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Landers, John
One or more keywords matched the following items that are connected to Landers, John
Item TypeName
Academic Article Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.
Academic Article The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.
Academic Article A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Concept Case-Control Studies
Academic Article Novel mutations support a role for Profilin 1 in the pathogenesis of ALS.
Academic Article NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.
Academic Article Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Academic Article The role of de novo mutations in the development of amyotrophic lateral sclerosis.
Academic Article Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma.
Academic Article Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.
Academic Article Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma.
Academic Article Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Academic Article The Effect of SMN Gene Dosage on ALS Risk and Disease Severity.
Academic Article Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease.
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  • Case Control Studies