Lauren Johnson

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

Bradley Smith, Stephen Newhouse, Aleksey Shatunov et al. · European Journal of Human Genetics · 2012 · 229 citations · Full text

Amyotrophic Lateral Sclerosis, Genetic Disorder, Genetics +8

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

Aleksey Shatunov, Kin Y. Mok, Stephen Newhouse et al. · The Lancet Neurology · 2010 · 225 citations · Full text

A searchable image resource of Drosophila GAL4 driver expression patterns with single neuron resolution

Geoffrey W Meissner, Aljoscha Nern, Zachary Dorman et al. · eLife · 2023 · 124 citations · Full text

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

Claire Troakes, Satomi Maekawa, Lokesh Wijesekera et al. · Neuropathology · 2011 · 122 citations · Full text

A searchable image resource of <i>Drosophila</i> GAL4-driver expression patterns with single neuron resolution

Geoffrey W Meissner, Aljoscha Nern, Zachary Dorman et al. · 2020 · 24 citations · Full text