L. Johnson

An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62‐positive, TDP‐43‐negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline

T. Hortobágyi, A. Al-Chalabi, C. Shaw, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

A. Farmer, P. McGuffin, C. Lewis, 2010, The Lancet Neurology.

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

A. Farmer, P. McGuffin, C. Lewis, 2010, The Lancet Neurology.

Genetically determined variation of respiratory mucins: disease and demography

L. Johnson, 2010 .

Cis‐acting Allelic Variation in MUC5B mRNA Expression is Associated with Different Promoter Haplotypes

D. Swallow, L. Johnson, A. Loh, 2010, Annals of human genetics.

MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort

A. Teixeira, L. Vinall, D. Swallow, 2013, Respirology.

A functional genomics screen identifying blood cell development genes in Drosophila by undergraduates participating in a course-based research experience

Brandon Wei, M. Võ, Mark Douglass, 2021, G3.

The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder

Michelle K. Lupton, T. Hortobágyi, Robert H. Brown, 2012, European Journal of Human Genetics.

Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients

S. Newhouse, A. Al-Chalabi, C. Shaw, 2012, Neurobiology of Aging.

An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62‐positive, TDP‐43‐negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline

T. Hortobágyi, A. Al-Chalabi, C. Troakes, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.