Christine Sato

Brain levels of CDK5 activator p25 are not increased in Alzheimer's or other neurodegenerative diseases with neurofibrillary tangles.

Clinical findings in a large family with a parkin ex3delta40 mutation.

Analysis of the glucocerebrosidase gene in Parkinson's disease.

Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease.

Association studies of cholesterol metabolism genes (CH25H, ABCA1 and CH24H) in Alzheimer's disease.

Association studies between the plasmin genes and late-onset Alzheimer's disease.

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis.

Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics.

LIV-1 ZIP ectodomain shedding in prion-infected mice resembles cellular response to transition metal starvation.

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.

Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism.

Investigation of C9orf72 in 4 Neurodegenerative Disorders.

Segmental duplications in genome-wide significant loci and housekeeping genes; warning for GAPDH and ACTB.

Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion.

Evidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity.

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients.

Mutation analysis of patients with neurodegenerative disorders using NeuroX array.

Identical twins with the C9orf72 repeat expansion are discordant for ALS.

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.

Mutation analysis of CHCHD10 in different neurodegenerative diseases.

Jump from pre-mutation to pathologic expansion in C9orf72.

Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.

Mutation analysis of C9orf72 in patients with corticobasal syndrome.

Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.

Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.

Novel GRN Mutations in Patients with Corticobasal Syndrome.

Mutation analysis of the MS4A and TREM gene clusters in a case-control Alzheimer's disease data set.

Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28.

Drug Repositioning for Alzheimer's Disease Based on Systematic 'omics' Data Mining.

C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism.

DNA methylation age-acceleration is associated with disease duration and age at onset in C9orf72 patients.

The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration.

Unaffected mosaiccase: RNA foci, dipeptide proteins, but upregulated C9orf72 expression.