Evidence map›Paper›PMID 32719713›Full record

ArticleFrontiers in genetics2020

Independent Replication on Genome-Wide Association Study Signals Identifies

Feixia Zhang, Yong-Fei Wang, Yan Zhang, Zhiming Lin, Yujie Cao, Huoru Zhang, Zhong-Yi Liu, David L Morris, Yujun Sheng, Yong Cui and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Systemic lupus erythematosus as a genetic disease.Clinical immunology (Orlando, Fla.) · 2022
    Article
  9. Review
  10. Lupus Nephritis: Current Perspectives and Moving Forward.Journal of inflammation research · 2022
    Review
  11. Review
  12. Review
  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

15 authors at 7 institutions in 3 countries.

Feixia ZhangDepartment of Pediatrics, Union Hospital Affiliated to Fujian Medical University, Fuzhou, China.
Yong-Fei WangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
Yan ZhangDepartment of Pediatric Surgery, Guangzhou Women and Children's Medical Center, Guangzhou, China.
Zhiming LinDepartment of Rheumatology, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Yujie CaoDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
Huoru ZhangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
Zhong-Yi LiuDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
David L MorrisDivision of Genetics and Molecular Medicine, King's College London, London, United Kingdom.
Yujun ShengDepartment of Dermatology, No.1 Hospital Affiliated to Anhui Medical University, Hefei, China.
Yong CuiDepartment of Dermatology, No.1 Hospital Affiliated to Anhui Medical University, Hefei, China.
Xuejun ZhangDepartment of Dermatology, No.1 Hospital Affiliated to Anhui Medical University, Hefei, China.
Timothy J VyseDivision of Genetics and Molecular Medicine, King's College London, London, United Kingdom.
Yu Lung LauDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
Wanling YangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
Yanhui ChenDepartment of Pediatrics, Union Hospital Affiliated to Fujian Medical University, Fuzhou, China.
University of Hong Kong · HKAnhui Medical University · CNKing's College London · GBFujian Medical University · CNGuangzhou Medical University · CNSun Yat-sen University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a genetically complex autoimmune disease. Despite the significant progress made in identifying susceptibility genes for SLE, the genetic architecture of the disease is far from being understood. In this study, we set to replicate a number of suggestive association signals found in genome-wide association studies (GWASs) in additional independent cohorts. Replication studies were performed on Han Chinese cohorts from Hong Kong and Anhui, involving a total of 2,269 cases and 5,073 controls. We identified a missense variant in

Indexed as

genome-wide association studyIRF3lupus nephritisreplicationsystemic lupus erythematosus

Identifiers

PMID32719713
PMCPMC7348047
OpenAlexW3039800497

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.