Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

21 Sept 2016

Abstract excerpt

Abstract The Ontario Neurodegenerative Disease Research Initiative (ONDRI) is a multimodal, multi-year, prospective observational cohort study to characterise five diseases: (1) Alzheimer’s disease (AD) or amnestic single or multidomain mild cognitive impairment (aMCI) (AD/MCI); (2) amyotrophic lateral sclerosis (ALS); (3) frontotemporal dementia (FTD); (4) Parkinson’s disease (PD); and (5) vascular cognitive...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amyotrophic Lateral Sclerosis Research
Share to Mitochondrial Function and Pathology
Share to Neurological diseases and metabolism

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 29263818
DOI: 10.1038/npjgenmed.2016.32

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegenerationPMID 29263818Read ↗

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.Semantic proximity Read ↗

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.Semantic proximity Read ↗

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases.Semantic proximity Read ↗

Identification And Computational Characterization Of Novel Genetic Variants Associated With Alzheimer's Disease Using Bioinformatics And Machine LearningSemantic proximity Read ↗

Identification And Computational Characterization Of Novel Genetic Variants Associated With Alzheimer's Disease Using Bioinformatics And Machine LearningSemantic proximity Read ↗

Next Generation Sequencing in Alzheimer's Disease.Semantic proximity Read ↗

Data Descriptor: Human whole exome genotype data for Alzheimer’s DiseaseSemantic proximity Read ↗

Whole-Exome Sequencing Analysis of Alzheimer's Disease in Non-APOE*4 Carriers.Semantic proximity Read ↗

Gene panels and primers for next generation sequencing studies on neurodegenerative disordersSemantic proximity Read ↗

NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSemantic proximity Read ↗

The NeuroBioBank Whole-Genome Catalog: Sequencing from human brain donors with central nervous system disordersSemantic proximity Read ↗

NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.