Mahdi Ghani

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

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.

Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohorts.

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.

Mutation analysis of patients with neurodegenerative disorders using NeuroX array.

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

Coding mutations in SORL1 and Alzheimer disease.

Inbreeding among Caribbean Hispanics from the Dominican Republic and its effects on risk of Alzheimer disease.

Mutation analysis of CHCHD10 in different neurodegenerative diseases.

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

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

MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis.

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.

Genetic Variations in ABCA7 Can Increase Secreted Levels of Amyloid-β40 and Amyloid-β42 Peptides and ABCA7 Transcription in Cell Culture Models.

Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations.

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

An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk.