Evidence map›Paper›PMID 30899057›Full record

SynthesisScientific reports2019

Integrative Genome-Wide Association Studies of eQTL and GWAS Data for Gout Disease Susceptibility.

Meng-Tse Gabriel Lee, Tzu-Chun Hsu, Shyr-Chyr Chen, Ya-Chin Lee, Po-Hsiu Kuo, Jenn-Hwai Yang, Hsiu-Hao Chang, Chien-Chang Lee

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  17. Additive Association ofKidney diseases (Basel, Switzerland)
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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

8 authors at 3 institutions in 1 country.

Meng-Tse Gabriel LeeDepartment of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Tzu-Chun HsuDepartment of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Shyr-Chyr ChenDepartment of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Ya-Chin LeeDepartment of Public Health and Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Po-Hsiu KuoDepartment of Public Health and Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Jenn-Hwai YangNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Hsiu-Hao ChangDepartment of Pediatrics, National Taiwan University Hospital, National Taiwan University, College of Medicine, Taipei, Taiwan.
Chien-Chang LeeDepartment of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan. cclee100@gmail.com.
National Taiwan University Hospital · TWNational Taiwan University · TWInstitute of Biomedical Sciences, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a paucity of genome-wide association study on Han Chinese gout patients. We performed a genome-wide association meta-analysis on two Taiwanese cohorts consisting of 758 gout cases and 14166 controls of Han Chinese ancestry. All the participants were recruited from the Taiwan Biobank. For pathway analysis, we applied ICSNPathway (Identify candidate Causal SNPs and Pathways) analysis, and to investigate whether expression-associated genetic variants contribute to gout susceptibility, we systematically integrated lymphoblastoid expression quantitative trait loci (eQTL) and genome-wide association data of gout using Sherlock, a Bayesian statistical frame-work. In the meta-analysis, we found 4 SNPs that reached genome-wide statistical significance (P < 5.0 × 10

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyAdultAgedGenes, RegulatorGoutHumansLinkage DisequilibriumLymphocytesMiddle AgedPolymorphism, Single NucleotideQuantitative Trait LociRisk Factors

Identifiers

PMID30899057
PMCPMC6428872
OpenAlexW2923480041

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.