Evidence map›Paper›PMID 34551311›Full record

ArticleCell reports2021

Homologous organization of cerebellar pathways to sensory, motor, and associative forebrain.

Thomas J Pisano, Zahra M Dhanerawala, Mikhail Kislin, Dariya Bakshinskaya, Esteban A Engel, Ethan J Hansen, Austin T Hoag, Junuk Lee, Nina L de Oude, Kannan Umadevi Venkataraju and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 2 pooled it
8.5field-weighted citation impact, top 2% 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

91 citing papers in PubMed, 2 syntheses or guidelines pooled it, 127 citations in OpenAlex.

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31 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

15 authors at 5 institutions in 2 countries.

Thomas J PisanoNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Zahra M DhanerawalaNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Mikhail KislinNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Dariya BakshinskayaNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Esteban A EngelNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Ethan J HansenWWAMI Medical Education, University of Idaho, Moscow, ID 83844, USA.
Austin T HoagNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Junuk LeeNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Nina L de OudeDepartment of Neuroscience, Erasmus MC, 3000 DR Rotterdam, the Netherlands.
Kannan Umadevi VenkatarajuCold Spring Harbor Laboratory, One Bungtown Road, Cold Spring Harbor, NY 11724, USA.
Jessica L VerpeutNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA.
Freek E HoebeekDepartment for Developmental Origins of Disease, Brain Center and Wilhelmina Childrens Hospital, University Medical Center Utrecht, Utrecht, the Netherlands.
Ben D RichardsonWWAMI Medical Education, University of Idaho, Moscow, ID 83844, USA; Department of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL 62794, USA.
Henk-Jan BoeleNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA; Department of Neuroscience, Erasmus MC, 3000 DR Rotterdam, the Netherlands. Electronic address: hboele@princeton.edu.
Samuel S-H WangNeuroscience Institute, Washington Road, Princeton University, Princeton, NJ 08544, USA. Electronic address: sswang@princeton.edu.
Princeton University · USUniversity of Idaho · USCold Spring Harbor Laboratory · USErasmus MC · NLUniversity Medical Center Utrecht · NL

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Kenneth A Cornell · 2012 to 2026
$59.8M
Subcortical Neural Coding and DynamicsU19NS104648 · NINDS · PRINCETON UNIVERSITY · PI BRODY, CARLOS D · 2017 to 2021
$15.3M
ResourceP40OD010996 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STRICK, PETER · 2012 to 2024
$11.0M
Imaging adaptive cerebellar processing at cellular resolution in awake miceR01NS045193 · NINDS · PRINCETON UNIVERSITY · PI WANG, SAMUEL SHENG-HUNG · 2003 to 2024
$7.5M
Cerebellar determinants of flexible and social behavior on rapid time scales in autism model mice.R01MH115750 · NIMH · PRINCETON UNIVERSITY · PI PILLOW, JONATHAN WILLIAM, SHAEVITZ, JOSHUA W · 2017 to 2021
$4.7M
A web-based framework for multi-modal visualization and annotation of neuroanatomical dataRF1MH128776 · NIMH · PRINCETON UNIVERSITY · PI KLEINFELD, DAVID, WANG, SAMUEL SHENG-HUNG · 2021 to 2021
$1.6M
Network modulators of auditory thalamocortical feedback inhibitionR21DC018365 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RICHARDSON, BEN D · 2020 to 2022
$443k
Connectivity of the Posterior CerebellumF31NS089303 · NINDS · RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL · PI PISANO, THOMAS JOHN · 2015 to 2020
$231k
NIDCD NIH HHS R21 DC018365NIGMS NIH HHS P20 GM103408NIH HHS P40 OD010996NIMH NIH HHS R01 MH115750NIMH NIH HHS RF1 MH128776NINDS NIH HHS F31 NS089303NINDS NIH HHS R01 NS045193NINDS NIH HHS U19 NS104648
6 · The paper itself

Abstract

Cerebellar outputs take polysynaptic routes to reach the rest of the brain, impeding conventional tracing. Here, we quantify pathways between the cerebellum and forebrain by using transsynaptic tracing viruses and a whole-brain analysis pipeline. With retrograde tracing, we find that most descending paths originate from the somatomotor cortex. Anterograde tracing of ascending paths encompasses most thalamic nuclei, especially ventral posteromedial, lateral posterior, mediodorsal, and reticular nuclei. In the neocortex, sensorimotor regions contain the most labeled neurons, but we find higher densities in associative areas, including orbital, anterior cingulate, prelimbic, and infralimbic cortex. Patterns of ascending expression correlate with c-Fos expression after optogenetic inhibition of Purkinje cells. Our results reveal homologous networks linking single areas of the cerebellar cortex to diverse forebrain targets. We conclude that shared areas of the cerebellum are positioned to provide sensory-motor information to regions implicated in both movement and nonmotor function.

Indexed as

AnimalsCerebellumCerebral CortexFemaleGenetic VectorsMaleMiceMice, Inbred C57BLMice, TransgenicNeural PathwaysProto-Oncogene Proteins c-fosSimplexvirusThalamic NucleiProto-Oncogene Proteins c-foscerebellocorticalcerebellothalamiccorticocerebellarherpes simplexiDISCOlight-sheet microscopynonmotor cerebellumpseudorabiestranssynaptic tracingwhole-brain connectivity

Identifiers

PMID34551311
PMCPMC8506234
OpenAlexW3199687289

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.