Evidence map›Paper›PMID 32780566›Full record

ArticleCurrent protocols in mouse biology2020

Behavioral Phenotyping for Down Syndrome in Mice.

Randall J Roper, Charles R Goodlett, María Martínez de Lagrán, Mara Dierssen

Open access · greenAbstract read
In one paragraph

Article in Current protocols in mouse biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Sex-specific developmental phenotypes and their response to neonatalbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Randall J RoperIUPUI Department of Biology, Indianapolis, Indiana.
Charles R GoodlettIUPUI Department of Psychology, Indianapolis, Indiana.
María Martínez de LagránCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Mara DierssenCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Indiana University – Purdue University Indianapolis · USCentre for Biomedical Network Research on Rare Diseases · ESCentre for Genomic Regulation · ES

Funding

Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
New methods and theories to interrogate organizational principles from single cell to neuronal networksR01EB028159 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DIERSSEN, MARA, YE, BING · 2019 to 2019
$951k
Development and treatment of skeletal deficits in a Down syndrome mouse modelR15HD090603 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI ROPER, RANDALL J · 2017 to 2020
$900k
CIBERClinical and Translational Sciences AwardCRG Severo Ochoa SEV-2016-0571Indiana Clinical and Translational Sciences Institute UL1TR001108NCATS NIH HHS UL1 TR001108NIBIB NIH HHS R01 EB028159NICHD NIH HHS R15 HD090603NIH HHS 1R01EB 028159-01NIH HHS HD090603Secretaria d'Universitats i Recerca del Departament d'Economia I Coneixement de la Generalitat de Catalunya 2017 SGR 926Spanish Ministry of Science and Innovation and Universities (MSIU)
6 · The paper itself

Abstract

Down syndrome (DS) is the most frequent genetic cause of intellectual disability, characterized by alterations in different behavioral symptom domains: neurodevelopment, motor behavior, and cognition. As mouse models have the potential to generate data regarding the neurological basis for the specific behavioral profile of DS, and may indicate pharmacological treatments with the potential to affect their behavioral phenotype, it is important to be able to assess disease-relevant behavioral traits in animal models in order to provide biological plausibility to the potential findings. The field is at a juncture that requires assessments that may effectively translate the findings acquired in mouse models to humans with DS. In this article, behavioral tests are described that are relevant to the domains affected in DS. A neurodevelopmental behavioral screen, the balance beam test, and the Multivariate Concentric Square Field test to assess multiple behavioral phenotypes and locomotion are described, discussing the ways to merge these findings to more fully understand cognitive strengths and weaknesses in this population. New directions for approaches to cognitive assessment in mice and humans are discussed. © 2020 Wiley Periodicals LLC. Basic Protocol 1: Preweaning neurodevelopmental battery Basic Protocol 2: Balance beam Basic Protocol 3: Multivariate concentric square field test (MCSF).

Indexed as

Behavior Rating ScaleGenetic TechniquesPhenotypeAnimalsDisease Models, AnimalDown SyndromeMaleMicebehavioral phenotypecognitionDown syndromemotor behaviorneurodevelopment

Identifiers

PMID32780566
PMCPMC7552827
OpenAlexW3048715393

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.