Michael Owen

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Meta-analysis of the association between variants in SORL1 and Alzheimer disease.

Sandro Sorbi, Masatoshi Takeda, Eng King Tan, 2011, Archives of neurology.

Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Gail Clement, Jie Huang, Inês Barroso, 2016, Nature Communications.

P3-196: A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

Sven Cichon, Carol Brayne, Rebecca Sims, 2008, Alzheimer's & Dementia.

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Taylor J. Maxwell, Peter Holmans, John Hardy, 2006, American journal of human genetics.