Evidence map›Paper›PMID 36750664›Full record

ArticleEuropean journal of human genetics : EJHG2023

Comparing 2D and 3D representations for face-based genetic syndrome diagnosis.

Jordan J Bannister, Matthias Wilms, J David Aponte, David C Katz, Ophir D Klein, Francois P Bernier, Richard A Spritz, Benedikt Hallgrímsson, Nils D Forkert

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Why don't we all use genomic testing?European journal of human genetics : EJHG · 2023
    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

9 authors.

Jordan J BannisterDepartment of Biomedical Engineering, University of Calgary, Calgary, AB, Canada. jordan.bannister@ucalgary.ca.ORCID 0000-0003-1088-5968
Matthias WilmsDepartment of Pediatrics, Department of Community Health Sciences, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.
J David AponteDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, AB, Canada.
David C KatzDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, AB, Canada.
Ophir D KleinProgram in Craniofacial Biology, Department of Orofacial Sciences, University of California, San Francisco, CA, USA.ORCID 0000-0002-6254-7082
Francois P BernierDepartment of Medical Genetics and the Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.
Richard A SpritzDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Benedikt HallgrímssonDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-7192-9103
Nils D ForkertDepartment of Radiology, Alberta Children's Hospital Research Institute, Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada.ORCID 0000-0003-2556-3224

Funding

Developing 3D Craniofacial Morphometry Data and Tools to Transform DysmorphologyU01DE024440 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI HALLGRIMSSON, BENEDIKT, KLEIN, OPHIR D · 2014 to 2018
$3.3M
NIDCR NIH HHS U01 DE024440
6 · The paper itself

Abstract

Human genetic syndromes are often challenging to diagnose clinically. Facial phenotype is a key diagnostic indicator for hundreds of genetic syndromes and computer-assisted facial phenotyping is a promising approach to assist diagnosis. Most previous approaches to automated face-based syndrome diagnosis have analyzed different datasets of either 2D images or surface mesh-based 3D facial representations, making direct comparisons of performance challenging. In this work, we developed a set of subject-matched 2D and 3D facial representations, which we then analyzed with the aim of comparing the performance of 2D and 3D image-based approaches to computer-assisted syndrome diagnosis. This work represents the most comprehensive subject-matched analyses to date on this topic. In our analyses of 1907 subject faces representing 43 different genetic syndromes, 3D surface-based syndrome classification models significantly outperformed 2D image-based models trained and evaluated on the same subject faces. These results suggest that the clinical adoption of 3D facial scanning technology and continued collection of syndromic 3D facial scan data may substantially improve face-based syndrome diagnosis.

Indexed as

FaceImage Processing, Computer-AssistedHumansImaging, Three-DimensionalSyndrome

Identifiers

PMID36750664
PMCPMC10474012

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.