxia

scientific article published on 2 October 2007

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

scientific article published on 16 September 2011

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

scientific article published in January 2010

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

scientific article published on August 2009

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

scientific article published on 3 May 2017

Clinical genetics of familial progressive supranuclear palsy.

scientific article published in July 1999

Clinical grand round: a rapidly progressive pyramidal and extrapyramidal syndrome with a supranuclear gaze palsy

scientific article published in July 2005

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

scientific article published on 12 March 2012

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

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

scientific article

Dentatorubral pallidoluysian atrophy in South Wales.

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

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

scientific article

Distal hereditary motor neuropathy with vocal cord paresis: from difficulty in choral singing to a molecular genetic diagnosis

scientific article published on 19 January 2016

Early Onset Parkinson's Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report

scientific article published on 8 August 2017

Early myoclonic status and outcome after cardiorespiratory arrest

scientific article

Equating scores of the University of Pennsylvania Smell Identification Test and Sniffin' Sticks test in patients with Parkinson's disease

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

Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment

scientific article published on 24 July 2013

Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia

scientific article published on 12 August 2010

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

scientific article

Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates

scientific article published on 16 January 2020

Genetic and phenotypic characterization of complex hereditary spastic paraplegia

scientific article published on 23 May 2016

Genetics of Parkinson's disease

article

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

scientific article published on 15 February 2021

Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease

scientific article published on 28 October 2020

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

scientific article published on 05 June 2017

Hyposmia in progressive supranuclear palsy

scientific article published in April 2010

Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project

scientific article published on 15 September 2020

Is the MC1R variant p.R160W associated with Parkinson's?

scientific article published on 21 September 2015

Late onset startle induced tics

scientific article

Late-onset cytoplasmic body myopathy resembling myotonic dystrophy

scientific article published on 01 June 1999

Multi-modality machine learning predicting Parkinson's disease

scientific article published on 01 April 2022

Mutation in the tau exon 10 splice site region in familial frontotemporal dementia

scientific article published in February 1999

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

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

scientific article

Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patients.

scientific article published on December 2015

Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.

scientific article

Parkinson's disease in GTP cyclohydrolase 1 mutation carriers

scientific article

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

scientific article published on January 2013

Parkinsonism following electrical injury to the hand

scientific article published in May 1998

Parkinson’s families project: a UK-wide study of early onset and familial Parkinson’s disease

scientific article published on 17 October 2024

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

scientific article

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

article

Primary antiphospholipid syndrome presenting as a corticobasal degeneration syndrome

scientific article

Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options

scientific article

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

scientific article published on June 28, 2011

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

scientific article published on 13 May 2011

Recent advances in Parkinson’s disease genetics.

scientific article published on February 2014

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

Repeat expansion disorders

scientific article published on 30 September 2024

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

scientific article

Sensitivity and Specificity of the ECAS in Parkinson's Disease and Progressive Supranuclear Palsy.

scientific article

Sequence analysis of tau in familial and sporadic progressive supranuclear palsy.

scientific article published in March 2002

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

scientific article published on 01 October 2001

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

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

article

The frequency of spinocerebellar ataxia type 23 in a UK population.

scientific article published on 30 October 2012

The genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study.

scientific article published on 6 March 2009

The genetic and pathological classification of familial frontotemporal dementia

scientific article published in November 2001

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

scientific article

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

scientific article published in May 1999

Towards a global view of multiple sclerosis genetics

scientific article published on 8 September 2022

Upbeat nystagmus: clinicoanatomical correlation

scientific article

Use of corticosteroids to suppress drug toxicity in complicated tuberculosis

scientific article published on 01 November 1999

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

scientific article published on 13 August 2012

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

scientific article published on 14 February 2013

Utility of the new Movement Disorder Society clinical diagnostic criteria for Parkinson's disease applied retrospectively in a large cohort study of recent onset cases

scientific article published on 12 April 2017

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

scientific article published on 19 February 2013

Which ante mortem clinical features predict progressive supranuclear palsy pathology?

scientific article published on 13 May 2017

Young onset limb spasticity with PSP-like brain and spinal cord NFT-tau pathology

scientific article

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