Karen E. Morrison

Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene.

D. Lancet, M. Snyder, A. Al-Chalabi, 2021, Cell reports.

Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene

D. Lancet, M. Snyder, J. Landers, 2020, Cell reports.

Establishing the UK DNA Bank for motor neuron disease (MND)

B. Cupid, K. Morrison, P. Shaw, 2015, BMC Genetics.

Telomere length is greater in ALS than in controls: a whole genome sequencing study

Ashley R. Jones, S. Newhouse, J. Powell, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Lateral Sclerosis Degeneration Telomere length is greater in ALS than in controls: a whole genome sequencing study

Ahmad Al Khleifat, Ashley R. Jones, A. Iacoangeli, 2019 .

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Hannah A. Pliner, John D. Eicher, Janel O. Johnson, 2021, JAMA Neurology.