Evidence map›Paper›PMID 33013854›Full record

ArticleFrontiers in immunology2020

Distinct Clinical Features and Novel Mutations in Taiwanese Patients With X-Linked Agammaglobulinemia.

Yu-Hsin Yeh, Meng-Ying Hsieh, Wen-I Lee, Jing-Long Huang, Li-Chen Chen, Kuo-Wei Yeh, Liang-Shiou Ou, Tsung-Chieh Yao, Chao-Yi Wu, Syh-Jae Lin

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. 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
0.2field-weighted citation impact, top 47% 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, 10 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Revisiting X-linked agammaglobulinemia.Journal of human immunity · 2025
    Review
  10. Inborn Errors of Immunity and Cytokine Storm Syndromes.Advances in experimental medicine and biology · 2024
    Review
  11. Article
  12. Review
  13. Article
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

10 authors at 3 institutions in 1 country.

Yu-Hsin YehDivision of Allergy, Asthma, and Rheumatology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Meng-Ying HsiehDivision of Pediatric Neurology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Wen-I LeeDivision of Allergy, Asthma, and Rheumatology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Jing-Long HuangPrimary Immunodeficiency Care and Research (PICAR) Institute and Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Li-Chen ChenDepartment of Pediatrics, New Taipei Municipal TuChen Hospital, New Taipei City, Taiwan.
Kuo-Wei YehDivision of Allergy, Asthma, and Rheumatology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Liang-Shiou OuDivision of Allergy, Asthma, and Rheumatology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Tsung-Chieh YaoDivision of Allergy, Asthma, and Rheumatology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Chao-Yi WuDivision of Allergy, Asthma, and Rheumatology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Syh-Jae LinDivision of Allergy, Asthma, and Rheumatology, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Chang Gung University · TWChang Gung Memorial Hospital · TWTaipei Municipal YangMing Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdolescentAdultAgammaglobulinaemia Tyrosine KinaseAgammaglobulinemiaChildChild, PreschoolDNA Mutational AnalysisFemaleGenetic Association StudiesGenetic Diseases, X-LinkedHumansInfantMaleMembrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsMutationAgammaglobulinaemia Tyrosine KinaseBTK protein, humanMembrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsTIMM8A protein, humanBruton's tyrosine kinase (BTK)contiguous gene deletion syndrome (CGS)deafness-dystonia-optic neuronopathy syndrome (DDON)Mohr-Tranebjaerg syndrome (MTS)TIMM8A/DDP1 geneX-linked agammaglobulinemia (XLA)

Identifiers

PMID33013854
PMCPMC7498534
OpenAlexW3083429625

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.