Huw R. Morris

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

Janel O. Johnson, D. Hernandez, G. Schellenberg, 2012, The Lancet Neurology.

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

B. Traynor, H. Morris, T. Lynch, 2012, Movement disorders : official journal of the Movement Disorder Society.

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

Mary B Makarious, H. Leonard, D. Vitale, 2023, NPJ Parkinson's disease.

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

D. Hernandez, M. Nalls, A. Singleton, 2013, Human molecular genetics.

Case control analysis of repeat expansion size in ataxia

H. Morris, E. Majounie, W. Cross, 2007, Neuroscience Letters.

Evaluation Of The Rims2 Locus As A Risk Locus For Parkinson's Disease Dementia

M. Shoai, T. Foltynie, M. Lawton, 2021, medRxiv.

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

H. Leonard, D. Knopman, C. van Broeckhoven, 2024, American journal of human genetics.

MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

C. Blauwendraat, B. Boeve, M. Murray, 2024, The Lancet Neurology.