Evidence map›Paper›PMID 21326321›Full record

ArticleGenes and immunity2011

Two missense variants in UHRF1BP1 are independently associated with systemic lupus erythematosus in Hong Kong Chinese.

Y Zhang, W Yang, C C Mok, T M Chan, R W S Wong, M Y Mok, K W Lee, S N Wong, A M H Leung, T L Lee and 13 more

Abstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 3 pooled it
1.3field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 3 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. The Rare Variant rs35356162 inFrontiers in oncology · 2020
    Article
  8. Review
  9. Article
  10. Advances in lupus genetics and epigenetics.Current opinion in rheumatology · 2014
    Review
  11. Article
  12. Article
  13. Review
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

23 authors at 5 institutions in 2 countries.

Y ZhangDepartment of Paediatrics and Adolescent Medicine, Queen Mary Hospital, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
W Yang
C C Mok
T M Chan
R W S Wong
M Y Mok
K W Lee
S N Wong
A M H Leung
T L Lee
M H K Ho
P P W Lee
W H S Wong
J Yang
J Zhang
C-M Wong
I O L Ng
M-M Garcia-Barceló
S S Cherny
P K-H Tam
P C Sham
C S Lau
Y L Lau
University of Hong Kong · HKQueen Mary Hospital · CNTuen Mun Hospital · CNPamela Youde Nethersole Eastern Hospital · CNQueen Elizabeth Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

UHRF1BP1 encodes a highly conserved protein with unknown function. Previously, a coding variant in this gene was found to be associated with systemic lupus erythematosus (SLE) in populations of European ancestry (rs11755393, R454Q, P=2.22 x 10⁻⁸, odds ratio=1.17). In this study, by a combination of genome-wide study and replication involving a total of 1230 patients and 3144 controls, we confirmed the association of this coding variant to SLE in Hong Kong Chinese. We also identified another coding variant in this gene that independently contributes to SLE susceptibility (rs13205210, M1098T, P=4.44 x 10⁻⁹, odds ratio=1.49). Cross-population confirmation establishes the involvement of this locus in SLE and indicates that distinct alleles are contributing to disease susceptibility.

Indexed as

AllelesAmino Acid SequenceAsian PeopleCCAAT-Enhancer-Binding ProteinsGene FrequencyGene OrderGenetic Predisposition to DiseaseGenome-Wide Association StudyHong KongHumansLinkage DisequilibriumLupus Erythematosus, SystemicMutation, MissensePolymorphism, Single NucleotideUbiquitin-Protein LigasesCCAAT-Enhancer-Binding ProteinsUbiquitin-Protein LigasesUHRF1 protein, human

Identifiers

PMID21326321
OpenAlexW1978449131

What OpenQuestion holds

Textmetadata
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.