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

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

2 Dec 2015

Abstract excerpt

IMPORTANCE: The 16p11.2 BP4-BP5 duplication is the copy number variant most frequently associated with autism spectrum disorder (ASD), schizophrenia, and comorbidities such as decreased body mass index (BMI). OBJECTIVES: To characterize the effects of the 16p11.2 duplication on cognitive, behavioral, medical, and anthropometric traits and to understand the specificity of these effects by systematically comparing...

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder Research
Share to Down syndrome and intellectual disability research
Share to Genomic variations and chromosomal abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 26629640
DOI: 10.1001/jamapsychiatry.2015.2123

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical ComorbiditiesPMID 26629640Read ↗

Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.Semantic proximity Read ↗

The pleiotropic spectrum of proximal 16p11.2 CNVs.Semantic proximity Read ↗

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.Semantic proximity Read ↗

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.Semantic proximity Read ↗

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.Semantic proximity Read ↗

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.Semantic proximity Read ↗

Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome.Semantic proximity Read ↗

Developmental trajectories for young children with 16p11.2 copy number variation.Semantic proximity Read ↗

Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVsSemantic proximity Read ↗

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

Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs.Semantic proximity Read ↗

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

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