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

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.

JAMA psychiatry - 1 Mar 2017

Hoeffding Louise K, Trabjerg Betina B, Olsen Line, Mazin Wiktor, Sparsø Thomas, Vangkilde Anders, Mortensen Preben B, Pedersen Carsten B, Werge Thomas

Abstract excerpt

Importance: Microdeletions and duplications have been described at the 22q11.2 locus. However, little is known about the clinical and epidemiologic consequences at the population level. Objective: To identify indicators of deletions or duplications at the 22q11.2 locus and estimate the incidence rate ratios (IRRs) and absolute risk for psychiatric disorders in clinically identified individuals with 22q11.2...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Chromosome Duplication

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 22

Share to Denmark

Share to DiGeorge Syndrome

Share to Mental Disorders

Share to Registries

Share to Schizophrenia

Source

Identifiers

PMID: 28114601
DOI: 10.1001/jamapsychiatry.2016.3939

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.PMID 28114601Read ↗

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.Semantic proximity Read ↗

The Neuropsychiatry of 22q11.2 Deletion Syndrome: An Electronic Health Records StudySemantic proximity Read ↗

The psychiatric phenotypes of 1q21 distal deletion and duplication.Semantic proximity Read ↗

Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: a systematic review of literature and meta-analysis.Semantic proximity Read ↗

[New interdisciplinary S3 guidelines on deletion syndrome 22q11.2, a genetic disease predisposing to neuropsychiatric morbidity].Semantic proximity Read ↗

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical ComorbiditiesSemantic proximity Read ↗

Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion SyndromeSemantic proximity Read ↗

[Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].Semantic proximity Read ↗

Evidence that duplications of 22q11.2 protect against schizophrenia.Semantic proximity Read ↗

Implication of a rare deletion at distal 16p11.2 in schizophrenia.Semantic proximity Read ↗

[22q11.2DS Syndrome as a Genetic Subtype of Schizophrenia].Semantic proximity Read ↗

Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants.Semantic proximity Read ↗

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