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A common haplotype within the PON1 promoter region is associated with sporadic ALS.
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Polymorphism, Single Nucleotide
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma.
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma.
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types.
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Polymorphism Single Nucleotide