Evidence map›Paper›PMID 30619256›Full record

ArticleFrontiers in immunology2018

Novel

João Farela Neves, Rainer Doffinger, Gabriela Barcena-Morales, Catarina Martins, Olivier Papapietro, Vincent Plagnol, James Curtis, Marta Martins, Dinakantha Kumararatne, Ana Isabel Cordeiro and 4 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Case Report:Frontiers in immunology · 2025
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  7. PLCG2 variants in cherubism.The Journal of allergy and clinical immunology · 2024
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  12. Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers.The journal of allergy and clinical immunology. In practice · 2023
    Article
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  15. Article
  16. Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2022
    Article
  17. Review
  18. Article
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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

14 authors at 8 institutions in 4 countries.

João Farela NevesPrimary Immunodeficiencies Unit, Hospital Dona Estefânia-CHLC, EPE, Lisbon, Portugal.
Rainer DoffingerDepartment of Clinical Biochemistry and Immunology, Addenbrooke's Hospital, Cambridge, United Kingdom.
Gabriela Barcena-MoralesLaboratorio de Inmunologia, Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Catarina MartinsCEDOC, Chronic Diseases Research Center, NOVA Medical School, Lisbon, Portugal.
Olivier PapapietroDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
Vincent PlagnolUniversity College London Genetics Institute, University College London, London, United Kingdom.
James CurtisDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
Marta MartinsFaculty of Medicine, University of Lisbon, Lisbon, Portugal.
Dinakantha KumararatneDepartment of Clinical Biochemistry and Immunology, Addenbrooke's Hospital, Cambridge, United Kingdom.
Ana Isabel CordeiroPrimary Immunodeficiencies Unit, Hospital Dona Estefânia-CHLC, EPE, Lisbon, Portugal.
Conceição NevesPrimary Immunodeficiencies Unit, Hospital Dona Estefânia-CHLC, EPE, Lisbon, Portugal.
Luis Miguel BorregoCEDOC, Chronic Diseases Research Center, NOVA Medical School, Lisbon, Portugal.
Matilda KatanStructural and Molecular Biology, Division of Biosciences, University College London, London, United Kingdom.
Sergey NejentsevDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
University of Cambridge · GBAddenbrooke's Hospital · GBHospital de Dona Estefânia · PTUniversidade Nova de Lisboa · PTUniversity College London · GBHospital do Desterro · PTUniversidad Nacional Autónoma de México · MXUniversity of Lisbon · PT

Funding

Medical Research Council MR/M012328/1Medical Research Council MR/P028160/1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Mutation, MissenseAmino Acid SequenceBase SequenceCutis LaxaDNA Mutational AnalysisFemaleHereditary Autoinflammatory DiseasesHumansImmunologic Deficiency SyndromesInfant, NewbornInflammatory Bowel DiseasesMalePedigreePhospholipase C gammaSequence Homology, Amino AcidPhospholipase C gammaAPLAIDauto-inflammatory syndromescutis laxaIL-10IL-1bPLCγ2sensorineural deafness

Identifiers

PMID30619256
PMCPMC6302768
OpenAlexW2905167632

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.