Evidence map›Paper›PMID 35042798›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Integrated genome and transcriptome analyses reveal the mechanism of genome instability in ataxia with oculomotor apraxia 2.

Radhakrishnan Kanagaraj, Richard Mitter, Theodoros Kantidakis, Matthew M Edwards, Anaid Benitez, Probir Chakravarty, Beiyuan Fu, Olivier Becherel, Fengtang Yang, Martin F Lavin and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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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

13 authors at 5 institutions in 3 countries.

Radhakrishnan KanagarajDNA Recombination and Repair Laboratory, The Francis Crick Institute, London NW1 1AT, United Kingdom; drrkanagaraj@gmail.com stephen.west@crick.ac.uk.
Richard MitterBioinformatics and Biostatistics, The Francis Crick Institute, London NW1 1AT, United Kingdom.
Theodoros KantidakisAston Medical School, Aston University, Birmingham B4 7ET, United Kingdom.
Matthew M EdwardsDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853.
Anaid BenitezDNA Recombination and Repair Laboratory, The Francis Crick Institute, London NW1 1AT, United Kingdom.
Probir ChakravartyBioinformatics and Biostatistics, The Francis Crick Institute, London NW1 1AT, United Kingdom.
Beiyuan FuWellcome Sanger Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SA, United Kingdom.
Olivier BecherelCenter for Clinical Research, University of Queensland, Herston, QLD 4029, Australia.
Fengtang YangWellcome Sanger Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SA, United Kingdom.
Martin F LavinCenter for Clinical Research, University of Queensland, Herston, QLD 4029, Australia.
Amnon KorenDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853.
Aengus StewartBioinformatics and Biostatistics, The Francis Crick Institute, London NW1 1AT, United Kingdom.
Stephen C WestDNA Recombination and Repair Laboratory, The Francis Crick Institute, London NW1 1AT, United Kingdom; drrkanagaraj@gmail.com stephen.west@crick.ac.uk.ORCID 0000-0001-8848-9418
The Francis Crick Institute · GBCornell University · USThe University of Queensland · AUWellcome Sanger Institute · GBAston University · GB

Funding

Cancer Research UK 11582Wellcome Trust
6 · The paper itself

Abstract

Mutations in the

Indexed as

AnimalsApraxiasAtaxiaCell LineCerebellar AtaxiaChromosomal InstabilityDNA HelicasesDNA RepairGene Expression ProfilingGenomic InstabilityGenomicsHumansMiceMouse Embryonic Stem CellsMultifunctional EnzymesMutationDNA HelicasesMultifunctional EnzymesRNA HelicasesSETX protein, humanataxia with oculomotor apraxiaDNA repair senataxintranscription stress

Identifiers

PMID35042798
PMCPMC8795503
OpenAlexW4221091066

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.