Evidence map›Paper›PMID 31406627›Full record

ArticleJournal of pediatric genetics2019

The Lebanese Allele in the

Hicham Mansour, Sandra Sabbagh, Sami Bizzari, Stephany El-Hayek, Eliane Chouery, Alicia Gambarini, Martin Gencik, André Mégarbané

Open access · greenAbstract readCase Reports
In one paragraph

Article in Journal of pediatric genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Functions of CytochromeInternational journal of molecular sciences · 2020
    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

8 authors at 5 institutions in 3 countries.

Hicham MansourDepartment of Pediatrics, Saint George Hospital, Beirut, Lebanon.
Sandra SabbaghDepartment Pediatrics, Hotel-Dieu de France, Beirut, Lebanon.
Sami BizzariCentre for Arab Genomic Studies, Dubai, United Arab Emirates.
Stephany El-HayekCentre for Arab Genomic Studies, Dubai, United Arab Emirates.
Eliane ChoueryUnité de Génétique Médicale, Université Saint Joseph, Beirut, Lebanon.
Alicia GambariniInstitut Jérôme Lejeune, CRB BioJeL, Paris, France.
Martin GencikPraxis Fur Humangenetik, Vienna, Austria.
André MégarbanéINOVIE-MENA, Beirut, Lebanon.ORCID 0000-0003-0714-2469
Centre for Arab Genomic Studies · AEFondation Jérôme-Lejeune · FRHôtel-Dieu de France · LBSaint George Hospital · LBSaint Joseph University · LB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytochrome c oxidase deficiency is caused by mutations in any of at least 30 mitochondrial and nuclear genes involved in mitochondrial complex IV biogenesis and structure, including the recently identified

Indexed as

LebanonmitochondriaPET100whole exome sequencing

Identifiers

PMID31406627
PMCPMC6688892
OpenAlexW2939870997

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.