Evidence map›Paper›PMID 35857265›Full record

ArticleCerebellum (London, England)2022

The Cerebellar Gene Database: a Collective Database of Genes Critical for Cerebellar Development.

Miguel Ramirez, Joshua Wu, Matthew Liu, Derek Wu, Dave Weeden, Daniel Goldowitz

Open access · hybridAbstract read
In one paragraph

Article in Cerebellum (London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

6 authors at 1 institution in 1 country.

Miguel RamirezCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, 950 W 28th Ave, Vancouver, BC, V6H 3V5, Canada.
Joshua WuCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, 950 W 28th Ave, Vancouver, BC, V6H 3V5, Canada.
Matthew LiuCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, 950 W 28th Ave, Vancouver, BC, V6H 3V5, Canada.
Derek WuCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, 950 W 28th Ave, Vancouver, BC, V6H 3V5, Canada.
Dave WeedenCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, 950 W 28th Ave, Vancouver, BC, V6H 3V5, Canada.
Daniel GoldowitzCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, 950 W 28th Ave, Vancouver, BC, V6H 3V5, Canada. dang@cmmt.ubc.ca.ORCID http://orcid.org/0000-0003-4756-4017
University of British Columbia · CA

Funding

Natural Sciences and Engineering Research Council of Canada AWD #014937
6 · The paper itself

Abstract

This report presents the first comprehensive database that specifically compiles genes critical for cerebellar development and function. The Cerebellar Gene Database details genes that, when perturbed in mouse models, result in a cerebellar phenotype according to available data from both Mouse Genome Informatics and PubMed, as well as references to the corresponding studies for further examination. This database also offers a compilation of human genetic disorders with a cerebellar phenotype and their associated gene information from the Online Mendelian Inheritance in Man (OMIM) database. By comparing and contrasting the mouse and human datasets, we observe that only a small proportion of human mutant genes with a cerebellar phenotype have been studied in mouse knockout models. Given the highly conserved nature between mouse and human genomes, this surprising finding highlights how mouse genetic models can be more frequently employed to elucidate human disease etiology. On the other hand, many mouse genes identified in the present study that are known to lead to a cerebellar phenotype when perturbed have not yet been found to be pathogenic in the cerebellum of humans. This database furthers our understanding of human cerebellar disorders with yet-to-be-identified genetic causes. It is our hope that this gene database will serve as an invaluable tool for gathering background information, generating hypotheses, and facilitating translational research endeavors. Moreover, we encourage continual inputs from the research community in making this compilation a living database, one that remains up-to-date with the advances in cerebellar research.

Indexed as

CerebellumDatabases, GeneticAnimalsDisease Models, AnimalHumansMicePhenotypeCerebellumDatabaseDisordersGenesHumanMouse

Identifiers

PMID35857265
PMCPMC9325837
OpenAlexW4286210803

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.