Andrew B. Singleton

Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy

A. Singleton, S. Arcuti, G. Logroscino, 2017, Alzheimer's & Dementia.

Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

Sonja W. Scholz, Hannah A. Pliner, John D. Eicher, 2019, Annals of neurology.

Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease.

Janel O. Johnson, D. Hernandez, A. Singleton, 2012, Brain : a journal of neurology.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Fabian J Theis, Andrew D. Johnson, Lorna M. Lopez, 2012, Nature Genetics.

Four novel mutations in the GCH1 gene of Chinese patients with dopa‐responsive dystonia

G. Fénelon, F. Zenasni, H. Houlden, 2010, Movement disorders : official journal of the Movement Disorder Society.

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

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

Title : Establishing the role of rare coding variants in known Parkinson ’ s disease risk loci

T. Price, J. R. Gibbs, S. Lubbe, 2017 .

Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4

C. Blauwendraat, M. Ryten, J. Polke, 2024, Movement disorders : official journal of the Movement Disorder Society.

MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

C. Blauwendraat, B. Boeve, M. Murray, 2024, The Lancet Neurology.

Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation

Luigi Ferrucci, Andrew R. Wood, Tim D. Spector, 2013, PloS one.