to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
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.
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Genetic determinants of amyotrophic lateral sclerosis as therapeutic targets.
Genome-Wide Association Study
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
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.
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
Genome Wide Association Study