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「"Renton AE "[Author]」の検索結果

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A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease.

Empirical design of a variant quality control pipeline for whole genome sequencing data using replicate discordance.

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.

A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data.

C9orf72 hexanucleotide repeat length in older population: normal variation and effects on cognition.

Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.

Melatonin receptor type 1A gene linked to Alzheimer's disease in old age.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten.

The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.

The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.

TBK1 is associated with ALS and ALS-FTD in Sardinian patients.

OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes.

ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry.

A Genome-wide Association Study of Myasthenia Gravis.

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases.

Exploring the epigenetics of Alzheimer disease.

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion.

Genetic architecture of ALS in Sardinia.

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