Evidence map›Paper›PMID 35171680›Full record

ArticleScience advances2022

A dominant tubulin mutation causes cerebellar neurodegeneration in a genetic model of tubulinopathy.

Sofia Fertuzinhos, Emilie Legué, Davis Li, Karel F Liem

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Plant direct · 2026
    Article
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  3. Review
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  9. Article
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  11. Tubb4b is required for multi-ciliogenesis in the mouse.Development (Cambridge, England) · 2024
    Article
  12. Culturing Primary Cortical Neurons for Live-Imaging.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  13. Article
  14. Article
  15. 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 1 institution in 1 country.

Sofia FertuzinhosVertebrate Developmental Biology Program, Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520, USA.ORCID 0000-0002-3045-4201
Emilie LeguéVertebrate Developmental Biology Program, Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520, USA.ORCID 0000-0003-0904-2007
Davis LiDepartment of Genetics, Yale University School of Medicine, New Haven, CT 06520, USA.
Karel F LiemVertebrate Developmental Biology Program, Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520, USA.ORCID 0000-0002-1566-5561
Yale University · US

Funding

Genetic Analysis of Mouse Nervous System DevelopmentR01NS044385 · NINDS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI ANDERSON, KATHRYN V · 2002 to 2016
$7.0M
Tubulin Beta 4a in central nervous system development and diseaseR01NS097928 · NINDS · YALE UNIVERSITY · PI LIEM, KAREL F · 2016 to 2020
$2.5M
NINDS NIH HHS R01 NS044385NINDS NIH HHS R01 NS097928
6 · The paper itself

Abstract

Mutations in tubulins cause distinct neurodevelopmental and degenerative diseases termed "tubulinopathies"; however, little is known about the functional requirements of tubulins or how mutations cause cell-specific pathologies. Here, we identify a mutation in the gene

Indexed as

Models, GeneticTubulinCerebellumMicrotubulesMutationTubulin

Identifiers

PMID35171680
PMCPMC8849301
OpenAlexW4213290418

What OpenQuestion holds

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LicenceCC BY-NC
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.