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 HapMap: charting a course for genetic discovery in neurological diseases.

Archives of neurology - 1 Mar 2008

Hardy John, Singleton Andrew

Abstract excerpt

Whole-genome association analyses have begun to yield confirmed findings for genetic risk variants for complex disease. As the first reports of its application to neurological disease are described, we review this progress, explain the principles of the analysis, and discuss what the future is likely to be in this exciting area.

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Genetic Predisposition to Disease
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nervous System Diseases

Source

Identifiers

PMID: 18332243
DOI: 10.1001/archneur.65.3.319

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The HapMap: charting a course for genetic discovery in neurological diseases.PMID 18332243Read ↗

Genome-wide association studies in neurological disorders.Semantic proximity Read ↗

Mining the genome for susceptibility to complex neurological disorders.Semantic proximity Read ↗

Susceptibility genes and neurological disorders: learning the right lessons from the human genome project.Semantic proximity Read ↗

A HapMap harvest of insights into the genetics of common disease.Semantic proximity Read ↗

Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations.Semantic proximity Read ↗

Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease.Semantic proximity Read ↗

Genetic analysis in neurology: the next 10 years.Semantic proximity Read ↗

Whole genome association studies in complex diseases: where do we stand?Semantic proximity Read ↗

Genetic Architecture of Neurological Disorders and Their Endophenotypes: Insights from Genetic Association Studies.Semantic proximity Read ↗

Neurogenetics II: complex disorders.Semantic proximity Read ↗

Genome-wide association studies in neurology.Semantic 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.