User profiles for Andrew Singleton

Andrew Singleton

National Institute on Aging
Verified email at mail.nih.gov
Cited by 128806

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

…, A Rosengren, DS Thelle, A Maria Corsi, A Singleton… - Nature, 2011 - nature.com
Blood pressure is a heritable trait 1 influenced by several biological pathways and responsive
to environmental stimuli. Over one billion people worldwide have hypertension (≥140 mm …

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

…, A Al-Chalabi, CE Shaw, M Tsolaki, AB Singleton… - Nature …, 2009 - nature.com
We undertook a two-stage genome-wide association study (GWAS) of Alzheimer's disease (AD)
involving over 16,000 individuals, the most powerful AD GWAS to date. In stage 1 (3,941 …

[HTML][HTML] Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

…, JF Martı́-Massó, J Pérez-Tur, NW Wood, AB Singleton - Neuron, 2004 - cell.com
Parkinson's disease (PD; OMIM #168600) is the second most common neurodegenerative
disorder in the Western world and presents as a progressive movement disorder. The …

[PDF][PDF] A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

…, SD Pack, A Dutra, E Pak, J Hardy, A Singleton… - Neuron, 2011 - cell.com
The chromosome 9p21 amyotrophic lateral sclerosis-frontotemporal dementia (ALS-FTD)
locus contains one of the last major unidentified autosomal-dominant genes underlying these …

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

…, A Al-Chalabi, CE Shaw, M Tsolaki, AB Singleton… - Nature …, 2011 - nature.com
We sought to identify new susceptibility loci for Alzheimer's disease through a staged
association study (GERAD+) and by testing suggestive loci reported by the Alzheimer's Disease …

Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium

…, S Ramaswamy, OA Ross, DP Salmon, A Singleton… - Neurology, 2017 - AAN Enterprises
The Dementia with Lewy Bodies (DLB) Consortium has refined its recommendations about
the clinical and pathologic diagnosis of DLB, updating the previous report, which has been in …

[HTML][HTML] TREM2 Variants in Alzheimer's Disease

…, P St. George-Hyslop, A Singleton… - … England Journal of …, 2013 - Mass Medical Soc
Background Homozygous loss-of-function mutations in TREM2, encoding the triggering
receptor expressed on myeloid cells 2 protein, have previously been associated with an …

Genome-wide association study reveals genetic risk underlying Parkinson's disease

…, G Deuschl, H Chen, O Riess, JA Hardy, AB Singleton… - Nature …, 2009 - nature.com
We performed a genome-wide association study (GWAS) in 1,713 individuals of European
ancestry with Parkinson's disease (PD) and 3,978 controls. After replication in 3,361 cases …

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

…, EE Eichler, PS Meltzer, SF Nelson, AB Singleton… - science, 2008 - science.org
Schizophrenia is a devastating neurodevelopmental disorder whose genetic influences remain
elusive. We hypothesize that individually rare structural variants contribute to the illness. …

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

…, L Bertram, N Eriksson, T Foroud, AB Singleton - Nature …, 2014 - nature.com
We conducted a meta-analysis of Parkinson's disease genome-wide association studies
using a common set of 7,893,274 variants across 13,708 cases and 95,282 controls. Twenty-six …