Evidence map›Paper›PMID 30329057›Full record

ArticleHuman molecular genetics2019

A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon.

Carmen Oleaga-Quintas, Caroline Deswarte, Marcela Moncada-Vélez, Ayse Metin, Indumathi Krishna Rao, Saliha Kanik-Yüksek, Alejandro Nieto-Patlán, Antoine Guérin, Belgin Gülhan, Savita Murthy and 8 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Human molecular genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Inherited human IFN-γ deficiency underlies mycobacterial disease.The Journal of clinical investigation · 2020
    Article
  4. Review
  5. A Novel Splice Site Mutation inFrontiers in immunology · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Carmen Oleaga-QuintasLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.
Caroline DeswarteLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.
Marcela Moncada-VélezPrimary Immunodeficiencies Group, School of Medicine, University of Antioquia UdeA, Medellin, Colombia.
Ayse MetinInfectious Diseases Unit, Ankara Hematology Oncology Children's Training and Research Hospital, Ankara, Turkey.
Indumathi Krishna RaoDepartment of Pediatrics, St John's Medical College, Bangalore, India.
Saliha Kanik-YüksekInfectious Diseases Unit, Ankara Hematology Oncology Children's Training and Research Hospital, Ankara, Turkey.
Alejandro Nieto-PatlánLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.
Antoine GuérinLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.
Belgin GülhanInfectious Diseases Unit, Ankara Hematology Oncology Children's Training and Research Hospital, Ankara, Turkey.
Savita MurthyDepartment of Pediatrics, St John's Medical College, Bangalore, India.
Aslinur Özkaya-ParlakayInfectious Diseases Unit, Ankara Hematology Oncology Children's Training and Research Hospital, Ankara, Turkey.
Laurent AbelLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.
Rubén Martínez-BarricarteSt. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, the Rockefeller University, New York, USA.
Rebeca Pérez de DiegoLaboratory of Immunogenetics of Human Diseases IdiPAZ Institute for Health Research, La Paz University Hospital, Madrid, Spain.
Stéphanie Boisson-DupuisLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.
Xiao-Fei KongSt. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, the Rockefeller University, New York, USA.
Jean-Laurent CasanovaLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.
Jacinta BustamanteLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Imagine Institute, Necker Hospital for Sick Children, Paris, France.

Funding

Genome-Wide Dissection of Mendelian Susceptibility to Mycobacterial DiseaseR37AI095983 · NIAID · ROCKEFELLER UNIVERSITY · PI CASANOVA, JEAN-LAURENT · 2011 to 2020
$4.6M
NIAID NIH HHS R37 AI095983
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID30329057
PMCPMC6337693

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.