Evidence map›Paper›PMID 30116885›Full record

ReviewMammalian genome : official journal of the International Mammalian Genome Society2018

Human genetics of mycobacterial disease.

Monica Dallmann-Sauer, Wilian Correa-Macedo, Erwin Schurr

Open access · hybridAbstract readReview
In one paragraph

Review in Mammalian genome : official journal of the International Mammalian Genome Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. DiminishedOpen forum infectious diseases · 2025
    Article
  5. Unlocking Opportunities forACS infectious diseases · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Pharmacogenomics and personalized medicine · 2023
    Article
  11. Article
  12. Perspectives for systems biology in the management of tuberculosis.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  13. Article
  14. Impact ofWorld journal of clinical cases · 2020
    Article
  15. Novel Treatments againstAntibiotics (Basel, Switzerland) · 2020
    Review
  16. Human genetics of Buruli ulcer.Human genetics · 2020
    Review
  17. Polymorphisms inFrontiers in genetics · 2020
    Article
  18. Frontiers in immunology · 2020
    Article
  19. Article
  20. Association ofFrontiers in immunology · 2020
    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

3 authors at 1 institution in 1 country.

Monica Dallmann-SauerProgram in Infectious Diseases and Immunity in Global Health, Research Institute, McGill University Health Centre, Montreal, QC, Canada.
Wilian Correa-MacedoProgram in Infectious Diseases and Immunity in Global Health, Research Institute, McGill University Health Centre, Montreal, QC, Canada.
Erwin SchurrProgram in Infectious Diseases and Immunity in Global Health, Research Institute, McGill University Health Centre, Montreal, QC, Canada. erwin.schurr@mcgill.ca.ORCID http://orcid.org/0000-0002-2640-536X
McGill University Health Centre · CA

Funding

CIHR FDN-14332
6 · The paper itself

Abstract

Mycobacterial diseases are caused by members of the genus Mycobacterium, acid-fast bacteria characterized by the presence of mycolic acids within their cell walls. Claiming almost 2 million lives every year, tuberculosis (TB) is the most common mycobacterial disease and is caused by infection with M. tuberculosis and, in rare cases, by M. bovis or M. africanum. The second and third most common mycobacterial diseases are leprosy and buruli ulcer (BU), respectively. Both diseases affect the skin and can lead to permanent sequelae and deformities. Leprosy is caused by the uncultivable M. leprae while the etiological agent of BU is the environmental bacterium M. ulcerans. After exposure to these mycobacterial species, a majority of individuals will not progress to clinical disease and, among those who do, inter-individual variability in disease manifestation and outcome can be observed. Susceptibility to mycobacterial diseases carries a human genetic component and intense efforts have been applied over the past decades to decipher the exact nature of the genetic factors controlling disease susceptibility. While for BU this search was mostly conducted on the basis of candidate genes association studies, genome-wide approaches have been widely applied for TB and leprosy. In this review, we summarize some of the findings achieved by genome-wide linkage, association and transcriptome analyses in TB disease and leprosy and the recent genetic findings for BU susceptibility.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAnimalsBuruli UlcerGenetic LinkageGenome-Wide Association StudyHost-Pathogen InteractionsHumansLeprosyMycobacteriumMycobacterium InfectionsQuantitative Trait LociTuberculosis

Identifiers

PMID30116885
PMCPMC6132723
OpenAlexW2886892293

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.