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

Parsing psychosis subtypes through investigations of rare genetic variants.

EBioMedicine - 1 Apr 2016

Bergen Sarah E

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to Gene Frequency
Share to Genetic Association Studies
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Models, Genetic

Share to Polymorphism, Single Nucleotide

Share to Psychotic Disorders

Source

Open in PubMed Open full text

Identifiers

PMID: 27211538
DOI: 10.1016/j.ebiom.2016.04.009
PMCID: PMC4856781

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Parsing psychosis subtypes through investigations of rare genetic variants.PMID 27211538Read ↗

Precision medicine for psychotic disorders: objective assessment, risk prediction, and pharmacogenomicsSemantic proximity Read ↗

Rare variants and risk for schizophrenia: more support.Semantic proximity Read ↗

An Investigation of Psychosis Subgroups With Prognostic Validation and Exploration of Genetic Underpinnings: The PsyCourse Study.Semantic proximity Read ↗

Translating Genetic Risk Loci Into Molecular Risk Mechanisms for Schizophrenia.Semantic proximity Read ↗

Phenotypic and genetic complexity of psychosis. Invited commentary on ... Schizophrenia: a common disease caused by multiple rare alleles.Semantic proximity Read ↗

Genetic risk modeling approaches to resolve phenotypic and molecular heterogeneity in psychiatric disorders.Semantic proximity Read ↗

Isolating transdiagnostic effects reveals specific genetic profiles in psychiatric disorders.Semantic proximity Read ↗

Rare variants are common in schizophrenia.Semantic proximity Read ↗

The Psychiatric Genomics Consortium: discoveries and directions.Semantic proximity Read ↗

The Psychiatric Genomics Consortium: Discoveries and DirectionsSemantic proximity Read ↗

The Psychiatric Genomics Consortium: Discoveries and DirectionsSemantic proximity Read ↗

The Psychiatric Genomics Consortium: Discoveries and DirectionsSemantic proximity Read ↗

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