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12
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD
No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Parkinson's disease and dementia with Lewy bodies: a difference in dose?
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations
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