Andrew Singleton

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

Sonja W. Scholz, Adriano Chiò, Gabriele Mora, 2007, The Lancet Neurology.

Application of Genome-Wide Single Nucleotide Polymorphism Typing: Simple Association and Beyond

J. Gibbs, J. R. Gibbs, A. Singleton, 2006, PLoS genetics.

A common LRRK2 mutation in idiopathic Parkinson's disease

Nicholas W Wood, Niall P Quinn, Kailash P Bhatia, 2005, The Lancet.

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

Sonja W. Scholz, Scott Silliman, Carl D Langefeld, 2007, The Lancet Neurology.

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

David Heckerman, Lorne Zinman, Joanne Wuu, 2011, Neuron.

Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.

Allissa Dillman, Ronald C Petersen, Mark R Cookson, 2010, American journal of human genetics.

Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation

Vincenzo Bonifati, John Hardy, Peter Heutink, 2003, Annals of neurology.

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

Tatiana Foroud, Nathan Pankratz, Shushant Jain, 2005, The Lancet.