Journal article
A genome-wide association study of sporadic ALS in a homogenous Irish population
Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive limb or bulbar weakness. Efforts to elucidate the disease-associated loci have to date produced conflicting results. One strategy to improve power in genome-wide studies is to genotype a genetically homogenous population. Such a population exhibits extended linkage disequilibrium (LD) and lower allelic heterogeneity to facilitate disease gene …
Authors
Cronin S; Berger S; Ding J; Schymick JC; Washecka N; Hernandez DG; Greenway MJ; Bradley DG; Traynor BJ; Hardiman O
Journal
Human Molecular Genetics, Vol. 17, No. 5, pp. 768–774
Publisher
Oxford University Press (OUP)
Publication Date
March 1, 2008
DOI
10.1093/hmg/ddm361
ISSN
0964-6906
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AgedAllelesAmyotrophic Lateral SclerosisCase-Control StudiesChromosome MappingChromosomes, Human, Pair 7Cohort StudiesDipeptidyl-Peptidases and Tripeptidyl-PeptidasesFemaleGene FrequencyGenetic VariationGenetics, PopulationGenome, HumanHumansIrelandLinkage DisequilibriumLod ScoreMaleMiddle AgedNerve Tissue ProteinsOligonucleotide Array Sequence AnalysisPeptide HydrolasesPolymorphism, Single NucleotidePotassium ChannelsProbabilityStatistics as Topic