Evidence map›Paper›PMID 35470453›Full record

ArticleThe International journal of eating disorders2022

Bridging the gap: Short structural variants in the genetics of anorexia nervosa.

Natasha Berthold, Julia Pytte, Cynthia M Bulik, Monika Tschochner, Sarah E Medland, Patrick Anthony Akkari

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in The International journal of eating disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 5 institutions in 3 countries.

Natasha BertholdSchool of Nursing, Midwifery, Health Sciences & Physiotherapy, University of Notre Dame Australia, Fremantle, Western Australia, Australia.ORCID 0000-0001-7432-3353
Julia PyttePerron Institute for Neurological and Translational Science, Nedlands, Western Australia, Australia.
Cynthia M BulikDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Monika TschochnerSchool of Nursing, Midwifery, Health Sciences & Physiotherapy, University of Notre Dame Australia, Fremantle, Western Australia, Australia.
Sarah E MedlandQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Patrick Anthony AkkariPerron Institute for Neurological and Translational Science, Nedlands, Western Australia, Australia.
The University of Western Australia · AUDuke University · USQIMR Berghofer Medical Research Institute · AUThe University of Notre Dame Australia · AUUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anorexia nervosa (AN) is a devastating disorder with evidence of underexplored heritability. Twin and family studies estimate heritability (h

Indexed as

Anorexia NervosaCase-Control StudiesCell Adhesion Molecule-1Genetic Predisposition to DiseaseGenome-Wide Association StudyHumansPhenotypePolymorphism, Single NucleotideCADM1 protein, humanCell Adhesion Molecule-1anorexia nervosafeeding and eating disordersgenetic association studiesgenome-wide association studyheritabilitymental disordersmicrosatellite repeats

Identifiers

PMID35470453
PMCPMC9545787
OpenAlexW4224708297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.