Evidence map›Paper›PMID 36462895›Full record

ArticleArtificial intelligence in medicine2022

Detecting 3D syndromic faces as outliers using unsupervised normalizing flow models.

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

Open access · greenAbstract read
In one paragraph

Article in Artificial intelligence in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Privacy, bias and the clinical use of facial recognition technology: A survey of genetics professionals.American journal of medical genetics. Part C, Seminars in medical genetics · 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 at 3 institutions in 2 countries.

Jordan J BannisterBiomedical Engineering Graduate Program, University of Calgary, Calgary, AB, Canada. Electronic address: jordan.bannister@ucalgary.ca.
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, 2500 University Dr NW, Calgary, AB, Canada.
David C KatzDepartment of Cell Biology and Anatomy, University of Calgary, 2500 University Dr NW, Calgary, AB, Canada.
Ophir D KleinProgram in Craniofacial Biology, Department of Orofacial Sciences, University of California, San Francisco, CA, USA.
Francois P J BernierDepartment of Medical Genetics, 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, 2500 University Dr NW, Calgary, AB, Canada.
Nils D ForkertDepartment of Radiology, Alberta Children's Hospital Research Institute, Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada.
University of Calgary · CAUniversity of California, San Francisco · USUniversity of Colorado Denver · US

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

Many genetic syndromes are associated with distinctive facial features. Several computer-assisted methods have been proposed that make use of facial features for syndrome diagnosis. Training supervised classifiers, the most common approach for this purpose, requires large, comprehensive, and difficult to collect databases of syndromic facial images. In this work, we use unsupervised, normalizing flow-based manifold and density estimation models trained entirely on unaffected subjects to detect syndromic 3D faces as statistical outliers. Furthermore, we demonstrate a general, user-friendly, gradient-based interpretability mechanism that enables clinicians and patients to understand model inferences. 3D facial surface scans of 2471 unaffected subjects and 1629 syndromic subjects representing 262 different genetic syndromes were used to train and evaluate the models. The flow-based models outperformed unsupervised comparison methods, with the best model achieving an ROC-AUC of 86.3% on a challenging, age and sex diverse data set. In addition to highlighting the viability of outlier-based syndrome screening tools, our methods generalize and extend previously proposed outlier scores for 3D face-based syndrome detection, resulting in improved performance for unsupervised syndrome detection.

Indexed as

SyndromeDatabases, FactualHumans3D facial shapeComputer-assisted diagnosisGenetic syndromeNormalizing flowOutlier detection

Identifiers

PMID36462895
PMCPMC10949379
OpenAlexW4306955959

What OpenQuestion holds

Textmetadata
LicenceTDM
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.