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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.
Genome-Wide Association Study
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden.
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS.
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