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

In tribute to Bob Blanchard: Divergent behavioral phenotypes of 16p11.2 deletion mice reared in same-genotype versus mixed-genotype cages.

Physiology & behavior - 1 Jul 2015

Yang Mu, Lewis Freeman, Foley Gillian, Crawley Jacqueline N

Abstract excerpt

Mouse models offer indispensable heuristic tools for studying genetic and environmental causes of neuropsychiatric disorders, including autism. Development of useful animal models of complex human behaviors depends not only on extensive knowledge of the human disease, but also on a deep understanding of animal behavior and ethology. Robert and Caroline Blanchard pioneered a number of elegant social paradigms in...

Read the complete abstract on PubMed

Topics

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

Share to Adaptation, Ocular
Share to Chromosomes, Human, Pair 16

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exploratory Behavior

Share to Interpersonal Relations

Share to Maze Learning

Share to Mental Disorders

Share to Recognition, Psychology

Share to Vocalization, Animal

Source

Identifiers

PMID: 26066718
DOI: 10.1016/j.physbeh.2015.04.023

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

In tribute to Bob Blanchard: Divergent behavioral phenotypes of 16p11.2 deletion mice reared in same-genotype versus mixed-genotype cages.PMID 26066718Read ↗

A 16p11.2 deletion mouse model displays quantitatively and qualitatively different behaviours in sociability and social novelty over short- and long-term observationSemantic proximity Read ↗

Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse modelSemantic proximity Read ↗

Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains.Semantic proximity Read ↗

Behavioral Phenotyping for Autism Spectrum Disorders in Mice.Semantic proximity Read ↗

Changes in social behaviour with alterations of MAPK3 and KCTD13/CUL3 pathways in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disordersSemantic proximity Read ↗

Two Novel Mouse Models Mimicking Minor Deletions in 22q11.2 Deletion Syndrome Revealed the Contribution of Each Deleted Region to Psychiatric DisordersSemantic proximity Read ↗

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.Semantic proximity Read ↗

Twenty years of discoveries emerging from mouse models of autism.Semantic proximity Read ↗

Mapping ecologically relevant social behaviours by gene knockout in wild mice.Semantic proximity Read ↗

Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder.Semantic proximity Read ↗

A new twist on behavioral genetics by incorporating wild-derived mouse strains.Semantic proximity Read ↗

Sex-dependent parameters of social behavior show marked variations between distinct laboratory mouse strains and their mixed offspringSemantic proximity Read ↗

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