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

Mining the genome for susceptibility to complex neurological disorders.

Current molecular medicine - 1 Sept 2009

Gubitz A K, Gwinn K

Abstract excerpt

Genome-wide association studies (GWAS) have become increasingly widely used to determine regions of the genome which may contain loci influencing the risk of neurological disorders. While linkage studies have identified genes that cause a number of Mendelian disorders, linkage analysis is less well suited for the more common complex disorders. This has led to the widespread use of GWAS for that purpose. Here we...

Read the complete abstract on PubMed

Topics

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

Share to Alzheimer Disease
Share to Amyotrophic Lateral Sclerosis
Share to Genome, Human

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiple Sclerosis

Share to Nervous System Diseases

Share to Parkinson Disease

Share to Restless Legs Syndrome

Share to Supranuclear Palsy, Progressive

Source

Identifiers

PMID: 19860660
DOI: 10.2174/156652409789105534

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

Mining the genome for susceptibility to complex neurological disorders.PMID 19860660Read ↗

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

The HapMap: charting a course for genetic discovery in neurological diseases.Semantic proximity Read ↗

The shared genetic risk architecture of neurological and psychiatric disorders: a genome-wide analysisSemantic proximity Read ↗

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

Genetic association studies of complex neurological diseases.Semantic proximity Read ↗

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

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

Genome-wide association studies: a powerful tool for neurogenomics.Semantic proximity Read ↗

Brain Catalog: a comprehensive resource for the genetic landscape of brain-related traits.Semantic proximity Read ↗

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

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

Genetic approaches to solving common diseases.Semantic proximity Read ↗

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