Evidence map›Paper›PMID 28977450›Full record

ReviewHuman molecular genetics2017

Pathways to understanding the genomic aetiology of osteoarthritis.

Elena Cibrián Uhalte, Jeremy Mark Wilkinson, Lorraine Southam, Eleftheria Zeggini

Abstract readReview
In one paragraph

Review in Human molecular genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  19. Curcumin Inhibits the PERK-eIF2Oxidative medicine and cellular longevity · 2019
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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

4 authors.

Elena Cibrián UhalteHuman Genetics and Cellular Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1SA, UK.
Jeremy Mark WilkinsonDepartment of Oncology and Metabolism, University of Sheffield, Sheffield, S10 2RX, UK.
Lorraine SouthamWellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
Eleftheria ZegginiHuman Genetics, Wellcome Trust Sanger Institute, Hinxton CB10 1SA, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis is a common, complex disease with no curative therapy. In this review, we summarize current knowledge on disease aetiopathogenesis and outline genetics and genomics approaches that are helping catalyse a much-needed improved understanding of the biological underpinning of disease development and progression.

Indexed as

Disease ProgressionGenomicsHumansOsteoarthritisRisk FactorsSynovial Fluid

Identifiers

PMID28977450
PMCPMC5886472

What OpenQuestion holds

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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.