Evidence map›Paper›PMID 31999079›Full record

ReviewWiley interdisciplinary reviews. Developmental biology2020

FOXP transcription factors in vertebrate brain development, function, and disorders.

Marissa Co, Ashley G Anderson, Genevieve Konopka

Open access · greenAbstract readReview
In one paragraph

Review in Wiley interdisciplinary reviews. Developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 101 citations in OpenAlex.

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6 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Marissa CoDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon.
Ashley G AndersonDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas.
Genevieve KonopkaDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas.ORCID 0000-0002-3363-7302
The University of Texas Southwestern Medical Center · USOregon Health & Science University · US

Funding

Basic Science Training Program in the Neurobiology of Mental IllnessT32MH076690 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI TAMMINGA, CAROL A · 2007 to 2017
$2.3M
The role of Foxp1-regulated signaling pathways in brain development and behaviorR01MH102603 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI KONOPKA, GENEVIEVE · 2015 to 2019
$2.2M
Functional dissection of mammalian vocal communicationR01DC014702 · NIDCD · UT SOUTHWESTERN MEDICAL CENTER · PI KONOPKA, GENEVIEVE · 2016 to 2020
$1.7M
FOXP2-Regulated Signaling Pathways Critical for Higher Cognitive FunctionsR00MH090238 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI KONOPKA, GENEVIEVE · 2011 to 2013
$856k
Mechanisms of Disease & Translational ScienceT32GM109776 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI YIN, HELEN L · 2014 to 2018
$573k
UT Southwestern Center for Translational Medicine (UL18Kl2/TL1)TL1TR001104 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$418k
Genes and Behavior: Reversible Knockdown of FoxP2 in Vocal LearningR21DC016340 · NIDCD · UT SOUTHWESTERN MEDICAL CENTER · PI KONOPKA, GENEVIEVE, ROBERTS, TODD F · 2017 to 2017
$324k
FOXP2-Regulated Signaling Pathways Critical for Higher Cognitive FunctionsK99MH090238 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KONOPKA, GENEVIEVE · 2010 to 2010
$90k
EPA EP-C-15-002NCATS NIH HHS TL1 TR001104NCATS NIH HHS TL1TR001104NIDCD NIH HHS DC014702NIDCD NIH HHS R01 DC014702NIDCD NIH HHS R21 DC016340NIGMS NIH HHS T32 GM109776NIMH NIH HHS K99 MH090238NIMH NIH HHS MH076690NIMH NIH HHS MH090238NIMH NIH HHS MH102603NIMH NIH HHS R00 MH090238NIMH NIH HHS R01 MH102603NIMH NIH HHS T32 MH076690
6 · The paper itself

Abstract

FOXP transcription factors are an evolutionarily ancient protein subfamily coordinating the development of several organ systems in the vertebrate body. Association of their genes with neurodevelopmental disorders has sparked particular interest in their expression patterns and functions in the brain. Here, FOXP1, FOXP2, and FOXP4 are expressed in distinct cell type-specific spatiotemporal patterns in multiple regions, including the cortex, hippocampus, amygdala, basal ganglia, thalamus, and cerebellum. These varied sites and timepoints of expression have complicated efforts to link FOXP1 and FOXP2 mutations to their respective developmental disorders, the former affecting global neural functions and the latter specifically affecting speech and language. However, the use of animal models, particularly those with brain region- and cell type-specific manipulations, has greatly advanced our understanding of how FOXP expression patterns could underlie disorder-related phenotypes. While many questions remain regarding FOXP expression and function in the brain, studies to date have illuminated the roles of these transcription factors in vertebrate brain development and have greatly informed our understanding of human development and disorders. This article is categorized under: Nervous System Development > Vertebrates: General Principles Gene Expression and Transcriptional Hierarchies > Gene Networks and Genomics Nervous System Development > Vertebrates: Regional Development.

Indexed as

AnimalsBrainDevelopmental DisabilitiesForkhead Transcription FactorsGene Expression Regulation, DevelopmentalHumansForkhead Transcription FactorsautismbrainFoxpgene expressiontranscriptional regulation

Identifiers

PMID31999079
PMCPMC8286808
OpenAlexW3003409042

What OpenQuestion 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 OpenQuestion graph.