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One or more keywords matched the following items that are connected to Brown, Robert
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 Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
Academic Article Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
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 Genome-Wide Association Study
Academic Article ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.
Academic Article CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Academic Article Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Academic Article Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden.
Academic Article Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Academic Article A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS.
Academic Article Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
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  • Genome Wide Association Study